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Artículos de revistas sobre el tema "YnjE"

Autor: Grafiati

Publicado: 4 de junio de 2021

Última modificación: 5 de febrero de 2022

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1

Dahl, Jan-Ulrik, Alexander Urban, Andrea Bolte, et al. "The Identification of a Novel Protein Involved in Molybdenum Cofactor Biosynthesis in Escherichia coli." Journal of Biological Chemistry 286, no. 41 (2011): 35801–12. http://dx.doi.org/10.1074/jbc.m111.282368.

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In the second step of the molybdenum cofactor (Moco) biosynthesis in Escherichia coli, the l-cysteine desulfurase IscS was identified as the primary sulfur donor for the formation of the thiocarboxylate on the small subunit (MoaD) of MPT synthase, which catalyzes the conversion of cyclic pyranopterin monophosphate to molybdopterin (MPT). Although in Moco biosynthesis in humans, the thiocarboxylation of the corresponding MoaD homolog involves two sulfurtransferases, an l-cysteine desulfurase, and a rhodanese-like protein, the rhodanese-like protein in E. coli remained enigmatic so far. Using a

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2

Hänzelmann, Petra, Jan U. Dahl, Jochen Kuper, et al. "Crystal structure of YnjE from Escherichia coli , a sulfurtransferase with three rhodanese domains." Protein Science 18, no. 12 (2009): 2480–91. http://dx.doi.org/10.1002/pro.260.

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3

Rahn-Lee, Lilah, Boris Gorbatyuk, Ole Skovgaard, and Richard Losick. "The Conserved Sporulation Protein YneE Inhibits DNA Replication in Bacillus subtilis." Journal of Bacteriology 191, no. 11 (2009): 3736–39. http://dx.doi.org/10.1128/jb.00216-09.

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ABSTRACT Cells of Bacillus subtilis triggered to sporulate under conditions of rapid growth undergo a marked decrease in chromosome copy number, which was partially relieved by a mutation in the sporulation-induced gene yneE. Cells engineered to express yneE during growth were impaired in viability and produced anucleate cells. We conclude that YneE is an inhibitor of DNA replication.

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4

Schiött, Torbjörn, and Lars Hederstedt. "Efficient Spore Synthesis in Bacillus subtilis Depends on the CcdA Protein." Journal of Bacteriology 182, no. 10 (2000): 2845–54. http://dx.doi.org/10.1128/jb.182.10.2845-2854.2000.

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ABSTRACT CcdA is known to be required for the synthesis ofc-type cytochromes in Bacillus subtilis, but the exact function of this membrane protein is not known. We show that CcdA also plays a role in spore synthesis. The expression of ccdA and the two downstream genesyneI and yneJ was analyzed. There is a promoter for each gene, but there is only one transcription terminator, located after the yneJ gene. The promoter for ccdA was found to be weak and was active mainly during the transition from exponential growth to stationary phase. The promoters foryneI and yneJ were both active in the expon

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5

M, Suresh, and Anchal Yadav. "Knowledge on Breast Cancer among College Students." Young Nurses Journal of Nursing Research 01, no. 01 (2021): 1–4. http://dx.doi.org/10.53926/ynjr/0001.

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Background: Globally, breast cancer is one of the most common cancer among females of age group 15-40 years. India is also one of the leading countries of breast cancer. It is found that incidence rate of breast cancer is higher in less developing countries in comparison to development country. In 2018, worldwide, nearly 2 million new breast cancer cases were diagnosed. Early diagnosis of breast cancer can increase the chance of early case detection and favourable outcomes, resulting in improved survival rates and quality of life of women and is therefore important public health strategy at al

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6

Kavichelvi, K. "Assessment of Effectiveness of Acupressure on Chemotherapy Induced Nausea and Vomiting among Women with Reproductive Organ Cancer." Young Nurses Journal of Research 01, no. 01 (2021): 01–07. http://dx.doi.org/10.53926/ynjr/0002.

