Log in

Relevant bibliographies by topics / Ring formation (Chemistry) Diels-Alder reaction. Organic compounds / Journal articles

To see the other types of publications on this topic, follow the link: Ring formation (Chemistry) Diels-Alder reaction. Organic compounds.

Journal articles on the topic 'Ring formation (Chemistry) Diels-Alder reaction. Organic compounds'

Author: Grafiati

Published: 4 June 2021

Last updated: 11 February 2022

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 29 journal articles for your research on the topic 'Ring formation (Chemistry) Diels-Alder reaction. Organic compounds.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Tietze, Lutz F., Christian Ott, and Frank Haunert. "Efficient and regioselective synthesis of bridged ring systems by domino Knoevenagel hetero-DielsAlder reaction." Canadian Journal of Chemistry 79, no. 11 (2001): 1511–14. http://dx.doi.org/10.1139/v00-204.

Full text

Abstract:

The bridged heterocycles 1012 were efficiently prepared by a domino Knoevenagel hetero-DielsAlder reaction of N,N'-dimethylbarbituric acid 2 and the aldehydes 68 which contain an allyl moiety as dienophile. In contrast, reaction of 2 and aldehyde 5 with a dimethylallyl moiety leads to the annulated product 9. For the formation of 1012, an exo-Z-syn and for that of 9 an endo-E-syn transition structure is proposed.Key words: bridged compounds, domino reaction, DielsAlder reaction, heterocycles, Knoevenagel reaction.

APA, Harvard, Vancouver, ISO, and other styles

2

Xu, Yao-Chang, Michel Cantin, and Pierre Deslongchamps. "Stereocontrolled construction of A.B.C.[6.6.6] tricycle via transannular Diels–Alder reaction of 14-membered macrocycle with acetylene as dienophile." Canadian Journal of Chemistry 68, no. 12 (1990): 2137–43. http://dx.doi.org/10.1139/v90-328.

Full text

Abstract:

The syntheses of the acyclic dienynes 14a (cis-trans-acetylene) and 14b (trans-trans-acetylene) are described. The tandem macrocyclization and transannular Diels–Alder reaction of the allylic chloride 14b was conducted in the presence of Cs2CO3 at 85 °C in one-pot to provide tricyclic product 16, with the two hydrogens in ring B being cis. On the other hand, treatment of the allylic chloride 14a under the same conditions afforded 14-membered macrocycle 17, which could be transformed at 250 °C into a similar tricyclic product 18 with the two hydrogens in ring B being trans, along with an intere

APA, Harvard, Vancouver, ISO, and other styles

3

Virolleaud, Marie-Alice, and Olivier Piva. "Tandem Sequential Ring-Closing Metathesis/Diels–Alder/Cross-Metathesis: Formation of Polycyclic Compounds by a New Three-Component Reaction." European Journal of Organic Chemistry 2007, no. 10 (2007): 1606–12. http://dx.doi.org/10.1002/ejoc.200600946.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Back, Thomas G. "Design and synthesis of some biologically interesting natural and unnatural products based on organosulfur and selenium chemistry." Canadian Journal of Chemistry 87, no. 12 (2009): 1657–74. http://dx.doi.org/10.1139/v09-133.

Full text

Abstract:

Organosulfur and selenium chemistry has provided fertile ground for the discovery of novel synthetic methodology and for the design of bioactive molecules with potential therapeutic applications. Thus, acetylenic sulfones have been employed in novel strategies for the synthesis of nitrogen heterocycles, including several biologically active alkaloids. The conjugate addition of nitrogen nucleophiles containing ester or chloroalkyl substituents to acetylenic sulfones was followed by base-mediated intramolecular alkylation or acylation to afford variously substituted piperidines, pyrrolizidines,

APA, Harvard, Vancouver, ISO, and other styles

5

Patel, H. S., and V. C. Patel. "Polyimides Containing an s-Triazine Ring." High Performance Polymers 12, no. 1 (2000): 225–35. http://dx.doi.org/10.1088/0954-0083/12/1/319.

