Regio- and chemoselective addition of alkynyltin reagents to the 2-position of 3-acylpyridines activated by methyl chloroformate: selective synthesis of 2,3-disubstituted 1,2-dihydropyridines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference24 articles.
1. Chemistry of dihydropyridines
2. Recent advances in the chemistry of dihydropyridines
3. Highly Regioselective α-Addition of Alkynyl and Alkenyl Grignard Reagents to 1-Alkoxycarbonylpyridinium Salts and Its Application to Synthesis of 1-Azabicycloalkanes and (±)-Solenopsin A
4. Highly regioselective .alpha.-allylation of N-(alkoxycarbonyl)pyridinium salts by means of allyltin reagents
5. An efficient regio- and stereoselective synthesis of (.+-.)-monomorine I via the highly regioselective .alpha.-alkynylation of a 1-acylpyridinium salt
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3. Regioselective Nucleophilic Addition of Organometallic Reagents to 3-Geminal Bis(silyl) N-Acyl Pyridinium;Organic Letters;2014-03-25
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