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Journal articles on the topic 'N-(β'

Author: Grafiati

Published: 4 June 2021

Last updated: 18 February 2022

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1

Monteiro, Luís S., Juliana J. Andrade та Ana C. Suárez. "Synthesis of New N-Ethyl Dehydroamino Acid Derivatives: N-Ethyl β,β-Dibromo, N-Ethyl β-Bromo β-Substituted, and N-Ethyl β,β-Disubstituted N-Protected Dehydroamino Acid Methyl Esters". European Journal of Organic Chemistry 2011, № 33 (2011): 6764–72. http://dx.doi.org/10.1002/ejoc.201100907.

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2

Gailius, Viktoras, та Helmut Stamm. "N-(β-Cyanethyl)-N-nitrosoharnstoffe". Archiv der Pharmazie 326, № 6 (1993): 373. http://dx.doi.org/10.1002/ardp.19933260612.

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3

LUK'YANOV, O. A., G. A. SMIRNOV та V. V. SEVOST'YANOVA. "ChemInform Abstract: β,β-Dinitro Derivatives of N-Alkyl-N′-alkoxydiazene N-Oxides." ChemInform 26, № 50 (2010): no. http://dx.doi.org/10.1002/chin.199550053.

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4

Kraska, J., та J. Sokołowska-Gajda. "Synthesis and properties of some alkyl esters of N-benzyl-N-phenyl-β-alanine and N-(β-phenylethyl)-N-phenyl-β-alanine". Dyes and Pigments 7, № 3 (1986): 161–69. http://dx.doi.org/10.1016/0143-7208(86)85007-0.

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5

Urpí, Lourdes, Katia Jiménez, Xavier Solans, Alfonso Rodríguez-Galán та Jordi Puiggalí. "N-Chloroacetyl-β-alanine". Acta Crystallographica Section C Crystal Structure Communications 59, № 1 (2002): o24—o26. http://dx.doi.org/10.1107/s0108270102020814.

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6

Shan, Shang, Yan-Ling Zhang та Duan-Jun Xu. "Methyl β-N-phenylmethylenedithiocarbazate". Acta Crystallographica Section E Structure Reports Online 62, № 4 (2006): o1567—o1569. http://dx.doi.org/10.1107/s1600536806010300.

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Crystals of the title compound, C9H10N2S2, were obtained from a condensation reaction of methyl dithiocarbazate and benzaldehyde. The planar dithiocarbazate unit is tilted with respect to the phenyl plane with a dihedral angle of 10.96 (12)°. Intermolecular N—H...S hydrogen bonding stabilizes the crystal structure. A C—H...π interaction is also observed in the crystal structure.

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7

Peters, Arnold T., та Adam Gbadamosi. "Disperse dyes: 4-hetarylazo derivatives from N-β-cyanoethyl-N-β-hydroxyethylaniline". Journal of Chemical Technology & Biotechnology 53, № 3 (2007): 301–8. http://dx.doi.org/10.1002/jctb.280530312.

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8

Georgiadou, Kyriaki L., та Eforia G. Tsatsaroni. "Hetarylazo disperse dyes derived from substituted N,N-bis-β-hydroxy- and N,N-bis-β-acetoxy-ethylaniline". Dyes and Pigments 53, № 1 (2002): 73–78. http://dx.doi.org/10.1016/s0143-7208(02)00005-0.

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9

Bulychev, Alexey, John R. Bellettini, Michael O'Brien та ін. "N-Sulfonyloxy-β-lactam Inhibitors for β-Lactamases". Tetrahedron 56, № 31 (2000): 5719–28. http://dx.doi.org/10.1016/s0040-4020(00)00427-0.

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10

Tanizawa, Kazutaka, Keiko Santoh та Yuichi Kanaoka. "N -Nitroso-β-lactams as β-lactamase inhibitor". FEBS Letters 250, № 2 (1989): 218–20. http://dx.doi.org/10.1016/0014-5793(89)80724-0.

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11

Bennani, Youssef L., та K. Barry Sharpless. "Asymmetric dihydroxylation (AD) of N,N-dialkyl and N-methoxy-N-methyl α,β- and β,γ-unsaturated amides". Tetrahedron Letters 34, № 13 (1993): 2079–82. http://dx.doi.org/10.1016/s0040-4039(00)60350-7.

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12

Makarov, V. A., та V. G. Granik. "ChemInform Abstract: Synthesis and Properties of β,β-Bisfunctionalized Ketene N,N-Acetals". ChemInform 30, № 17 (2010): no. http://dx.doi.org/10.1002/chin.199917329.