Full text

Abstract:

A series of new polyimides containing an s-triazine nucleus were prepared via Diels–Alder (DA) intermolecular polymerization of 2,6-bis(2-furanyl methyl imino)-4-ethoxy-1,3,5-triazine with different bis(maleimide) compounds. The DA reaction was carried out in tetrahydrofuran as solvent, as well as in bulk followed by aromatization of poly(tetrahydrophthalimido)-intermediates in the presence of acetic anhydride. All the poly(imino- s-triazine imide)s were characterized by elemental analysis, IR spectral studies and thermogravimetry. Glass fibre reinforced composites were prepared via in situ Di

APA, Harvard, Vancouver, ISO, and other styles

6

Padwa, Albert, William S. Kissell, and Cheryl K. Eidell. "Cyclizationcycloaddition cascades for the construction of azapolycyclic ring systems." Canadian Journal of Chemistry 79, no. 11 (2001): 1681–93. http://dx.doi.org/10.1139/v01-154.

Full text

Abstract:

Cyclic 2-amidofuranones were obtained from the Rh(II)-catalyzed reaction of alpha-diazoketo substituted pyrrolidine derivatives. These compounds are derived by a [1,4]-hydrogen transfer from an initially formed carbonyl ylide dipole. Acylation of the amido-substituted furanone with pivalyl chloride provided a fused amidofuran, which underwent bimolecular Diels-Alder cycloaddition with N-phenylmaleimide. The Rh(II)-catalyzed decomposition of ethyl 2-diazo-3-oxo-(2-oxo-1-pent-4-enoyl-pyrrolidine-3-yl)propionate was also examined. In this case, the alkenyl group tethered to the amido carbonyl und

APA, Harvard, Vancouver, ISO, and other styles

7

Kotha, Sambasivarao, Saidulu Todeti, and Vikas R. Aswar. "Design and synthesis of C 3-symmetric molecules bearing propellane moieties via cyclotrimerization and a ring-closing metathesis sequence." Beilstein Journal of Organic Chemistry 14 (October 1, 2018): 2537–44. http://dx.doi.org/10.3762/bjoc.14.230.

Full text

Abstract:

We have developed an efficient synthetic strategy to assemble C 3-symmetric molecules containing propellane moieties as end groups and a benzene ring as a central core. The synthesis of these C 3-symmetric molecules involves simple starting materials. Our approach to C 3-symmetric compounds relies on a Diels–Alder reaction, cyclotrimerization and ring-closing metathesis as key steps.

APA, Harvard, Vancouver, ISO, and other styles

8

Palkó, Márta, Mohamed El Haimer, Zsanett Kormányos, and Ferenc Fülöp. "Synthesis of Novel N-Heterocyclic Compounds Containing 1,2,3-Triazole Ring System via Domino, “Click” and RDA Reactions." Molecules 24, no. 4 (2019): 772. http://dx.doi.org/10.3390/molecules24040772.

Full text

Abstract:

An uncomplicated, high-yielding synthetic route has been developed to constitute complicated heterocycles, applying domino, click and retro-Diels–Alder (RDA) reaction sequences. Starting from 2-aminocarboxamides, a new set of isoindolo[2,1-a]quinazolinones was synthesized with domino ring closure. A click reaction was performed to create the 1,2,3-triazole heterocyclic ring, followed by an RDA reaction resulting in dihydropyrimido[2,1-a]isoindole-2,6-diones. The absolute configuration, concluded by the norbornene structure that served as a chiral source, remained constant throughout the transf

APA, Harvard, Vancouver, ISO, and other styles

9

Nakada, Masahisa, Hiroki Shimoda, Takahiro Shibata, and Daisuke Sekine. "Synthetic Studies on Keramaphidin B: Formation of a Macrocyclic Ring by Intramolecular Diels-Alder Reaction." HETEROCYCLES 100, no. 1 (2020): 3. http://dx.doi.org/10.3987/com-19-14117.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Alekseeva, Kseniia A., Elizaveta A. Kvyatkovskaya, Eugeniya V. Nikitina, et al. "Transposition of Aromaticity from a Furan to a Cyclohexane Ring in Furoisoindoles During the Interaction of 3-(Furyl)allylamines with Bromomaleic Anhydride." Synlett 31, no. 03 (2020): 255–60. http://dx.doi.org/10.1055/s-0039-1690782.

