Diphenyl Disulfide and Sodium in NMP as an Efficient Protocol for in Situ Generation of Thiophenolate Anion: Selective Deprotection of Aryl Alkyl Ethers and Alkyl/Aryl Esters under Nonhydrolytic Conditions,-Reference-Cited by-同舟云学术

Diphenyl Disulfide and Sodium in NMP as an Efficient Protocol for in Situ Generation of Thiophenolate Anion: Selective Deprotection of Aryl Alkyl Ethers and Alkyl/Aryl Esters under Nonhydrolytic Conditions,

Published:2002-02-14 Issue:6 Volume:67 Page:1776-1780
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Chakraborti Asit K.¹,Nayak Mrinal K.¹,Sharma Lalima¹

Affiliation:

1. Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research (NIPER), Sector 67, S. A. S. Nagar 160 062, India

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo010611p

Reference44 articles.

1. Protective Groups in Organic Synthesis

2. Chemoselective O-methylation of phenols under non-aqueous condition

3. Chemoselective Protection of Carboxylic Acid as Methyl Ester: A Practical Alternative to Diazomethane Protocol

4. Cleavage of Ethers

5. Selective Dealkylations of Aryl Alkyl Ethers, Thioethers, and Selenoethers

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