Nucleophilic Displacement at Benzhydryl Centers: Asymmetric Synthesis of 1,1-Diarylalkyl Derivatives-Reference-Cited by-同舟云学术

Nucleophilic Displacement at Benzhydryl Centers: Asymmetric Synthesis of 1,1-Diarylalkyl Derivatives

Published:2003-12-13 Issue:1 Volume:6 Page:111-114
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Bolshan Yuri¹,Chen Cheng-yi¹,Chilenski Jennifer R.¹,Gosselin Francis¹,Mathre David J.¹,O'Shea Paul D.¹,Roy Amélie¹,Tillyer Richard D.¹

Affiliation:

1. Department of Process Research, Merck Frosst Centre for Therapeutic Research, P.O. Box 1005, Pointe Claire-Dorval, Québec, H9R 4P8, Canada, and Department of Process Research, Merck Research Laboratories, P.O. Box 2000, Rahway, New Jersey 07065, USA

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol0361655

Reference23 articles.

1. Tolterodine – a new bladder-selective antimuscarinic agent

2. Nontricyclic antidepressant agents derived from cis- and trans-1-amino-4-aryltetralins

3. Selective ETA Antagonists. 5. Discovery and Structure−Activity Relationships of Phenoxyphenylacetic Acid Derivatives

4. Asymmetric Synthesis of CDP840 by Jacobsen Epoxidation. An Unusual Syn Selective Reduction of an Epoxide

5. Sulfur-Ylide-Mediated Synthesis of Functionalized and Trisubstituted Epoxides with High Enantioselectivity; Application to the Synthesis of CDP-840

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