Full text

Abstract:

An unexpected four-step reaction sequence was discovered in the course of investigation of the interaction between 3-(furan-2-yl)allylamines and bromomaleic anhydride. This conversion begins with the initial N-acylation of the allylamines by the anhydride, followed by intramolecular Diels–Alder reaction, which is accompanied by a dehydrohalogenation, and ends with the formation of partially unsaturated furo[2,3-f]isoindoles followed by transposition of aromaticity from the furan moiety to the neighboring cyclohexane ring. The reaction between 3-(furan-3-yl)allylamines and bromomaleic anhydride

APA, Harvard, Vancouver, ISO, and other styles

11

Obushak, Mykola D., Fedor I. Zubkov, Maryana A. Nadirova та ін. "Application of the Intramolecular Diels–Alder Vinylarenе (IMDAV) Approach for the Synthesis of Thieno[2,3-f]isoindoles". Synthesis 52, № 15 (2020): 2196–223. http://dx.doi.org/10.1055/s-0039-1690833.

Full text

Abstract:

3-(Thien-2-yl)- and 3-(thien-3-yl)allylamines, readily accessible from the corresponding thienyl aldehydes, can interact with a broad range of anhydrides and α,β-unsaturated acids chlorides (maleic, сitraconic, and phenyl maleic anhydrides, сrotonyl and сinnamyl chlorides, etc.) leading to the formation of a thieno[2,3-f]isoindole core. Usually, the reaction sequence involves three successive steps: acylation of the nitrogen atom of the initial allylamine, the intramolecular Diels–Alder vinylarenе (IMDAV) reaction, and the final aromatization of the dihydrothiophene ring in the Diels–Alder ad

APA, Harvard, Vancouver, ISO, and other styles

12

Khasiyatullina, Nadezhda R., Tamara A. Baronova, Ekaterina V. Mironova, et al. "Tandem dihetero-Diels–Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes." Organic Chemistry Frontiers 5, no. 21 (2018): 3113–28. http://dx.doi.org/10.1039/c8qo00915e.

Full text

APA, Harvard, Vancouver, ISO, and other styles

13

Ndibwami, Alexis, Serge Lamothe, Pierre Soucy, Solo Goldstein, and Pierre Deslongchamps. "Transannular Diels–Alder reactions on 14-membered macrocyclic trienes. Part II: formation of macrocycles and thermal conversion into tricyclic systems." Canadian Journal of Chemistry 71, no. 5 (1993): 714–25. http://dx.doi.org/10.1139/v93-095.

Full text

Abstract:

In the preceding paper (Part I) we described the synthesis of eight isomeric acyclic trienes. These compounds could be transformed into the corresponding macrocyclic trienes, which were further converted into tricyclic A.B.C.[6.6.6] products by a thermal transannular Diels–Alder reaction. The experimental results of this study and their analysis are reported in the present paper. The comparison with theoretical predictions is also discussed.

APA, Harvard, Vancouver, ISO, and other styles

14

Kotha, Sambasivarao, Subba Cheekatla, and Darshan Mhatre. "Ring-Closing Metathesis Approach to Cage Propellanes Containing Oxepane and Tetrahydrofuran Hybrid System." Synthesis 49, no. 24 (2017): 5339–50. http://dx.doi.org/10.1055/s-0036-1591726.

Full text

Abstract:

The preparation of a variety of structurally interesting oxygenated cage compounds involving atom-economic processes such as Claisen rearrangement, Diels–Alder reaction, [2+2] photocycloaddition, and ring-closing metathesis (RCM) as key steps is reported. For the first time, oxepane ring system is introduced in cage framework using olefin metathesis as a key step. These cage systems assembled here are difficult to prepare by traditional methods. The synthetic sequence described here opens up new routes to higher order polycycles containing heteroatoms without the involvement of protecting grou

APA, Harvard, Vancouver, ISO, and other styles

15

Hofmann, Hans, Gerhard Löw, and Armin Haag. "Heterocyclische Siebenring-Verbindungen, XXIX [1] Bildung und Abfangreaktionen von substituierten 2,3-Dehydro- 1,5-benzodioxepinen / Heterocyclic Seven-Membered Ring Compounds, XXIX [1] Formation and Trapping Reactions of Substituted 2,3-Dehydro-1,5-benzodioxepins." Zeitschrift für Naturforschung B 40, no. 11 (1985): 1575–79. http://dx.doi.org/10.1515/znb-1985-1128.

