An Efficient Protocol for Selective Silylation of Hydroxy Group Using N,O-Bis(tert-butyldimethylsilyl)acetamide and N,N-Dimethyl-4-aminopyridine N-Oxide-Reference-Cited by-同舟云学术

An Efficient Protocol for Selective Silylation of Hydroxy Group Using N,O-Bis(tert-butyldimethylsilyl)acetamide and N,N-Dimethyl-4-aminopyridine N-Oxide

Published:2022-09-05 Issue:9 Volume:51 Page:953-956
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Mandai Hiroki¹,Matsuura Yuichiro²,Johari Fatin Mahfuzah Binti²,Mitsudo Koichi²,Suga Seiji²

Affiliation:

1. Department of Pharmacy, Faculty of Pharmacy, Gifu University of Medical Science, 4-3-3 Nijigaoka, Kani, Gifu 509-0293, Japan

2. Division of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University, 3-1-1 Tsushima-naka Kita-ku, Okayama 700-8530, Japan

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

http://www.journal.csj.jp/doi/pdf/10.1246/cl.220281

Reference43 articles.

1. Protection for the Hydroxyl Group, Including 1,2- and 1,3-Diols in Greene's Protective Groups in Organic Synthesis, 5th ed, ed by P. G. M. Wuts, John Wiley & Sons, Inc., Hoboken, 2014, pp. 201.

2. Modified guanidines as chiral superbases: the first example of asymmetric silylation of secondary alcohols

3. Enantioselective silyl protection of alcohols catalysed by an amino-acid-based small molecule

4. Kinetic Resolution of 1,2-Diols through Highly Site- and Enantioselective Catalytic Silylation

5. Regiodivergent Reactions through Catalytic Enantioselective Silylation of Chiral Diols. Synthesis of Sapinofuranone A

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