The synthesis of indolizidines by intramolecular ene cyclizations. Preparation of (E)-alkylidene analogs of pumiliotoxin A.
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[1] B. Snider,et al. Intramolecular and intermolecular Lewis acid catalyzed ene reactions using ketones as enophiles , 1984 .
[2] L. Overman,et al. Enantioselective total synthesis of allopumiliotoxin A alkaloids 267A and 339B , 1984 .
[3] L. Overman,et al. Enantioselective total syntheses of pumiliotoxin B and pumiliotoxin 251D. A general entry to the pumiliotoxin A alkaloids via stereospecific iminium ion-vinylsilane cyclizations , 1984 .
[4] W. Oppolzer,et al. Stereospecific, R2AlCl‐Promoted Intramolecular Ene Reaction of a 1,6‐Dienoate: Evidence for a Concerted Mechanism , 1984 .
[5] J. Daly,et al. pumiliotoxins: magnetic resonance spectral assignments and structural definition of pumiliotoxins A and B and related allopumiliotoxins , 1984 .
[6] L. Overman,et al. Enantiospecific total synthesis of dendrobatid toxin 251D. A short chiral entry to the cardiac-active pumiliotoxin A alkaloids via stereospecific iminium ion-vinylsilane cyclizations , 1981 .
[7] B. Snider,et al. Lewis-acid catalyzed ene reactions , 1980 .
[8] Victor Snieckus,et al. Intramolecular Ene Reactions in Organic Synthesis , 1978 .
[9] P. Mccurry,et al. Synthesis of spiro-sesquiterpenes in the vetivane series via an aza-claisen rearrangement , 1973 .
[10] N. Andersen,et al. Stereochemical course of the cyclization of olefinic aldehydes , 1972 .
[11] H. Hoffmann. The Ene Reaction , 1969 .