2-Butyl-4-iodoimidazole-5-carboxaldehyde: A Versatile Intermediate for the Synthesis of Highly Functionalized Imidazoles-Reference-Cited by-同舟云学术

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2-Butyl-4-iodoimidazole-5-carboxaldehyde: A Versatile Intermediate for the Synthesis of Highly Functionalized Imidazoles

Published:1993-12 Issue:22 Volume:23 Page:3231-3248
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Wittenberger Steven J.¹,Tasker Andrew²,Sorensen Bryan K.²,Donner B. Gregory²

Affiliation:

1. a Process Chemistry D-45L/AP10, Pharmaceutical Products Division Abbott Laboratories , One Abbott Park Road, Abbott Park, IL, 60064-3500

2. b Cardiovascular Chemistry D-47C/AP10, Pharmaceutical Products Division, Abbott Laboratories , One Abbott Park Road, Abbott Park, IL, 60064-3500

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397919308011184

Reference15 articles.

1. The discovery of DuP 753, a potent, orally active nonpeptide angiotensin II receptor antagonist

2. Patent Update: Angiotensin-II Antagonists: Patent Activity since the Discovery of DuP-753

3. Discovery of a novel class of orally active, non-peptide angiotensin II antagonists

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Synthesis, structure–activity relationship studies, and identification of novel 5,6,7,8-tetrahydroimidazo[1,5-a]pyrazine derivatives as dual orexin receptor antagonists. Part 1;Bioorganic & Medicinal Chemistry Letters;2013-04

2. The discovery of new potent non-peptide Angiotensin II AT1 receptor blockers: A concise synthesis, molecular docking studies and biological evaluation of N-substituted 5-butylimidazole derivatives;European Journal of Medicinal Chemistry;2012-09

3. ChemInform Abstract: 2-Butyl-4-iodoimidazole-5-carboxaldehyde: A Versatile Intermediate for the Synthesis of Highly Functionalized Imidazoles.;ChemInform;2010-08-19

4. Large-Scale Oxidations in the Pharmaceutical Industry;Chemical Reviews;2006-06-27

5. Preparation of a clinically investigated ras farnesyl transferase inhibitor;Journal of Heterocyclic Chemistry;2003-03

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