A Novel Two-Carbon Homologation with N-Vinylacetamides and Ethyl Vinyl Ether as Acetaldehyde Anion Equivalents in the Synthesis of 9H-Xanthene, 9H-Thioxanthene, and 9,10-Dihydro-9-acridine Carboxaldehydes-Reference-Cited by-同舟云学术

A Novel Two-Carbon Homologation with N-Vinylacetamides and Ethyl Vinyl Ether as Acetaldehyde Anion Equivalents in the Synthesis of 9H-Xanthene, 9H-Thioxanthene, and 9,10-Dihydro-9-acridine Carboxaldehydes

Published:2003-12-20 Issue:2 Volume:69 Page:584-586
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Prashad Mahavir¹,Lu Yansong¹,Repič Oljan¹

Affiliation:

1. Process Research and Development, Chemical and Analytical Development, Novartis Institute for Biomedical Research, One Health Plaza, East Hanover, New Jersey 07936 mahavir.prashad@pharma.novartis.com

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0303057

Reference13 articles.

1. Design, synthesis and preliminary evaluation of novel 3′-Substituted carboxycyclopropylglycines as antagonists at group 2 metabotropic glutamate receptors

2. A novel approach to tricyclic pharmaceuticals via directed dilithiation of diaryl compounds

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

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