том 25 издание 19 страницы 2895-2900

Catalytic Hydrogenation of Chiral 2-(2-Furyl)-3,4-dimethyl-5-phenyloxazolidine

Тип публикацииJournal Article
Дата публикации1995-10-01
scimago Q3
wos Q3
БС2
SJR0.322
CiteScore4.3
Impact factor1.8
ISSN00397911, 15322432
Organic Chemistry
Краткое описание
Reduction of chiral 2-(2-furyl)-3,4-dimethyl-5-phenyloxazo-lidines-1,3 by H2/Raney nickel proceeds simultaneously as hydrogenation of the furan ring and opening of the oxazolidine ring on C2-O bond. Diastere-oselectivity in the first reaction was established as ca 40% and 80% depending on the configuration of the oxazolidine 1 and 2.
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ГОСТ |
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Polyak F. et al. Catalytic Hydrogenation of Chiral 2-(2-Furyl)-3,4-dimethyl-5-phenyloxazolidine // Synthetic Communications. 1995. Vol. 25. No. 19. pp. 2895-2900.
ГОСТ со всеми авторами (до 50) Скопировать
Polyak F., Dorofeeva T., Zelchan G. Catalytic Hydrogenation of Chiral 2-(2-Furyl)-3,4-dimethyl-5-phenyloxazolidine // Synthetic Communications. 1995. Vol. 25. No. 19. pp. 2895-2900.
RIS |
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TY - JOUR
DO - 10.1080/00397919508011419
UR - https://doi.org/10.1080/00397919508011419
TI - Catalytic Hydrogenation of Chiral 2-(2-Furyl)-3,4-dimethyl-5-phenyloxazolidine
T2 - Synthetic Communications
AU - Polyak, Felix
AU - Dorofeeva, Tatiana
AU - Zelchan, Gunar
PY - 1995
DA - 1995/10/01
PB - Taylor & Francis
SP - 2895-2900
IS - 19
VL - 25
SN - 0039-7911
SN - 1532-2432
ER -
BibTex |
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BibTex (до 50 авторов) Скопировать
@article{1995_Polyak,
author = {Felix Polyak and Tatiana Dorofeeva and Gunar Zelchan},
title = {Catalytic Hydrogenation of Chiral 2-(2-Furyl)-3,4-dimethyl-5-phenyloxazolidine},
journal = {Synthetic Communications},
year = {1995},
volume = {25},
publisher = {Taylor & Francis},
month = {oct},
url = {https://doi.org/10.1080/00397919508011419},
number = {19},
pages = {2895--2900},
doi = {10.1080/00397919508011419}
}
MLA
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Polyak, Felix, et al. “Catalytic Hydrogenation of Chiral 2-(2-Furyl)-3,4-dimethyl-5-phenyloxazolidine.” Synthetic Communications, vol. 25, no. 19, Oct. 1995, pp. 2895-2900. https://doi.org/10.1080/00397919508011419.