@inbook{9b2825191ac841ca9d2af7ce3edcf65c,
title = "Synthesis of 1,3,4,6-Tetra-O-acetyl-α-D-glucopyranose Revisited",
author = "Alexei Demchenko",
note = "Contents: Section I: Synthetic MethodsHighly Stereoselective 1,2-cis-Glycosylations Employing C-2 (S)-(Phenylthiomethyl)benzyl Ether as a Chiral AuxiliaryThomas J. Boltje, Randy Benedict, and Geert-Jan BoonsRegioselective Reductive Openings of 4,6-O-Benzylidene-Type Acetals Using LiAlH4-AlCl3Mihaly Herczeg, Laszlo Lazar, Markus Ohlin, and Aniko BorbasA Facile Method for Oxidation of Primary Alcohols to Carboxylic Acids in Carbohydrate SynthesisZhaojun Yin, Steven Dulaney, Gopinath Tiruchinapally, Bo Yang, Guitao Wang and Xuefei HuangUltrasonic Energy Promoted Allylation to Generate 1-C-(2,3,4,6-Tetra-O-benzyl- -d-glucopyranosyl)prop-2-eneMark Farrell, Ciaran O'Reilly, Dilip V.",
year = "2014",
language = "American English",
booktitle = "CARBOHYDRATE CHEMISTRY : proven synthetic methods, volume 2.",
}