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Background of the study: Nausea and vomiting are among the most common and distressing symptoms that patients with cancer endure, both as a result of anti – neoplastic treatment and from the disease itself, and significantly affect patients selfcare, coping abilities, and quality of life. Effective management of these individual symptom's response must be there throughout the cancer treatment. Since the acupressure is an easily applicable method regardless of time and place, cost effective, self-controlled and noninvasive method, it can be used to treat chemotherapy induced nausea and vomiting

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7

Jaspher, M. Justin. "A Comparative Study to Assess the Nutritional Status of Urban and Rural Pre-school Children." Young Nurses Journal of Research 01, no. 01 (2021): 08–13. http://dx.doi.org/10.53926/ynjr/0003.

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Background of the Study: Stunting, wasting, and underweight are the important nutritional status indicators for children. “While stunting is caused by long-term insufficient nutrient intake and repeated infections, wasting is a result of acute food shortage and illness. Wasting, on the other hand, is a strong predictor of mortality and requires urgent response. Underweight combines information about linear growth obstruction and weight for length/height” [7]. Understanding differences in the determinants of childhood malnutrition between urban and rural areas is important to design appropriate

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8

Zaidlewicz, Marek, and Jerzy Meller. "Syntheses with Organoboranes. X. Monohydroboration of Conjugated Enynes with Catecholborane Catalyzed by Nickel(II) Chloride Complexes with Diphosphines." Collection of Czechoslovak Chemical Communications 64, no. 6 (1999): 1049–56. http://dx.doi.org/10.1135/cccc19991049.

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The monohydroboration of representative conjugated enynes - but-1-en-3-yne (1), 2-methylbut-1-en-3-yne (2), pent-3-en-1-yne (3), hex-1-en-3-yne (4), 2-methyl-4-phenylbut-1-en-3-yne (5), 4-methyl-1-phenylpent-3-en-1-yne (6) and 1-ethynylcyclohex-1-ene (7), with catecholborane in the presence of the nickel(II) chloride complex with 1,2-bis(diphenylphosphino)ethane gave the corresponding 1,3-dien-1-yl organoboranes in 54-87% yield. High regioselectivity of the addition leading to the boron atom at the 4-position of the 1-en-3-yne system was observed for 1, 2, 3, 6 and 7.

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9

He, Caigu, Xuehua Zheng, Xiuhong Lin, Xinying Chen, and Chenyi Shen. "Yunvjian-Medicated Serum Protects INS-1 Cells against Glucolipotoxicity-Induced Apoptosis through Autophagic Flux Modulation." Evidence-Based Complementary and Alternative Medicine 2020 (December 14, 2020): 1–15. http://dx.doi.org/10.1155/2020/8878259.

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Yunvjian (YNJ) is a traditional Chinese medicine formula adopted to prevent and treat diabetes. Our previous results from animal experiments showed that YNJ decreased blood glucose. This study aimed to examine the effect of high glucose and high lipid (HG/HL) conditions on the proliferation and apoptosis of INS-1 cells and the possible protective mechanism of YNJ-medicated serum on INS-1 cells exposed to HG/HL conditions. INS-1 cells were cultured in RPMI 1640 medium after being passaged. Then, INS-1 cells in the logarithmic growth phase were collected and divided into five groups: control, HG

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10

Choudhary, Muhammad I., Syed G. Musharraf, Rahat A. Ali, Muhammad Atif та Atta-ur Rahman. "Microbial Transformation of Antifertility Agents, Norethisterone and 17α-Ethynylestradiol". Zeitschrift für Naturforschung B 59, № 3 (2004): 319–23. http://dx.doi.org/10.1515/znb-2004-0314.

