Simple syntheses of L-fucopyranose and fucosidase inhibitors utilizing the highly stereoselective methylation of an arabinofuranoside 5-urose derivative
Тип публикации: Journal Article
Дата публикации: 1997-01-01
SJR: —
CiteScore: —
Impact factor: —
ISSN: 0300922X, 13645463, 14727781
General Medicine
Краткое описание
The simple syntheses of L-fucopyranose 1 and its three
analogues 2–4 are described. A key reaction is a stereocontrolled
elongation by one carbon unit at the side chain of an
α-D-arabino-pentodialdo-1,4-furanoside 9 with
MeMgI–ZnCl2 or Me3Al. Diastereofacial
selectivities of more than 92% were achieved.
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ГОСТ
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Takahashi S., Kuzuhara H. Simple syntheses of L-fucopyranose and fucosidase inhibitors utilizing the highly stereoselective methylation of an arabinofuranoside 5-urose derivative // Journal of the Chemical Society Perkin Transactions 1. 1997. Vol. 5. pp. 607-612.
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Takahashi S., Kuzuhara H. Simple syntheses of L-fucopyranose and fucosidase inhibitors utilizing the highly stereoselective methylation of an arabinofuranoside 5-urose derivative // Journal of the Chemical Society Perkin Transactions 1. 1997. Vol. 5. pp. 607-612.
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TY - JOUR
DO - 10.1039/a606564c
UR - https://doi.org/10.1039/a606564c
TI - Simple syntheses of L-fucopyranose and fucosidase inhibitors utilizing the highly stereoselective methylation of an arabinofuranoside 5-urose derivative
T2 - Journal of the Chemical Society Perkin Transactions 1
AU - Takahashi, Shunya
AU - Kuzuhara, Hiroyoshi
PY - 1997
DA - 1997/01/01
PB - Royal Society of Chemistry (RSC)
SP - 607-612
IS - 5
SN - 0300-922X
SN - 1364-5463
SN - 1472-7781
ER -
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@article{1997_Takahashi,
author = {Shunya Takahashi and Hiroyoshi Kuzuhara},
title = {Simple syntheses of L-fucopyranose and fucosidase inhibitors utilizing the highly stereoselective methylation of an arabinofuranoside 5-urose derivative},
journal = {Journal of the Chemical Society Perkin Transactions 1},
year = {1997},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://doi.org/10.1039/a606564c},
number = {5},
pages = {607--612},
doi = {10.1039/a606564c}
}