Affiliation:
1. School of Materials Science and Chemical Engineering Institute of Drug Discovery Technology Ningbo University Ningbo 315211 P. R. China
2. State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics Innovation Academy for Precision Measurement Science and Technology Chinese Academy of Sciences Wuhan 430071 P. R. China
Abstract
AbstractThe first direct and selective 3,6‐di‐thiolation and 3,6‐di‐selenylation of carbazoles using diaryl disulfides/diselenide as the sulfur/selenium source were demonstrated. This simple, general, and efficient method could deliver a wide range of 3,6‐di‐sulfenyl‐carbazoles and 3,6‐di‐selenyl‐carbazoles from readily available starting materials with high regioselectivity in an easily‐operated one‐step reaction via a Ag/K2S2O8‐mediated protocol.
Funder
Natural Science Foundation of Ningbo
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Cited by
5 articles.
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