Pre-activation protocol leading to highly stereoselectivity-controllable glycosylations of oxazolidinone protected glucosamines

Chemical Communications : Chem Comm
Yiqun GengXin-Shan Ye

Abstract

Under pre-activation glycosylation conditions, the 4,6-di-O-acetyl-N-acetyloxazolidinone protected donor afforded either excellent beta- or alpha-stereoselectivity simply by means of the addition of hindered base TTBP or the absence of base, leading to the controllable stereochemistry of coupling reactions.

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Citations

Sep 30, 2009·Chemical Communications : Chem Comm·Martin A FascioneW Bruce Turnbull
Oct 22, 2011·Carbohydrate Research·Jianhao FengChang-Chun Ling
Oct 3, 2008·Carbohydrate Research·Guohua WeiYuguo Du
Nov 6, 2015·Organic Letters·Run-Ze MaoXin-Shan Ye
Jun 18, 2009·Chemistry : a European Journal·Shino ManabeYukishige Ito
Jul 4, 2012·Chemistry, an Asian Journal·Ramu EnugalaM Manuel B Marques
May 29, 2012·Chemistry, an Asian Journal·Hiromichi FujiokaKenichi Murai
Jun 11, 2014·Chemical Record : an Official Publication of the Chemical Society of Japan ... [et Al.]·Shino Manabe, Yukishige Ito
Apr 11, 2015·Organic & Biomolecular Chemistry·Baolin WuTiehai Li
Jun 6, 2009·Journal of the American Chemical Society·Enoch A Mensah, Hien M Nguyen
Jun 18, 2017·Chemistry : a European Journal·Gao-Lan ZhangXin-Shan Ye
Oct 23, 2010·Molecules : a Journal of Synthetic Chemistry and Natural Product Chemistry·Jian Guo, Xin-Shan Ye
Apr 18, 2012·Beilstein Journal of Organic Chemistry·Toshiki NokamiJun-Ichi Yoshida
May 29, 2018·European Journal of Organic Chemistry·Bo YangXuefei Huang
Feb 10, 2021·Organic Letters·Wenbin ShangChengfeng Xia
Aug 21, 2008·The Journal of Organic Chemistry·Johan D M OlssonStefan Oscarson
Oct 27, 2020·The Journal of Organic Chemistry·Robin A JeanneretM Carmen Galan
Jun 29, 2018·Chemical Reviews·Matteo PanzaAlexei V Demchenko

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