Dienamines as diels-alder dienes. An efficient synthesis of a key intermediate for drimane-related sesquiterpenes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
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2. The stereospecific synthesis of D,L-Winterin
3. Pyrolytic aromatization of 3,5,6,7,8,8a-hexahydro-5,5,8a-trimethyl-1,2-naphthalenedicarboxylate
4. Stereospecific total synthesis of (.+-.)-warburganal and related compounds
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1. Diels-Alder reactions of 1-amino-1,3-dienes and related systems;Tetrahedron;2021-08
2. Oppolzer-Type Intramolecular Diels–Alder Cycloadditions via Isomerizations of Allenamides;Organic Letters;2011-05-25
3. 2,2,2-Trichloroethyltrans-1,3-Butadiene-1-carbamate;Encyclopedia of Reagents for Organic Synthesis;2001-04-15
4. High pressure Diels Alder reactions of 1-Vinyl-2,2,6-trimethylcyclohexene catalyzed by chiral lewis acids; an enantioselective route to a drimane sesquiterpene precursor;Tetrahedron: Asymmetry;1995-05
5. Acyclic isoprenoid 1,3-dieneamines in the Diels-Alder reaction;Bulletin of the Academy of Sciences of the USSR Division of Chemical Science;1991-05
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