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13

Alotaibi, A. M., M. A. El-Moneam та M. S. M. Noorani. "On the rational difference equation y n + 1 = α 0 y n + α 1 y n − p + α 2 y n − q + α 3 y n − r + α 4 y n − s β 0 y n + β 1 y n − p + β 2 y n − q + β 3 y n − r + β 4 y n − s". Journal of Nonlinear Sciences and Applications 11, № 01 (2017): 80–97. http://dx.doi.org/10.22436/jnsa.011.01.07.

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14

Cabezas, J. A. "Some comments on the type references of the official nomenclature (IUB) for β-N-acetylglucosaminidase, β-N-acetylhexosaminidase and β-N-acetylgalactosaminidase". Biochemical Journal 261, № 3 (1989): 1059–60. http://dx.doi.org/10.1042/bj2611059b.

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15

Fleming, Ian, Elena Marangon, Chiara Roni, Matthew G. Russell та Sandra Taliansky Chamudis. "Reactions of phenyldimethylsilyllithium with β-N,N-dimethylaminoenones". Chemical Communications, № 2 (17 грудня 2002): 200–201. http://dx.doi.org/10.1039/b210444j.

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16

Parvez, M., S. Ali, M. H. Bhatti, M. N. Khokhar, M. Mazhar та S. I. Qureshi. "Tri-n-butyl(N-maleoyl-β-alaninato)tin". Acta Crystallographica Section C Crystal Structure Communications 55, № 9 (1999): 1427–29. http://dx.doi.org/10.1107/s010827019900743x.

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17

GAILIUS, V., та H. STAMM. "ChemInform Abstract: N-(β-Cyanoethyl)-N-nitroso Ureas." ChemInform 24, № 47 (2010): no. http://dx.doi.org/10.1002/chin.199347164.

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18

Montgomery, Craig T., Alan J. Freyer, Hélène Guinaudeau та ін. "(+)-N-Methyllaurotetanine-β-N-Oxide from Glossocalyx brevipes". Journal of Natural Products 48, № 5 (1985): 833–34. http://dx.doi.org/10.1021/np50041a025.

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19

Gridchin, S. N. "Protolytic equilibria of N-(β-hydroxyethyl)ethylenediamine-N,N′,N′-triacetic acid". Russian Journal of Inorganic Chemistry 53, № 10 (2008): 1672–76. http://dx.doi.org/10.1134/s0036023608100252.

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20

IQBAL, M. Perwaiz, Khawar KAZMI та Naseema MEHBOOBALI. "N-acetyl-β-D-glucosaminidase". Acta Cardiologica 60, № 5 (2005): 509–13. http://dx.doi.org/10.2143/ac.60.5.2004972.

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21

Ferreira, P. M., I. Jack та D. R. T. Jones. "Large-N supersymmetric β-functions". Physics Letters B 399, № 3-4 (1997): 258–62. http://dx.doi.org/10.1016/s0370-2693(97)00291-8.

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22

Gers-Barlag, H., I. Bartz та H. Rüdiger. "β-N-Acetylhexosaminidase from soybean". Phytochemistry 27, № 12 (1988): 3739–41. http://dx.doi.org/10.1016/0031-9422(88)83009-7.

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23

Bertolotto, Corine. "β-caténine et N-ras". médecine/sciences 24, № 2 (2008): 122–23. http://dx.doi.org/10.1051/medsci/2008242122.

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24

Nehls, Irene, Olaf Hanebeck, Roland Becker та Franziska Emmerling. "N-(β-Carboxyethyl)-α-isoleucine". Acta Crystallographica Section E Structure Reports Online 69, № 2 (2013): o172—o173. http://dx.doi.org/10.1107/s160053681205146x.

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The title compound, {2-[(2-carbamoylethyl)amino]-3-methylpentanoic acid}, C9H18N2O3, is of interest with respect to its biological activity. It was formed during an addition reaction between acrylamide and the amino acid isoleucine. The crystal structure is a three-dimensional network built up by intermolecular N—H...O and O—H...N hydrogen bonds.

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25

Downey, James M., та Michael V. Cohen. "O -Linked β- N -Acetylglucosamine". Circulation Research 104, № 1 (2009): 7–8. http://dx.doi.org/10.1161/circresaha.108.191163.

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26

Perry, Thomas L., Catherine Bergeron, Andrew J. Biro та Shirley Hansen. "β-N-Methylamino-l-alanine". Journal of the Neurological Sciences 94, № 1-3 (1989): 173–80. http://dx.doi.org/10.1016/0022-510x(89)90227-x.

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27

TOUJAS, J. L., E. JOST та M. VAULTIER. "ChemInform Abstract: Synthesis of Homochiral N-Boc-β-Aminoaldehydes from N-Boc-β-aminonitriles." ChemInform 29, № 51 (2010): no. http://dx.doi.org/10.1002/chin.199851229.

