(S)- or (R)-3-(E-Enoyl)-4-phenyl-1,3- oxazolidin-2-ones: Ideal Michael Acceptors To Afford a Virtually Complete Control of Simple and Face Diastereoselectivity in Addition Reactions with Glycine Derivatives
Тип публикации: Journal Article
Дата публикации: 2000-02-24
SCImago Q1
Tоп 10% SCImago
WOS Q1
БС1
SJR: 1.007
CiteScore: 8.7
Impact factor: 5
ISSN: 15237060, 15237052
PubMed ID:
10754676
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Краткое описание
[formula: see text] Enantiomerically pure (S)- or (R)-3-(E-enoyl)-4-phenyl-1,3-oxazolidin-2-ones were found to serve as ideal Michael acceptors in addition reactions with achiral Ni(II) complexes of glycine Schiff bases. Virtually complete control of simple and face diastereoselectivity, observed in these reactions, combined with quantitative chemical yields renders this methodology synthetically superior to the previous methods.
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Soloshonok V. A., Cai C., Hruby V. J. (S)- or (R)-3-(E-Enoyl)-4-phenyl-1,3- oxazolidin-2-ones: Ideal Michael Acceptors To Afford a Virtually Complete Control of Simple and Face Diastereoselectivity in Addition Reactions with Glycine Derivatives // Organic Letters. 2000. Vol. 2. No. 6. pp. 747-750.
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Soloshonok V. A., Cai C., Hruby V. J. (S)- or (R)-3-(E-Enoyl)-4-phenyl-1,3- oxazolidin-2-ones: Ideal Michael Acceptors To Afford a Virtually Complete Control of Simple and Face Diastereoselectivity in Addition Reactions with Glycine Derivatives // Organic Letters. 2000. Vol. 2. No. 6. pp. 747-750.
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TY - JOUR
DO - 10.1021/ol990402f
UR - https://pubs.acs.org/doi/10.1021/ol990402f
TI - (S)- or (R)-3-(E-Enoyl)-4-phenyl-1,3- oxazolidin-2-ones: Ideal Michael Acceptors To Afford a Virtually Complete Control of Simple and Face Diastereoselectivity in Addition Reactions with Glycine Derivatives
T2 - Organic Letters
AU - Soloshonok, Vadim A.
AU - Cai, Chaozhong
AU - Hruby, Victor J.
PY - 2000
DA - 2000/02/24
PB - American Chemical Society (ACS)
SP - 747-750
IS - 6
VL - 2
PMID - 10754676
SN - 1523-7060
SN - 1523-7052
ER -
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BibTex (до 50 авторов)
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@article{2000_Soloshonok,
author = {Vadim A. Soloshonok and Chaozhong Cai and Victor J. Hruby},
title = {(S)- or (R)-3-(E-Enoyl)-4-phenyl-1,3- oxazolidin-2-ones: Ideal Michael Acceptors To Afford a Virtually Complete Control of Simple and Face Diastereoselectivity in Addition Reactions with Glycine Derivatives},
journal = {Organic Letters},
year = {2000},
volume = {2},
publisher = {American Chemical Society (ACS)},
month = {feb},
url = {https://pubs.acs.org/doi/10.1021/ol990402f},
number = {6},
pages = {747--750},
doi = {10.1021/ol990402f}
}
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MLA
Скопировать
Soloshonok, Vadim A., et al. “(S)- or (R)-3-(E-Enoyl)-4-phenyl-1,3- oxazolidin-2-ones: Ideal Michael Acceptors To Afford a Virtually Complete Control of Simple and Face Diastereoselectivity in Addition Reactions with Glycine Derivatives.” Organic Letters, vol. 2, no. 6, Feb. 2000, pp. 747-750. https://pubs.acs.org/doi/10.1021/ol990402f.
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