An enantio- and stereocontrolled synthesis of (–)-mycestericin E via cinchona alkaloid-catalyzed asymmetric Baylis–Hillman reaction
Тип публикации: Journal Article
Дата публикации: 2001-01-01
SCImago Q1
WOS Q2
БС1
SJR: 0.907
CiteScore: 7.2
Impact factor: 4.3
ISSN: 13597345, 1364548X
PubMed ID:
12240274
Materials Chemistry
Metals and Alloys
Surfaces, Coatings and Films
General Chemistry
Ceramics and Composites
Electronic, Optical and Magnetic Materials
Catalysis
Краткое описание
A new enantiocontrolled synthesis of a potent immunosuppressant(-)-mycestericin E has been accomplished by using cinchona alkaloid-catalyzed asymmetric Baylis-Hillman reaction of an aldehyde with 1,1,1,3,3,3-hexafluoroisopropyl acrylate and Lewis acid-promoted cyclisation of an epoxytrichloroacetimidate as the key steps.
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137
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ГОСТ
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Iwabuchi Y. et al. An enantio- and stereocontrolled synthesis of (–)-mycestericin E via cinchona alkaloid-catalyzed asymmetric Baylis–Hillman reaction // Chemical Communications. 2001. Vol. 19. pp. 2030-2031.
ГОСТ со всеми авторами (до 50)
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Iwabuchi Y., Furukawa M., Esumi T., Hatakeyama S. An enantio- and stereocontrolled synthesis of (–)-mycestericin E via cinchona alkaloid-catalyzed asymmetric Baylis–Hillman reaction // Chemical Communications. 2001. Vol. 19. pp. 2030-2031.
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RIS
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TY - JOUR
DO - 10.1039/b106471c
UR - https://doi.org/10.1039/b106471c
TI - An enantio- and stereocontrolled synthesis of (–)-mycestericin E via cinchona alkaloid-catalyzed asymmetric Baylis–Hillman reaction
T2 - Chemical Communications
AU - Iwabuchi, Yoshiharu
AU - Furukawa, Mariko
AU - Esumi, Tomoyuki
AU - Hatakeyama, Susumi
PY - 2001
DA - 2001/01/01
PB - Royal Society of Chemistry (RSC)
SP - 2030-2031
IS - 19
PMID - 12240274
SN - 1359-7345
SN - 1364-548X
ER -
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BibTex (до 50 авторов)
Скопировать
@article{2001_Iwabuchi,
author = {Yoshiharu Iwabuchi and Mariko Furukawa and Tomoyuki Esumi and Susumi Hatakeyama},
title = {An enantio- and stereocontrolled synthesis of (–)-mycestericin E via cinchona alkaloid-catalyzed asymmetric Baylis–Hillman reaction},
journal = {Chemical Communications},
year = {2001},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://doi.org/10.1039/b106471c},
number = {19},
pages = {2030--2031},
doi = {10.1039/b106471c}
}
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