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The microbial transformation of oral contraceptive norethisterone (1) by Cephalosporium aphidicola afforded an oxidized metabolite, 17α-ethynylestradiol (2), while the microbial transformation of 2 by Cunninghamella elegans yielded several metabolites, 19-nor-17α-pregna-1,3,5 (10)- trien-20-yne-3,4,17β -triol (3), 19-nor-17α-pregna-1,3,5 (10)-trien-20-yne-3,7α,17β -triol (4), 19- nor-17α-pregna-1,3,5 (10)-trien-20-yne-3,11α,17β -triol (5), 19-nor-17α-pregna-1,3,5 (10)-trien-20- yne-3,6β ,17β -triol (6) and 19-nor-17α-pregna-1,3,5 (10)-trien-20-yne-3,17β -diol-6β -methoxy (7). Metabolite 7 was

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11

Shen, Yechen, and Younghwan Kwon. "Synthesis and Characterization of Reactive Energetic Plasticizers for Poly(glycidyl azide-co-tetramethylene glycol)-Based Polyurethane Binders." Journal of Nanoscience and Nanotechnology 21, no. 7 (2021): 4110–15. http://dx.doi.org/10.1166/jnn.2021.19184.

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Two reactive energetic plasticizers, 3-((2,2-dinitropropoxy)methoxy)prop-1-yne and 4-((2,2-dinitropropoxy)methoxy)but-1-yne which can react with an azido-containing poly(glycidyl azide-co-tetramethylene glycol) prepolymer by cupper-free 1,3-dipolor cycloaddition (“Click”) reaction, were synthesized and characterized, in order to investigate their plasticizing performance and catalyst-free 1,3-dipolar cycloaddition reactivity on energetic polyurethane binders. Two reactive energetic plasticizers showed better plasticizing performance than commercial energetic plasticizers. In the reactivity poi

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12

Banti, Donatella, and Michael North. "Ene-yne-ene and ene-yne-yne metathesis of norbornene derivatives." Tetrahedron Letters 44, no. 44 (2003): 8157–60. http://dx.doi.org/10.1016/j.tetlet.2003.09.035.

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13

Andreica, Adriana Maria, Lucia Gansca, Irina Ciotlaus, and Ioan Oprean. "The Use of Mercury Compounds in the Synthesis of Some Lepidoptera Insect Sex Pheromones with Monoenic Structure." Revista de Chimie 69, no. 6 (2018): 1315–18. http://dx.doi.org/10.37358/rc.18.6.6317.

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New and practical synthesis of (E)-11-tetradecen-1-yl acetate and (Z)-11-hexadecen-1-yl acetate were developed. The synthesis were based on a C12+C2=C14 and C12+C4=C16 coupling scheme. The routes involve, as the key step, the use of the same mercury derivative of the terminal-alkyne w-functionalised as intermediate.The first coupling reaction was effected by adding 1-tert-butoxy-10-bromodecane to monosodate acetylene, obtained in situ from DMSO and sodium hydride. It was prepared 1-tert-butoxy-dodec-11-yne, which is transformed in di[tert-butoxy-dodec-11-yne]mercury, the common intermediate in

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14

Shinde, Mahadev P., Xi Wang, Eun Joo Kang, and Hye-Young Jang. "Platinum-Catalyzed Hydrogenative Cyclization of Yne-Enones, Yne-Aldehydes, and Yne-Dienes." European Journal of Organic Chemistry 2009, no. 35 (2009): 6091–94. http://dx.doi.org/10.1002/ejoc.200901005.

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15

Xia, Ying, Zhen Liu, Rui Ge, Qing Xiao, Yan Zhang, and Jianbo Wang. "Pd-catalyzed cross-coupling of terminal alkynes with ene-yne-ketones: access to conjugated enynes via metal carbene migratory insertion." Chemical Communications 51, no. 56 (2015): 11233–35. http://dx.doi.org/10.1039/c5cc03559g.

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Pd-catalyzed oxidative cross-coupling of terminal alkynes with ene-yne-ketones has been developed, in which the ene-yne-ketones are served as carbene precursors and metal carbene migratory insertion process is the key step for C–C bond formation.