Full text

Abstract:

4-Cyano- and 4-Carbomethoxy-3,4-dihydro-2H-l,5-benzodioxepin-3-one (1a and 1b) have been converted to the corresponding enol-toluenesulfonates 2a and 2b, respectively. Reaction of 2a and 2b with base led to the heterocyclic allenes 3a resp. 3b, which could be trapped by Diels-Alder-reaction with furane, yielding the cycloadducts 4a and 4b.

APA, Harvard, Vancouver, ISO, and other styles

16

Hall, Dennis G., Renate Müller, and Pierre Deslongchamps. "Studies on the transannular Diels–Alder reaction of 15-membered macrocyclic trienes containing a trans-trans diene. Part II: Evidence for unsymmetrical transition states in the formation of A.B.C.[6.6.7] tricyclic products." Canadian Journal of Chemistry 73, no. 10 (1995): 1695–710. http://dx.doi.org/10.1139/v95-208.

Full text

Abstract:

In the preceding paper (Part I) we described the preparation of 10 model TTT and TTC cyclopentadecatrienes. Their conversion to A.B.C.[6.6.7] tricyclic products via a transannular Diels–Alder (TADA) reaction and the analysis of the resulting diastereoselection along with proofs of structures are described in the present article (Part II). The required temperature of reaction was significantly higher (~100 °C) in comparison to that required for the 14-membered lower homologs, indicating that proximity effects are playing a key role in the TADA reaction. The presence of ester groups in the chain

APA, Harvard, Vancouver, ISO, and other styles

17

Heravi, Majid M., Mahzad Dehghani, Vahideh Zadsirjan, and Manijheh Ghanbarian. "Alkynes as Privileged Synthons in Selected Organic Name Reactions." Current Organic Synthesis 16, no. 2 (2019): 205–43. http://dx.doi.org/10.2174/1570179416666190126100744.

Full text

Abstract:

Background:Alkynes are actually basic chemicals, serving as privileged synthons for planning new organic reactions for assemblage of a reactive motif, which easily undergoes a further desirable transformation. Name reactions, in organic chemistry are referred to those reactions which are well-recognized and reached to such status for being called as their explorers, discoverers or developers. Alkynes have been used in various name reactions. In this review, we try to underscore the applications of alkynes as privileged synthons in prevalent name reactions such as Huisgen 1,3-dipolar cycloaddti

APA, Harvard, Vancouver, ISO, and other styles

18

Samy, Mamdouh N., Géraldine Le Goff, Philippe Lopes, et al. "Osmanicin, a Polyketide Alkaloid Isolated from Streptomyces osmaniensis CA-244599 Inhibits Elastase in Human Fibroblasts." Molecules 24, no. 12 (2019): 2239. http://dx.doi.org/10.3390/molecules24122239.

Full text

Abstract:

The strain Streptomyces osmaniensis CA-244599 isolated from the Comoros islands was submitted to liquid-state fermentation coupled to in situ solid-phase extraction with amberlite XAD-16 resin. Elution of the trapped compounds on the resin beads by ethyl acetate afforded seven metabolites, osmanicin (1), streptazolin (2), streptazone C (3), streptazone B1 (4), streptenol C (5), nocardamine (6) and desmethylenylnocardamine (7). Osmanicin (1) is a newly reported unusual scaffold combining streptazolin (2) and streptazone C (3) through a Diels-Alder type reaction. Experimental evidence excluded t

APA, Harvard, Vancouver, ISO, and other styles

19

Vida, Norbert, Jiří Václavík, and Petr Beier. "Synthesis and reactivity of aliphatic sulfur pentafluorides from substituted (pentafluorosulfanyl)benzenes." Beilstein Journal of Organic Chemistry 12 (January 20, 2016): 110–16. http://dx.doi.org/10.3762/bjoc.12.12.

