Development of an Efficient and Stereoselective Manufacturing Route to Idoxifene-Reference-Cited by-同舟云学术

Development of an Efficient and Stereoselective Manufacturing Route to Idoxifene

Published:2001-08-22 Issue:5 Volume:5 Page:479-490
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Ace Karl W.¹,Armitage Mark A.¹,Bellingham Richard K.¹,Blackler Paul D.¹,Ennis David S.¹,Hussain Nigel¹,Lathbury David C.¹,Morgan David O.¹,O'Connor Noah¹,Oakes Graham H.¹,Passey Stephen C.¹,Powling Laurence C.¹

Affiliation:

1. Chemical Development, GlaxoSmithKline Pharmaceuticals, Old Powder Mills, Nr. Leigh, Tonbridge, Kent TN11 9AN, U.K.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/op0100394

Reference34 articles.

1. Derivatives of tamoxifen. Dependence of antiestrogenicity on the 4-substituent

2. Variation of the inhibition of calmodulin dependent cyclic AMP phosphodiesterase amongst analogues of tamoxifen; Correlations with cytotoxicity

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