Synthesis of 8-azaprostaglandin E1 and E2
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference5 articles.
1. Synthesis of 11-desoxy-8-azaprostaglandin E1
2. Sulfoxide-Carbodiimide Reactions. I. A Facile Oxidation of Alcohols
3. Sulfoxide-Carbodiimide Reactions. II. Scope of the Oxidation Reaction1
4. Stereo-controlled synthesis of dl-prostaglandins F2.alpha. and E2
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1. Difluoromethylene at the γ-Lactam α-Position Improves 11-Deoxy-8-aza-PGE1 Series EP4 Receptor Binding and Activity: 11-Deoxy-10,10-difluoro-8-aza-PGE1 Analog (KMN-159) as a Potent EP4 Agonist;Journal of Medicinal Chemistry;2019-04-09
2. A Facile Route for the Synthesis of Novel Heterocyclic Prostaglandin F2αAnalogs;Journal of Heterocyclic Chemistry;2014-01-23
3. Synthesis of a novel prostaglandin containing heteroatoms in the ring cyclopentane;Tetrahedron Letters;2001-12
4. Stereocontrolled preparation of chiral secondary α-methylene γ-lactams by addition of organozinc reagents derived from 2-(bromomethy])acrylates to imines using β-aminoalcohols as chiral auxiliaries.;Tetrahedron: Asymmetry;1992-04
5. Synthesis and spectroscopic properties of long-chain aza, aziridine and azetidine fatty esters;Journal of the American Oil Chemists' Society;1992-04
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