Full text

Abstract:

Oxidation of 3- and 4-pentafluorosulfanyl-substituted anisoles and phenols with hydrogen peroxide and sulfuric acid provided a mixture of SF5-substituted muconolactone, maleic, and succinic acids. A plausible mechanism for the formation of the aliphatic SF5 compounds was presented and their chemical reactivity was investigated. SF5-substituted para-benzoquinone was synthesized; its oxidation led to an improved yield of 2-(pentafluorosulfanyl)maleic acid. The reaction of SF5-substituted maleic anhydride and para-benzoquinone with cyclopentadiene afforded the Diels–Alder adducts. Decomposition o

APA, Harvard, Vancouver, ISO, and other styles

20

Bakhtiari, Atefeh, and Javad Safaei-Ghomi. "Effects of Chiral Ligands on the Asymmetric Carbonyl-Ene Reaction." Synlett 30, no. 15 (2019): 1738–64. http://dx.doi.org/10.1055/s-0037-1611875.

Full text

Abstract:

The carbonyl-ene reaction is one of the most well-known reactions for C–C bond formation. Based on frontier molecular orbitals (FMO), carbonyl-ene reactions occur between the highest occupied molecular orbital (HOMO) of the ene compound bearing an active hydrogen atom at the allylic center and the lowest unoccupied molecular orbital (LUMO) of the electron-deficient enophile, which is a carbonyl compound. A high activation barrier enforces the concerted ene reaction rather than a Diels–Alder reaction at high temperature. Employing a catalytic system can eliminate defects in the ene reaction, an

APA, Harvard, Vancouver, ISO, and other styles

21

El Kharrat, Salem, Philippe Laurent, Laurent Boiteau, and Hubert Blancou. "Novel Synthesis of Substituted 2-Trifluoromethyl and 2-Perfluoroalkyl N-Arylpyridinium Compounds—Mechanistic Insights." Molecules 24, no. 12 (2019): 2328. http://dx.doi.org/10.3390/molecules24122328.

Full text

Abstract:

We report a new one-pot synthesis of 2-trifluoromethylated/2-perfluoroalkylated N-aryl-substituted pyridiniums, 5,6,7,8-tetrahydroquinoliniums and 6,7,8,9-tetrahydro-5H-cyclohepta[b]-pyridinium compounds starting from an activated β-dicarbonyl analogue (here a perfluoro-alkylated gem-iodoacetoxy derivative), an aromatic amine and a (cyclic or acyclic) ketone. The key step of this multicomponent reaction, involves the formation of a 3-perfluoroalkyl-N,N’-diaryl-1,5-diazapentadiene intermediate, various examples of which were isolated and characterized for the first time, together with investiga

APA, Harvard, Vancouver, ISO, and other styles

22

Kolaříková, Viola, Markéta Rybáčková, Martin Svoboda, and Jaroslav Kvíčala. "Ring-closing metathesis of prochiral oxaenediynes to racemic 4-alkenyl-2-alkynyl-3,6-dihydro-2H-pyrans." Beilstein Journal of Organic Chemistry 16 (November 13, 2020): 2757–68. http://dx.doi.org/10.3762/bjoc.16.226.

Full text

Abstract:

The prochiral 4-(allyloxy)hepta-1,6-diynes, optionally modified in the positions 1 and 7 with an alkyl or ester group, undergo a chemoselective ring-closing enyne metathesis yielding racemic 4-alkenyl-2-alkynyl-3,6-dihydro-2H-pyrans. Among the catalysts tested, Grubbs 1st generation precatalyst in the presence of ethene (Mori conditions) gave superior results compared to the more stable Grubbs or Hoveyda–Grubbs 2nd generation precatalysts. This is probably caused by a suppression of the subsequent side-reactions of the enyne metathesis product with ethene. On the other hand, the 2nd generation

APA, Harvard, Vancouver, ISO, and other styles

23

Jursic, Branko S. "Computational investigation of the suitability of heterocyclic aromatic compounds with two heteroatoms in the 1 and 3 ring positions as dienes for the diels alder reaction." Journal of Heterocyclic Chemistry 35, no. 6 (1998): 1467–71. http://dx.doi.org/10.1002/jhet.5570350642.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

Masdeu, Carme, Maria Fuertes, Endika Martin-Encinas, et al. "Fused 1,5-Naphthyridines: Synthetic Tools and Applications." Molecules 25, no. 15 (2020): 3508. http://dx.doi.org/10.3390/molecules25153508.

