Synthetic studies on pyrrolizidine alkaloids. II. Intramolecular additions of radicals and electrophiles to allylstannanes as methods for ring closure
Authors:
- Gary E. KeckGKGary E. Keck
- Eric J. EnholmEEEric J. Enholm
- 1 January 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (28) , 3311-3314
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- .alpha.-Acylamino radical cyclizations: syntheses of isoretronecanolJournal of the American Chemical Society, 1984
- Pyrrolizidinone and indolizidinone synthesis: generation and intramolecular addition of .alpha.-acylamino radicals to olefins and allenesJournal of the American Chemical Society, 1984
- Total syntheses of dl-gephyrotoxin and dl-dihydrogephyrotoxinJournal of the American Chemical Society, 1983
- New methods for alkaloid synthesis: .alpha.-acylamino radical cyclizationsJournal of the American Chemical Society, 1982
- Stereospecific synthesis of retronecine by imidate methylide cycloadditionJournal of the American Chemical Society, 1980
- Desulfurizative stannylation of propargylic or allylic sulfides via an SH' processJournal of the American Chemical Society, 1979
- Stereochemistry, conformational analysis, and transannular cyclizations of nine-membered ring azaolefinsThe Journal of Organic Chemistry, 1979
- The chemistry of azocines. Intermediates for the synthesis of pyrrolizidinesThe Journal of Organic Chemistry, 1977
- Kinetically controlled total syntheses of dl-trachelanthamidine and dl-isoretronecanolJournal of the American Chemical Society, 1977
- A new synthesis of the pyrrolizidine alkaloids (.+-.)-isoretronecanol and (.+-.)-trachelanthamidineThe Journal of Organic Chemistry, 1977