Reactivity insights from the allylation of substituted phenols with 2-allyloxy-1-methylpyridinium triflate

Author:

Jacobs Andrew M.,Winters Aaliyah C.,Albiniak Philip A.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference26 articles.

1. Discussion addendum for protection of alcohols using 2-benzyloxy-1-methylpyridinium trifluoro-methane-sulfonate: methyl (R)-(-)-3-benzyloxy-2-methyl propanoate;Fulo;Org. Synth.,2019

2. (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.

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

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