Studies on the Asymmetric Synthesis of Stemona Alkaloids: Total Synthesis of (−)‐Stenine
- 3 May 1996
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 35 (8) , 904-906
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Asymmetric Total Synthesis of the Stemona Alkaloid (-)-StenineJournal of the American Chemical Society, 1995
- Asymmetric synthesis of either enantiomer of opium alkaloids and morphinans. Total synthesis of (-)- and (+)-dihydrocodeinone and (-)- and (+)-morphineJournal of the American Chemical Society, 1993
- A Diels-Alder approach to Stemona alkaloids: total synthesis of stenineThe Journal of Organic Chemistry, 1993
- A Modified Synthesis of (+-)-(E)-7-Methyl-1,6-dioxaspiro[4,5]decane.Acta Chemica Scandinavica, 1993
- Synthetic Studies on the Stemona Alkaloids; Stereochemical Course of PhSe+-Induced Seven-Membered Ring FormationSynlett, 1990
- Studies of Stemona alkaloids. Total synthesis of (+)-croomineJournal of the American Chemical Society, 1989
- Asymmetric Diels‐Alder and Ene Reactions in Organic Synthesis. New Synthetic Methods (48)Angewandte Chemie International Edition, 1984
- Diphenylphosphoryl azide. New convenient reagent for a modified Curtius reaction and for peptide synthesisJournal of the American Chemical Society, 1972
- The Structure of Stenine, a New Alkaloid Occurring in Stemona TuberosaChemical and Pharmaceutical Bulletin, 1967
- The stereochemistry and absolute configuration of stenine and tuberostemonineChemical Communications (London), 1967