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28

Uhlig, Egon, та Bernd Machelett. "Über die Komplexbildungstendenz des N-(β-Diphenylphosphinoäthyl)-salicylaldimins und des N-(β-Diphenylarsinoäthyl)-salicylaldimins". Zeitschrift für Chemie 9, № 7 (2010): 274–75. http://dx.doi.org/10.1002/zfch.19690090713.

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29

Shiau, Timothy P., Ashley Houchin, Satheesh Nair та ін. "Stieglitz rearrangement of N,N-dichloro-β,β-disubstituted taurines under mild aqueous conditions". Bioorganic & Medicinal Chemistry Letters 19, № 4 (2009): 1110–14. http://dx.doi.org/10.1016/j.bmcl.2008.12.109.

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30

Kunugi, Akira, Mikito Yasuzawa та Hiroshi Matsui. "Electrochemical carboxylation of β-methylsulphenyl-β-methylsulphonylstyrene in N,N,-dimethylformamide containing carbon dioxide". Electrochimica Acta 36, № 8 (1991): 1341–44. http://dx.doi.org/10.1016/0013-4686(91)80014-y.

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31

Van Langevelde, Arjen, Kees Van Malssen, René Driessen та ін. "Structure of C n C n+2C n -type (n = even) β′-triacylglycerols". Acta Crystallographica Section B Structural Science 56, № 6 (2000): 1103–11. http://dx.doi.org/10.1107/s0108768100009927.

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The crystal structures of the β′ phase of CLC (1,3-didecanoyl-2-dodecanoylglycerol) and MPM (1,3-ditetradecanoyl-2-hexadecanoylglycerol) have been determined from single-crystal X-ray diffraction and high-resolution X-ray powder diffraction data, respectively. Both these crystals are orthorhombic with space group Iba2 and Z = 8. The unit-cell parameters of β′-CLC are a = 57.368 (6), b = 22.783 (2) and c = 5.6945 (6) Å and the final R value is 0.175. The unit-cell parameters of β′-MPM are a = 76.21 (4), b = 22.63 (1) and c = 5.673 (2) Å and the final Rp value is 0.057. Both the β′-CLC and β′-MP

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32

Teng, Min, Marvin J. Miller, Thalia I. Nicas, Jana Grissom-Arnold та Robin D. G. Cooper. "β-Lactamase inhibitors derived from N-tosyloxy-β-lactams". Bioorganic & Medicinal Chemistry 1, № 2 (1993): 151–54. http://dx.doi.org/10.1016/s0968-0896(00)82113-6.

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33

BENNANI, Y. L., та K. B. SHARPLESS. "ChemInform Abstract: Asymmetric Dihydroxylation (AD) of N,N-Dialkyl and N-Methoxy-N-methyl . alpha.,β- and β,γ-Unsaturated Amides." ChemInform 24, № 34 (2010): no. http://dx.doi.org/10.1002/chin.199334051.

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34

Oikonomakos, Nikos G., Magda Kosmopoulou, Spyros E. Zographos та ін. "Binding of N -acetyl-N ′-β-d -glucopyranosyl urea and N -benzoyl-N ′-β-d -glucopyranosyl urea to glycogen phosphorylase b". European Journal of Biochemistry 269, № 6 (2002): 1684–96. http://dx.doi.org/10.1046/j.1432-1327.2002.02813.x.

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35

Hojo, Masaru, Ryōichi Masuda, Etsuji Okada, Hiromi Yamamoto, Katsushi Morimoto та Ken Okada. "Facile Synthesis of β-TrifluoroacetylketeneO,N-,S,N- andN,N-Acetals". Synthesis 1990, № 03 (1990): 195–98. http://dx.doi.org/10.1055/s-1990-26827.

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36

Smelka, Leszek, Barbara Rzeszotarska, Malgorzata A. Broda та Zbigniew Kubica. "N-ACETYL-α,β-DEHYDROAMINO ACIDN'-METHYLAMIDES AND N',N'-DIMETHYLAMIDES". Organic Preparations and Procedures International 29, № 6 (1997): 696–701. http://dx.doi.org/10.1080/00304949709355251.

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37

Leblond, Jeffrey D., Aaron S. Dahmen, Vernon J. Dodson та Jeremy L. Dahmen. "Characterization of the Betaine Lipids, Diacylglyceryl-N,N,N-trimethylhomoserine (DGTS) and Diaclyglycerylhydroxymethyl-N,N,N-trimethyl-β-alanine (DGTA), in Brown- and Green-Pigmented Raphidophytes". Algological Studies 142 (1 травня 2013): 17–27. http://dx.doi.org/10.1127/1864-1318/2013/0130.