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16

Andreica, Adriana Maria, Lucia Gansca, Irina Ciotlaus, and Ioan Oprean. "Convenient Synthesis of (Z)-7- and (E)-9-dodecene-1-yl Acetate, Components of Some Lepidoptera Insect Sex Pheromone." Revista de Chimie 68, no. 1 (2017): 180–85. http://dx.doi.org/10.37358/rc.17.1.5415.

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Were developed new and practical synthesis of (Z)-7-dodecene-1-yl acetate and (E)-9-dodecene-1-yl acetate. The routes involve, as the key step, the use of the mercury derivative of the terminal-alkyne w-functionalised as intermediate. The synthesis of (Z)-7-dodecene-1-yl acetate was based on a C6+C2=C8 and C8+C4=C12 coupling scheme, starting from 1,6-hexane-diol. The first coupling reaction took place between 1-tert-butoxy-6-bromo-hexane and lithium acetylide-ethylendiamine complex obtaining 1-tert-butoxy-oct-7-yne, which is transformed in di[tert-butoxy-oct-7-yne]mercury. The mercury derivati

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17

Ciotlaus, Irina, Lucia Gansca, Adriana Maria Andreica, and Ioan Oprean. "A Practical Synthesis of (Z)- and (E)-8-Dodecene-1-yl Acetate, Components of Lepidoptera Insect Sex Pheromones." Revista de Chimie 68, no. 1 (2017): 157–62. http://dx.doi.org/10.37358/rc.17.1.5410.

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New and practical synthesis of (Z)-8-dodecene-1-yl acetate and (E)-8-dodecene-1-yl acetate were developed. The synthesis were based on a C3+C6=C9 and C9+C3=C12 coupling scheme, the starting material being 2-propyn-1-ol and 1,6-hexandiol. The routes involve, as the key step, the use of the same mercury derivative of the terminal-alkyne w-functionalised as intermediate. The first coupling reaction took place between methoxyallene and Grignard reagent of 1-tert-butoxy-6-bromo-hexan obtaining 1-tert-butoxy-non-8-yne, which is transformed in di[1-tert-butoxy-non-8-yne]mercury, the common intermedia

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18

Baron, Henry J., and Anne Wadman. "De frou yn'e flesse." World Literature Today 63, no. 4 (1989): 690. http://dx.doi.org/10.2307/40145646.

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19

Baron, Henry J., and Anne Wadman. "In bolle yn'e reak." World Literature Today 61, no. 3 (1987): 455. http://dx.doi.org/10.2307/40143419.

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20

Pineda, Leslie W., María Laura Arias, and Jorge A. Cabezas. "Crystal structures and biological activity of 1,1,4-triphenyl-substituted 1,3-enyne compounds." Acta Crystallographica Section C Structural Chemistry 76, no. 1 (2019): 87–92. http://dx.doi.org/10.1107/s2053229619016127.

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1,3-Enyne structural motifs are versatile building blocks in organic synthesis and occur widely in various natural products with many of them being highly active as cytotoxic macrolides and antitumour antibiotics. This article presents the crystal structure of three 1,1,4-triphenyl-substituted 1,3-enynes, viz. 4-(2-methylphenyl)-1,1-diphenylbut-1-en-3-yne, C23H18 (1), 4-(2-methoxyphenyl)-1,1-diphenylbut-1-en-3-yne, C23H18O (2), and 4-(4-nitrophenyl)-1,1-diphenylbut-1-en-3-yne, C22H15NO2 (3). The benzene ring at position 4 of the but-1-en-3-yne group bears a weakly activating methyl group in co

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21

Reisch, Johannes, and H. Ranjith W. Dharmaratne. "A Convenient Synthesis of the 2-Dimethyl-2H-Chroinene-System." Zeitschrift für Naturforschung B 40, no. 5 (1985): 636–38. http://dx.doi.org/10.1515/znb-1985-0512.