Full text

Abstract:

Heterocyclic nitrogen compounds, including fused 1,5-naphthyridines, have versatile applications in the fields of synthetic organic chemistry and play an important role in the field of medicinal chemistry, as many of them have a wide range of biological activities. In this review, a wide range of synthetic protocols for the construction of this scaffold are presented. For example, Friedländer, Skraup, Semmlere-Wolff, and hetero-Diels-Alder, among others, are well known classical synthetic protocols used for the construction of the main 1,5-naphthyridine scaffold. These syntheses are classified

APA, Harvard, Vancouver, ISO, and other styles

25

Domingo, Luis R., and Juan Andrés. "Enhancing Reactivity of Carbonyl Compounds via Hydrogen-Bond Formation. A DFT Study of the Hetero-Diels−Alder Reaction between Butadiene Derivative and Acetone in Chloroform." Journal of Organic Chemistry 68, no. 22 (2003): 8662–68. http://dx.doi.org/10.1021/jo030156s.

Full text

APA, Harvard, Vancouver, ISO, and other styles

26

Mlostoń, Grzegorz, Katarzyna Urbaniak, Malwina Sobiecka, et al. "Hetero-Diels-Alder Reactions of In Situ-Generated Azoalkenes with Thioketones; Experimental and Theoretical Studies." Molecules 26, no. 9 (2021): 2544. http://dx.doi.org/10.3390/molecules26092544.

Full text

Abstract:

The hetero-Diels-Alder reactions of in situ-generated azoalkenes with thioketones were shown to offer a straightforward method for an efficient and regioselective synthesis of scarcely known N-substituted 1,3,4-thiadiazine derivatives. The scope of the method was fairly broad, allowing the use of a series of aryl-, ferrocenyl-, and alkyl-substituted thioketones. However, in the case of N-tosyl-substituted cycloadducts derived from 1-thioxo-2,2,4,4-tetramethylcyclobutan-3-one and the structurally analogous 1,3-dithione, a more complicated pathway was observed. By elimination of toluene sulfinic

APA, Harvard, Vancouver, ISO, and other styles

27

Nair, Mangalam, Beena James, and E. Suresh. "Hetero-Diels-Alder Reaction of 3-Bromo-7-(bromomethyl)tetracyclo[5.3.1.02,6.04,8]undec-10(12)-ene-9,11-dione with Pentafulvenes: Facile Synthesis of Novel Polycyclic Cage Compounds Having a Pyran Ring." Synlett 2006, no. 20 (2006): 3479–83. http://dx.doi.org/10.1055/s-2006-956481.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

Dembitsky, V. M., G. A. Tolstikov та M. Srebnik. "Boranes in Organic Chemistry 2. β-Aminoalkyl- and β-sulfanylalkylboranes in organic synthesis". Eurasian Chemico-Technological Journal 4, № 3 (2017): 153. http://dx.doi.org/10.18321/ectj528.

Full text

Abstract:

<p>Problems on using of β-aminoalkyl- and β-sulfanylalkylboranes in organic synthesis are considered in this review. The synthesis of boron containing a-aminoacids by Curtius rearrangement draws attention. The use of β-aminoalkylboranes available by enamine hydroboration are described. Examples of enamine desamination with the formation of alkenes, aminoalcohols and their transformations into allylic alcohol are presented. These conversions have been carried out on steroids and nitrogen containing heterocyclic compounds. The dihydroboration of N-vinyl-carbamate and N-vinyl-urea have been

APA, Harvard, Vancouver, ISO, and other styles

29

Serra, Massimo, Eric Bernardi, and Lino Colombo. "Recent Advances in One-Pot Enyne Metathesis Processes for the Preparation of Biologically and Medicinally Relevant Compounds." Synthesis, November 9, 2020. http://dx.doi.org/10.1055/s-0040-1705965.

Full text

Abstract:

AbstractEnyne metathesis reactions are powerful tools for the preparation of a wide range of synthetic and natural chemical substances with increasing efficiency and environmental sustainability. The driving force of the reaction is the formation of a stable conjugated system, i.e., a diene, which through further functionalization steps can be used for the construction of skeletally complex molecular architectures. These concepts are exploited to design cascade reaction sequences, where multiple rings can be formed in a one-pot fashion by combining metathetic protocols with various chemical tr

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!