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New Chirones Prepared from 2-Acetoxyglucal

Alexander Genrikhovich Tolstikov 1
Alexander Genrikhovich Tolstikov
, 
Elena E Savateeva 2
Elena E Savateeva
, 
Leonid Vasilevich Spirikhin 2
Leonid Vasilevich Spirikhin
, 
Genrikh Alexandrovich Tolstikov 3
Genrikh Alexandrovich Tolstikov
10.1070/MC1991v001n04ABEH000082
Published 1991-12-31
Communication , Volume 1, Issue 4, 133-134
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Tolstikov A. G. et al. New Chirones Prepared from 2-Acetoxyglucal // Mendeleev Communications. 1991. Vol. 1. No. 4. pp. 133-134.
GOST all authors (up to 50) Copy
Tolstikov A. G., Savateeva E. E., Spirikhin L. V., Tolstikov G. A. New Chirones Prepared from 2-Acetoxyglucal // Mendeleev Communications. 1991. Vol. 1. No. 4. pp. 133-134.
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TY - JOUR
DO - 10.1070/MC1991v001n04ABEH000082
UR - https://mendcomm.colab.ws/publications/10.1070/MC1991v001n04ABEH000082
TI - New Chirones Prepared from 2-Acetoxyglucal
T2 - Mendeleev Communications
AU - Tolstikov, Alexander Genrikhovich
AU - Savateeva, Elena E
AU - Spirikhin, Leonid Vasilevich
AU - Tolstikov, Genrikh Alexandrovich
PY - 1991
DA - 1991/12/31
PB - Mendeleev Communications
SP - 133-134
IS - 4
VL - 1
ER -
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@article{1991_Tolstikov,
author = {Alexander Genrikhovich Tolstikov and Elena E Savateeva and Leonid Vasilevich Spirikhin and Genrikh Alexandrovich Tolstikov},
title = {New Chirones Prepared from 2-Acetoxyglucal},
journal = {Mendeleev Communications},
year = {1991},
volume = {1},
publisher = {Mendeleev Communications},
month = {Dec},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1991v001n04ABEH000082},
number = {4},
pages = {133--134},
doi = {10.1070/MC1991v001n04ABEH000082}
}
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Tolstikov, Alexander Genrikhovich, et al. “New Chirones Prepared from 2-Acetoxyglucal.” Mendeleev Communications, vol. 1, no. 4, Dec. 1991, pp. 133-134. https://mendcomm.colab.ws/publications/10.1070/MC1991v001n04ABEH000082.

Abstract

Reaction of 2,3,4,6-tetra-O-acetyl-D-glucal with allyltrimethylsilane, methyl 3-mercaptopropionate, methyl (6R)-6-benzoyloxy-7-oxyheptanoate or glycolic acid methyl ester, catalysed by boron trifluride etherate, leads preferentially to the a-anomers of unsaturated 2’-oxo-C-, S- or O-glycosides.

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