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38

Cunico, Robert F., та Chia P. Kuan. "Oxazoles from β-acyloxy-n,n-bis(trimethylsilyl)enamines". Tetrahedron Letters 31, № 14 (1990): 1945–48. http://dx.doi.org/10.1016/s0040-4039(00)88885-1.

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39

Yanagawa, T., та H. Kanbara. "Photodarkening in 4-(N,N-diethylamino)-β-nitrostyrene solutions". Applied Physics Letters 71, № 2 (1997): 187–89. http://dx.doi.org/10.1063/1.119496.

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40

Shul'gina, N. B., L. V. Grigorenko, M. V. Zhukov та J. M. Bang. "8He β-decay to the 6Li+n+n channel". Nuclear Physics A 619, № 1-2 (1997): 143–50. http://dx.doi.org/10.1016/s0375-9474(97)00151-6.

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41

Andruszkiewicz, Ryszard, та Andrzej Czerwiński. "Dehydration of β-Hydroxyamino Acids with N,N′-Carbonyldiimidazole". Synthesis 1982, № 11 (2002): 968–69. http://dx.doi.org/10.1055/s-1982-30026.

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42

Bull, Steven D., Stephen G. Davies, Peter M. Kelly, Massimo Gianotti та Andrew D. Smith. "Orthogonal N,N-deprotection strategies of β-amino esters". Journal of the Chemical Society, Perkin Transactions 1, № 23 (12 листопада 2001): 3106–11. http://dx.doi.org/10.1039/b106389h.

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43

Zarei, Maaroof, та Aliasghar Jarrahpour. "Synthesis of N-unsubstituted β-lactams from N-alkoxyphenyl-β-lactams with cobalt(III) fluoride". Tetrahedron Letters 51, № 44 (2010): 5791–94. http://dx.doi.org/10.1016/j.tetlet.2010.08.101.

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44

Chen, Xiaodi, Lan Jin, Xukai Jiang та ін. "Converting a β-N-acetylhexosaminidase into two trans-β-N-acetylhexosaminidases by domain-targeted mutagenesis". Applied Microbiology and Biotechnology 104, № 2 (2019): 661–73. http://dx.doi.org/10.1007/s00253-019-10253-y.

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45

Gafurov, M. B., D. N. Dalimov, F. G. Kamaev, G. M. Vaizburg та A. A. Abduvakhabov. "Synthesis, structure, and anticholinesterase activities of methylphosphonothionates of N-β-hydroxyethylmorpholine and N-β-hydroxypropylmorpholine". Chemistry of Natural Compounds 25, № 4 (1989): 465–68. http://dx.doi.org/10.1007/bf00597659.

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46

Bruneau, Christian, Jean-Luc Renaud, Hania Hebbache та Zakia Hank. "Hydrogenation of β-N-Substituted and β-N,N-Disubstituted Enamino Esters in the Presence of Iridium(I) Catalyst". Synthesis 2009, № 15 (2009): 2627–33. http://dx.doi.org/10.1055/s-0029-1217405.

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47

Weignerová, Lenka, Petra Vavrušková, Andrea Pišvejcová, Joachim Thiem та Vladimı́r Křen. "Fungal β-N-acetylhexosaminidases with high β-N-acetylgalactosaminidase activity and their use for synthesis of β-GalNAc-containing oligosaccharides". Carbohydrate Research 338, № 9 (2003): 1003–8. http://dx.doi.org/10.1016/s0008-6215(03)00044-2.

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48

Uneyama, Kenji, та Tsuyoshi Kato. "N-TMS-β,β-difluoroenamines: Electrochemical preparation and its transformation". Tetrahedron Letters 39, № 7 (1998): 587–90. http://dx.doi.org/10.1016/s0040-4039(97)10613-x.

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49

Makarov, Vadim A., та Vladimir G. Granik. "Synthesis and properties of β,β-bisfunctionalised keteneN,N-acetals". Russian Chemical Reviews 67, № 11 (1998): 923–40. http://dx.doi.org/10.1070/rc1998v067n11abeh000422.

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50

Dettwiler, James E., та William D. Lubell. "Diversity-oriented synthesis of enantiopure N-protected β,β-dialkylserines". Canadian Journal of Chemistry 82, № 2 (2004): 318–24. http://dx.doi.org/10.1139/v03-193.

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A series of enantiomerically pure N-Boc-protected β,β-dialkylserines was synthesized by addition of the appropriate Grignard reagent to N-(Boc)serine methyl ester, followed by TEMPO-catalysed oxidation of the primary alcohol with sodium chlorite and sodium hypochlorite.Key words: amino acid, serine, β,β-dialkylserines, ring-closing metathesis.

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