Synthesis of Tetracyclic Heterocompounds as Selective Estrogen Receptor Modulators. Part 2. Process Improvement for Scale-Up Of 2,5,8-Substituted 11,12-Dihydro-5H-6,13-dioxabenzo[3,4]cyclohepta-[1,2-a]naphthalene Derivatives-Reference-Cited by-同舟云学术

Synthesis of Tetracyclic Heterocompounds as Selective Estrogen Receptor Modulators. Part 2. Process Improvement for Scale-Up Of 2,5,8-Substituted 11,12-Dihydro-5H-6,13-dioxabenzo[3,4]cyclohepta-[1,2-a]naphthalene Derivatives

Published:2007-06-21 Issue:4 Volume:11 Page:731-738
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Li Xun¹,Reuman Michael¹,Russell Ronald K.¹,Youells Scott¹,Beish Sandra¹,Hu Zhiyong¹,Branum Shawn¹,Jain Nareshkumar¹,Sui Zhihua¹

Affiliation:

1. Johnson & Johnson Pharmaceutical Research & Development, L.L.C., U.S. Research & Early Development, 1000 Route 202, Raritan, New Jersey 08869, U.S.A.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/op700061x

Reference17 articles.

1. Synthesis of novel tetracyclic chromenes through carbanion chemistry of 4-methyl coumarins

2. Novel Chromene-Derived Selective Estrogen Receptor Modulators Useful for Alleviating Hot Flushes and Vaginal Dryness

3. A facile synthesis of an unsymmetric benzopyranobenzopyran ring system

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