Generation of chiral N-acylpyridinium ions by means of silyl triflates and their diastereoselective trapping reactions: formation of N-acyldihydropyridines and N-acyldihydropyridones-Reference-Cited by-同舟云学术

Generation of chiral N-acylpyridinium ions by means of silyl triflates and their diastereoselective trapping reactions: formation of N-acyldihydropyridines and N-acyldihydropyridones

Published:2002-08 Issue:33 Volume:58 Page:6757-6770
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Hoesl Cornelia E,Maurus Markus,Pabel Jörg,Polborn Kurt,Wanner Klaus Th

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference30 articles.

1. Reaction of allylic tin reagents with nitrogen heteroaromatics activated by alkyl chloroformates: regioselective synthesis of .alpha.-allylated 1,2-dihydropyridines and change of the regioselectivity depending on methyl substituents at the allylic moiety

2. Regioselective addition of Grignard reagents to 1-acylpyridinium salts. A convenient method for the synthesis of 4-alkyl(aryl)pyridines

3. A novel hypervalent antimony ate complex (12-Sb-6)

4. Synthesis of 4-Silyl-substituted Methyl Nicotinates via Silylcupration of N-Acylpyridinium Salts

5. New Developments in the Chemistry of N-Acyliminium Ions and Related Intermediates

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