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Abstract 2,2-Dimethyl-5H-pyrano(3,2-c)-l-benzopyrano-5-one(2) and 4H-2,3-dihydro-3-methyl-2-methylene-furan-1-benzopyran-4-one (3), two new coumarin derivatives were synthesised from 4-hydroxycoumarin by treating with 3-chloro-3-methylbut-1-yne and 3-chlorobut-1-yne respectively, both reactions progressing via the phase-transfer catalysis.

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22

Desilva, AN, CL Francis, and AD Ward. "Grignard Addition Reactions to 1,4-Difunctionalized But-2-ynes." Australian Journal of Chemistry 46, no. 11 (1993): 1657. http://dx.doi.org/10.1071/ch9931657.

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Trisubstituted alkenes of E geometry have been prepared by anti addition of Grignard reagents to 1,4-difunctionalized but-2-ynes. Addition of primary, secondary and aromatic Grignard reagents to but-2-yne-1,4-diol provided (E)-2-substituted but-2-ene-1,4-diols as major products along with the corresponding 2-substituted buta-2,3-dien-1-ols. Addition of phenylmagnesium bromide to the mono- and di-methyl ethers of but-2-yne-1,4-diol gave 2,3-diphenyl-1,3-diene. Treatment of 4-dimethylaminobut-2-yn-1-ol with primary alkyl and alkenyl Grignard reagents afforded the 2-substituted anti addition prod

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23

Evano, Gwilherm, and Charles Demmer. "A Simple Entry to Yne-amides from Yne-oxazolidinones." Synlett 27, no. 12 (2016): 1873–77. http://dx.doi.org/10.1055/s-0035-1561976.

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24

Baron, Henry J., and Ypk fan der Fear. "In earme swalker yn'e wrald." World Literature Today 64, no. 1 (1990): 127. http://dx.doi.org/10.2307/40145931.

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25

Andreica, Adriana-Maria, Lucia Gansca, Irina Ciotlaus, and Ioan Oprean. "A New Synthesis of the Sex Pheromone of the Indian Meal Moth Plodia Interpunctella hb. (Lepidoptera, Pyralidae)." Revista de Chimie 71, no. 1 (2020): 201–5. http://dx.doi.org/10.37358/rc.20.1.7832.

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New synthesis of (9Z,12E)-9,12-tetradecadien-1-yl acetate, the sex pheromone of the indian meal moth Plodia interpunctella (Lepidoptera, Pyralidae), were developed. The synthesis was based on a C8+C2=C10 and C10+C4=C14 coupling scheme. The route involves, as the key step, the use of the mercury derivative of the terminal-alkyne -functionalised as intermediate.The first coupling reaction took place between 1-tert-butoxy-8-bromo-octane and lithium acetylide-ethylendiamine complex obtaining 1-tert-butoxy-dec-9-yne, which is transformed in di[tert-butoxy-dec-9-yne]mercury.In the second coupling r

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26

Coll, JC, and AD Wright. "Tropical Marine Algae. IV. Novel Metabolites From the Red Alga Laurencia implicata (Rhodophyta, Rhodophyceae, Ceramiales, Rhodomelaceae)." Australian Journal of Chemistry 42, no. 10 (1989): 1685. http://dx.doi.org/10.1071/ch9891685.

