Enantioselective synthesis of a 5-LO inhibiting hydroxyurea. Construction of the dihydro-benzofuran nucleus by tandem nucleophilic addition and intramolecular cyclization-Reference-Cited by-同舟云学术

Enantioselective synthesis of a 5-LO inhibiting hydroxyurea. Construction of the dihydro-benzofuran nucleus by tandem nucleophilic addition and intramolecular cyclization

Published:1996-07 Issue:27 Volume:37 Page:4639-4642
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Flisak Joseph R.,Lantos Ivan,Liu Li,Matsuoka Richard T.,Mendelson Wilford L.,Tucker Lynn M.,Villani Anthony J.,Zhang Wei-Yuan

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference13 articles.

1. Structure-activity analysis of a class of orally active hydroxamic acid inhibitors of leukotriene biosynthesis

2. Addition of Organometallic Reagents to N-Glycosyl Nitrones. Enantioselective Syntheses of (+)-(R)- and (-)-(S)-Zileuton

3. Enantioselective synthesis of 5-LO inhibitors using a gulofuranose auxiliary

4. Resolution of hydroxyureas

5. Diastereoselectivity of organometallic additions to nitrones bearing stereogenic N-substituents

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