Stereospecific 1,4-Addition of Organolithium Reagents to Unprotected 1- and 2-Naphthalenecarboxylic Acids. A Facile Route to 1,1,2- and -1,2,2-Trisubstituted 1,2-Dihydronaphthalenes-Reference-Cited by-同舟云学术

Stereospecific 1,4-Addition of Organolithium Reagents to Unprotected 1- and 2-Naphthalenecarboxylic Acids. A Facile Route to 1,1,2- and -1,2,2-Trisubstituted 1,2-Dihydronaphthalenes

Published:1996-01-01 Issue:16 Volume:61 Page:5206-5207
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Plunian Barbara¹,Mortier Jacques¹,Vaultier Michel¹,Toupet Loïc²

Affiliation:

1. Université Rennes-I, Groupe de recherches de physicochimie structurale, unité associée au CNRS no. 704, avenue du Général Leclerc, 35042 Rennes Cedex, France

2. Université Rennes-I, Groupe de physique cristalline, unité associée au CNRS no. 15, avenue du Général Leclerc, 35042 Rennes Cedex, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo960934z

Reference20 articles.

1. Asymmetric conjugate addition

2. MICHAEL ADDITION OF ORGANOLITHIUM COMPOUNDS. A REVIEW

3. Tritylketone und Tritylenone. Beiträge zur sterisch erzwungenenMichael-Addition und zur diastereoselektiven Aldol-Addition

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