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The marine alga Laurencia implicata afforded four new C15-lipid' type metabolites: (3Z,6Z,9Z)-12-bromo-5,13-epoxypentadeca-3,6,9-trien-1-yne (6) with an unprecedented 1-oxacyclodecane ring, (3Z,6Z,92)-13-bromo-5,12-epoxypentadeca-3,6,9-trien-1-yne (7) with a nine-membered ether ring, (3E,6S,7S,9S,10S,12S,13R)-10,12-dibromo-6,9:7,13-bisepoxy-pentadec-3-en-l-yne (8), in which a chlorine atom in the known compound chlorofucin (9) has been replaced by bromine, (1R*,4R*,6S*,7S*)-9-acetoxy-1,10,12-tribromo-4,7:6,13-bisepoxypentadeca-1,2-diene (11) and the closely related known metabolite neolauralle

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27

Hlavatý, Jaromír, and Miroslav Polášek. "Electrochemical Preparation of Alkynedial Tetramethyl Acetals." Collection of Czechoslovak Chemical Communications 73, no. 1 (2008): 19–23. http://dx.doi.org/10.1135/cccc20080019.

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Tetramethyl acetals of alkynedials were prepared by anodic oxidation of corresponding alkyne-1,ω-diols (C4 and C6) in trimethyl orthoformate on glassy carbone anode in 80% yield. 1,1,4,4-Tetramethoxybut-2-yne (2a) can be prepared by this one-step procedure from but-2-yne-1,4-diol (1a) instead of a multistep chemical procedure starting from 2,5-dimethoxyfuran. Propargyl alcohol (3) can be similarly anodically oxidized in trimethyl orthoformate giving dimethyl acetal of propynal (4) in 85% yield.

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28

Dachs, Anna, Anna Pla-Quintana, Teodor Parella, Miquel Solà, and Anna Roglans. "Intramolecular [2+2+2] Cycloaddition Reactions of Yne-ene-yne and Yne-yne-ene Enediynes Catalysed by RhI: Experimental and Theoretical Mechanistic Studies." Chemistry - A European Journal 17, no. 51 (2011): 14493–507. http://dx.doi.org/10.1002/chem.201102210.

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29

Brener, Nancy D., and Todd W. Wilson. "Substance Use on School Property among Students Attending Alternative High Schools in the United States." Journal of Drug Education 31, no. 4 (2001): 329–42. http://dx.doi.org/10.2190/kqj1-q2fy-ynjc-elb1.

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We analyzed nationally representative data from the 1998 National Alternative High School Youth Risk Behavior Survey, conducted by the Centers for Disease Control and Prevention, to determine the prevalence of substance use on school property among alternative high school students in the United States, to describe the characteristics of students who use substances on school property, and to examine the interrelationships of substance-use behaviors. During the 30 days preceding the survey, nearly 48 percent of students used at least one substance on school property and 17 percent used more than

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30

Peters, Ronald J., Susan R. Tortolero, Robert C. Addy, et al. "The Relationship between Sexual Abuse and Drug Use: Findings from Houston's Safer Choices 2 Program." Journal of Drug Education 33, no. 1 (2003): 49–59. http://dx.doi.org/10.2190/3j7l-yn0e-jaj8-qc6p.

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Self-report drug use data were collected from 282 female alternative school students surveyed through the Safer Choices 2 study in Houston, Texas. Data collection took place between October 2000 and March 2001 via audio-enabled laptop computers equipped with headphones. Logistic regression analyses indicated that sexual abuse history was significantly associated with lifetime use (OR = 1.9, p ≤ 0.05). While the relationships tested in this study are exploratory, they provide evidence for an important connection between sexual abuse and substance use among female alternative school students.

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31

Lin, Xiaofang, Sisi Chen, Weihong Lu, et al. "Diselenide–yne polymerization for multifunctional selenium-containing hyperbranched polymers." Polymer Chemistry 12, no. 23 (2021): 3383–90. http://dx.doi.org/10.1039/d1py00506e.

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32

Dehestani, Maryam, Leila Zeidabadinejad, and Sedigheh Pourestarabadi. "QTAIM investigations of decorated graphyne and boron nitride for Li detection." Journal of the Serbian Chemical Society 82, no. 3 (2017): 289–301. http://dx.doi.org/10.2298/jsc160725012d.

