Efficient Synthesis of 1-Amino-2-naphthalenecarboxylic Acid Derivatives via a Sequential Michael Addition/Enolate−Nitrile Coupling Route and Its Application to Facile Preparation of 9-Amino Analogues of Arylnaphthofuranone Lignans-Reference-Cited by-同舟云学术

Efficient Synthesis of 1-Amino-2-naphthalenecarboxylic Acid Derivatives via a Sequential Michael Addition/Enolate−Nitrile Coupling Route and Its Application to Facile Preparation of 9-Amino Analogues of Arylnaphthofuranone Lignans

Published:1997-02-01 Issue:3 Volume:62 Page:664-668
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Kobayashi Kazuhiro¹,Uneda Tomokazu¹,Takada Keiichiro¹,Tanaka Hiroto¹,Kitamura Tomohide¹,Morikawa Osamu¹,Konishi Hisatoshi¹

Affiliation:

1. Department of Materials Science, Faculty of Engineering, Tottori University, Tottori 680, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo961744r

Reference24 articles.

1. A simple synthesis of compounds with the benz[h]imidazo[1,2-c]quinazoline ring system

2. Ring Closure of Ylidenemalononitriles. III.1 Formation of Six-Membered Rings and Related Chemistry2

3. New general synthesis of tert-butyl 3-amino-2-naphthalenecarboxylates by an electrocyclic reaction of o-quinonedimethides generated from tert-butyl (Z)-3-amino-3-(bicyclo[4.2.0]octa-1,3,5-trien-7-yl)prop-2-enoates

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