A convenient and highly stereoselective synthesis of 14-substituted 8,13-diazaoestrone analogues by domino ring closures
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference24 articles.
1. A new and convenient synthesis of 13,16-diazaestrone analogs
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3. Novel High Energy Intermediate Analogues with Triazasterol-related Structures as Inhibitors of the Ergosterol Biosynthesis V [1]. Synthesis of Hexahydro-5H-imidazo[1?, 2?: 1,2]pyrimido-[4,3-a]isoquinolines and 1-Alkyl Analogues Representing New 8,13,15-Triazasteroids
4. The domino intramolecular Diels–Alder approach to 16-oxasteroids
5. Synthesis of the first monoaromatic B-ring 13-azasteroid ring system by sequential angular annulation
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1. An overview of synthetic approaches for heterocyclic steroids;Tetrahedron;2013-04
2. l-Proline derived nitrogenous steroidal systems: an asymmetric approach to 14-azasteroids;RSC Advances;2013
3. Stereoselective synthesis and structural analysis of polycyclic lactams derived from tetrahydroisoquinoline 1,2- and 1,3-diamines;Arkivoc;2012-05-01
4. Synthesis and structural analysis of tetra- and pentacyclic lactams derived from regioisomeric tetrahydroisoquinoline diamines;Journal of Molecular Structure;2010-11
5. Facile synthesis of vicinal diamines via oxidation of N-phenyltetrahydroisoquinolines with DDQ;Tetrahedron Letters;2009-03
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