Effect of Methoxyl Group Position on the Regioselectivity of Ammonia Substitution Reactions Involving 3,3‘-Dichloro-2,2‘-binaphthoquinones-Reference-Cited by-同舟云学术

Effect of Methoxyl Group Position on the Regioselectivity of Ammonia Substitution Reactions Involving 3,3‘-Dichloro-2,2‘-binaphthoquinones

Published:2004-06-23 Issue:15 Volume:69 Page:5128-5131
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Stagliano Kenneth W.¹,Lu Zhenhai¹,Emadi Ashkan¹,Harwood John S.¹,Harwood Cynthia A.¹

Affiliation:

1. Department of Biological, Chemical, and Physical Sciences, Illinois Institute of Technology, Chicago, Illinois 60616, and Department of Chemistry, University of Illinois at Chicago, Chicago, Illinois 60607 stagliano@iit.edu

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo049713g

Reference21 articles.

1. HIV inhibitory natural products. 11. Structure, absolute stereochemistry, and synthesis of conocurvone, a potent, novel HIV-inhibitory naphthoquinone trimer from a Conospermum sp

2. 4,4'-Bi(cyclobutene-1,2-diones): bisquaryls

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