Stereochemical preferences and requirement for the 3-hydroxyl group in novel anticonvulsant 4-fluorobenzoylamino benzopyrans-Reference-Cited by-同舟云学术

Stereochemical preferences and requirement for the 3-hydroxyl group in novel anticonvulsant 4-fluorobenzoylamino benzopyrans

Published:1995-11 Issue:21 Volume:5 Page:2563-2566
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Brown Thomas H.,Campbell Colin A.,Chan Wai N.,Evans John M.,Martin Roger T.,Stean Tania O.,Stemp Geoffrey,Stevens Nichola C.,Thompson Mervyn,Upton Neil,Vong Antonio K.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference5 articles.

1. Stereochemical differentiation of anticonvulsant and antihypertensive effects in 4-(fluorobenzoylamino)-benzopyrans

2. Synthesis and antihypertensive activity of 4-(cyclic amido)-2H-1-benzopyrans

3. The action of diethylaminosulphur trifluoride (dast) on trans-4-amido- 3-Chromanols: Preparation of cis-amidoalcohols via oxazolines

4. New fluorinating reagents. Dialkylaminosulfur fluorides

5. Modern methods for the introduction of fluorine into organic molecules: an approach to compounds with altered chemical and biological activities

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