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The interactions between thirteen Li atoms and graphyne (GY) and boron nitride (BN-yne) were investigated by the density functional theory (DFT). The electronic and structural properties of the interactions between the hollow sites of GY and BN-yne with Li atoms were unveiled within the quantum theory of atoms in molecules (QTAIM) framework. Theoretical understanding of the interactions between Li atoms and extended carbon-based network structures is crucial for the development of new materials. Herein, calculations to explore the impact of Li decoration on the GY and BN-yne are reported. It w

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33

Amir, Roey, Assaf Harnoy, Nitsan Papo, and Gadi Slor. "Mixing End Groups in Thiol-Ene/Yne Reactions as a Simple Approach toward Multienzyme-Responsive Polymeric Amphiphiles." Synlett 29, no. 19 (2018): 2582–87. http://dx.doi.org/10.1055/s-0037-1611340.

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Taking advantage of the high fidelity of thiol-ene and thiol-yne chemistries, we used mixtures of thiols to prepare degradable PEG-dendron amphiphiles functionalized with two different types of enzymatically cleavable end groups. By tuning the feed ratios of the two thiols, we achieved mixtures of hybrids with statistically different ratios of end groups. Studies of the disassembly of statistically mixed hybrids showed that these amphiphiles have higher degrees of response when incubated with each of the activating enzymes, whereas a greater degree of selectivity was observed for a control mix

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34

Naher, Masnun, Shawon Shahriar Mehdi, Muhammad Kausar Ahmed, Muhammad Mostafijur Rahman, Mohammad Mizanur Rahman Khan, and Muhammad Younus. "Conjugated Platinum-Poly-Ynes with extended Arylene Ethynylenes." Journal of Bangladesh Academy of Sciences 39, no. 2 (2015): 195–202. http://dx.doi.org/10.3329/jbas.v39i2.25952.

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The platinum-poly-yne polymers poly[trans-bis(tri-n-butylphosphine) platinum-poly (4,4´- diethynylenearylene)] (arylene = biphenylene 3 and anthracene 4) were synthesized by the condensation reaction between poly(diethynylenearylene) (arylene = biphenylene 1 and anthracene 2) and trans-[(PnBu3)2PtCl2] in diisopropyl amine and dichloromethane under nitrogen atmosphere in the presence of CuI catalyst. The newly synthesized platinum containing poly-yne polymers exhibit good solubility in common organic solvents. These metal linked polymers were characterized by IR, 1H NMR and 31P NMR spectroscopy

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35

Bao, Xiucong, Ying Xiong, Xin Li, and Xiang David Li. "A chemical reporter facilitates the detection and identification of lysine HMGylation on histones." Chemical Science 9, no. 40 (2018): 7797–801. http://dx.doi.org/10.1039/c8sc02483a.

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Zhou, Cun Yu, Haoxing Wu, and Neal Krishna Devaraj. "Rapid access to phospholipid analogs using thiol-yne chemistry." Chemical Science 6, no. 7 (2015): 4365–72. http://dx.doi.org/10.1039/c5sc00653h.

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Si, Han, Kaojin Wang, Bo Song, Anjun Qin, and Ben Zhong Tang. "Organobase-catalysed hydroxyl–yne click polymerization." Polymer Chemistry 11, no. 14 (2020): 2568–75. http://dx.doi.org/10.1039/d0py00095g.

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Zhang, Yiru, Jianlei Shen, Rong Hu, et al. "Fast surface immobilization of native proteins through catalyst-free amino-yne click bioconjugation." Chemical Science 11, no. 15 (2020): 3931–35. http://dx.doi.org/10.1039/d0sc00062k.

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Shinde, Mahadev P., Xi Wang, Eun Joo Kang, and Hye-Young Jang. "Platinum-Catalyzed Hydrogenative Cyclization of Yne-Enones, Yne-Aldehydes, and Yne-Dienes (Eur. J. Org. Chem. 35/2009)." European Journal of Organic Chemistry 2009, no. 35 (2009): 6063. http://dx.doi.org/10.1002/ejoc.200990099.

