A short synthesis of (±)-alloyohimbane via a thioisomünchnone based intramolecular dipolar-cycloaddition reaction
Authors:
- Todd M. HeidelbaughTHTodd M. Heidelbaugh
- Bing LiuBLBing Liu
- Albert PadwaAPAlbert Padwa
- 1 July 1998
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 39 (27) , 4757-4760
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Construction of tetracyclic indole bases via Aza Diels‐Alder reaction of indolylethylimines with Brassard's dieneEuropean Journal of Organic Chemistry, 1994
- Asymmetric synthesis of indolo[2,3-a]quinolizidin-2-ones - congeners to yohimbine-type alkaloidsTetrahedron, 1993
- Total syntheses of yohimbe alkaloids, with stereoselection for the normal, allo, and 3-epiallo series, based on annelations of 4-methoxy-1,2-dihydropyridonesThe Journal of Organic Chemistry, 1991
- Formal total synthesis of deserpidine demonstrating a versatile amino-Claisen rearrangement/Wenkert cyclization strategy for the preparation of functionalized yohimbane ring systemsJournal of the American Chemical Society, 1990
- Indole alkaloids in human medicinePure and Applied Chemistry, 1990
- The stereospecific synthesis of reserpinePure and Applied Chemistry, 1989
- General strategies for the synthesis of indole alkaloids. Total synthesis of (.+-.)-reserpine and (.+-.)-.alpha.-yohimbineJournal of the American Chemical Society, 1987
- General Methodology for cis-Hydroisoquinoline Synthesis. 3. A Sixteen Step Synthesis of ReserpineHETEROCYCLES, 1987
- Total synthesis of (.+-.)-reserpineJournal of the American Chemical Society, 1985
- General methodology for cis-hydroisoquinoline synthesis: synthesis of reserpineJournal of the American Chemical Society, 1980