Acid- and isobutylene-free synthesis of t-butyl ethers by in situ formation of 2-t-butoxy-1-methylpyridinium triflate-Reference-Cited by-同舟云学术

Acid- and isobutylene-free synthesis of t-butyl ethers by in situ formation of 2-t-butoxy-1-methylpyridinium triflate

Published:2014-12 Issue:51 Volume:55 Page:7133-7135
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Salvati Anna E.,Hubley Christian T.,Albiniak Philip A.

Funder

Ball State University

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference28 articles.

1. (a) 2-Benzyloxy-1-methylpyridinium triflate [26189-59-3] is licensed, manufactured, and distributed non-exclusively by Sigma–Aldrich Chemical Co., catalog #679674; see: Dudley, G. B. Compounds and methods of arylmethylation (benzylation) as protection for alcohol groups. U.S. Patent Appl. 11/399,300, 2006; (b) ChemFiles 2007, 7.

2. Mix-and-Heat Benzylation of Alcohols Using a Bench-Stable Pyridinium Salt

3. PROTECTION OF ALCOHOLS USING 2-BENZYLOXY-1-METHYLPYRIDINIUM TRIFLUOROMETHANESULFONATE: METHYL (R)-(-)-3-BENZYLOXY-2-METHYL PROPANOATE

4. Synthesis of Benzyl Esters Using 2-Benzyloxy-1-methylpyridinium Triflate

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