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Escorihuela, Jorge, María-José Bañuls, Rosa Puchades, and Ángel Maquieira. "Site-specific immobilization of DNA on silicon surfaces by using the thiol–yne reaction." J. Mater. Chem. B 2, no. 48 (2014): 8510–17. http://dx.doi.org/10.1039/c4tb01108b.

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Rull-Barrull, J., M. d'Halluin, E. Le Grognec, and F. X. Felpin. "Photoresponsive cellulose paper as a molecular printboard for covalent printing." Journal of Materials Chemistry C 5, no. 21 (2017): 5154–62. http://dx.doi.org/10.1039/c7tc01081h.

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Corcé, Vincent, Lauren McSweeney, Aoife Malone, and Eoin M. Scanlan. "Intramolecular thiol–yne cyclisation as a novel strategy for thioglycal synthesis." Chemical Communications 51, no. 41 (2015): 8672–74. http://dx.doi.org/10.1039/c5cc02162f.

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Weingand, Vanessa, Thomas Wurm, Vanessa Vethacke, et al. "Intermolecular Desymmetrizing Gold-Catalyzed Yne-Yne Reaction of Push-Pull Diarylalkynes." Chemistry - A European Journal 24, no. 15 (2018): 3725–28. http://dx.doi.org/10.1002/chem.201800360.

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Berger, Martin, Yong Chen, Konstantina Bampali, Margot Ernst, and Nuno Maulide. "Expeditious synthesis of polyacetylenic water hemlock toxins and their effects on the major GABAA receptor isoform." Chemical Communications 54, no. 16 (2018): 2008–11. http://dx.doi.org/10.1039/c7cc09801d.

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He, Benzhao, Shijie Zhen, Yongwei Wu, et al. "Cu(i)-Catalyzed amino-yne click polymerization." Polymer Chemistry 7, no. 48 (2016): 7375–82. http://dx.doi.org/10.1039/c6py01501h.

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Burykina, Julia V., Nikita S. Shlapakov, Evgeniy G. Gordeev, Burkhard König, and Valentine P. Ananikov. "Selectivity control in thiol–yne click reactions via visible light induced associative electron upconversion." Chemical Science 11, no. 37 (2020): 10061–70. http://dx.doi.org/10.1039/d0sc01939a.

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Kulkarni, Bhimashnkar A., Angshuman Chattopadhyay, and Vasant R. Mamdapur. "A Brief Synthesis of 3-Hydroxyeicos-4(E)-en-1-yne, a Component of Marine Sponge, Cribrochalina vasculum." Collection of Czechoslovak Chemical Communications 58, no. 7 (1993): 1711–13. http://dx.doi.org/10.1135/cccc19931711.

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Hartlieb, Matthias, Thomas Floyd, Alexander B. Cook, et al. "Well-defined hyperstar copolymers based on a thiol–yne hyperbranched core and a poly(2-oxazoline) shell for biomedical applications." Polymer Chemistry 8, no. 13 (2017): 2041–54. http://dx.doi.org/10.1039/c7py00303j.

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Cai, Xiao Yan, Jun Zhi Li, Ning Ning Li, Jiu Cun Chen, En-Tang Kang, and Li Qun Xu. "PEG-based hydrogels prepared by catalyst-free thiol–yne addition and their post-antibacterial modification." Biomaterials Science 4, no. 11 (2016): 1663–72. http://dx.doi.org/10.1039/c6bm00395h.

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Ballarin, Barbara, Davide Barreca, Elisa Boanini, et al. "Functionalization of silica through thiol-yne radical chemistry: a catalytic system based on gold nanoparticles supported on amino-sulfide-branched silica." RSC Advances 6, no. 31 (2016): 25780–88. http://dx.doi.org/10.1039/c6ra02479c.

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