Stereoselectivity in intramolecular Diels-Alder reaction II: Influence of alkyl substituent on cyclization of azatrienes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
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2. AN EFFICIENT METHOD FOR THE STEREOSELECTIVE SYNTHESIS OF TRICYCLIC COMPOUNDS—THE INTRAMOLECULAR DIELS–ALDER REACTION OF CYCLIC α,β-UNSATURATED CARBOXAMIDES—
3. Synthesis of elusive 1,4-dihydrocarbazoles via intramolecular trapping of an indole-2,3-quinodimethane
4. A stereoselective total synthesis of -lupinine
5. Synthesis of (.+-.)-kopsanone and (.+-.)-10,22-dioxokopsane, hetacyclic indole alkaloids
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2. Preparation of Difunctional Compounds;Compendium of Organic Synthetic Methods;2006-11-22
3. Stereoselectivities of the intramolecular Diels-Alder reaction in the azanona- and azadecatriene series. Preparation of some polyhydroisoindoles, polyhydroisoquinolines, decahydropyrido[2,1-a]isoindoles and decahydro-2H-pyrido[1,2-b]isoquinolines;Tetrahedron;1998-08
4. A New Benzoylglucoside and a New Prenylated Isoflavone from Lophira lanceolata;Journal of Natural Products;1998-05-12
5. Synthesis of nitrogen heterocycles from vinyl glycine derivatives via palladium catalysis;Tetrahedron Letters;1994-12
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