Synthetic studies on paraherquamide: Regioselectivity of indole oxidation
- 31 December 1989
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 30 (41) , 5575-5578
- https://doi.org/10.1016/s0040-4039(01)93803-1
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Chemical modification of paraherquamide. 1. Unusual reactions and absolute stereochemistryThe Journal of Organic Chemistry, 1989
- Remarkable, enantio-divergent biogenesis of brevianamide A and BJournal of the American Chemical Society, 1989
- Studies in the Formation of Oxidoles from Their Indolozabicyclo[3.3.1]nonane Counterparts and Implications for the Biogenesis of AlstonisineHETEROCYCLES, 1989
- Facial selectivity of the intramolecular SN2' cyclization: stereocontrolled total synthesis of brevianamide BJournal of the American Chemical Society, 1988
- Promising cyclization reactions to construct the ring systems of brevianamides A,BTetrahedron Letters, 1986
- Structures of marcfortine B and C (X-ray analysis), alkaloids fromTetrahedron Letters, 1981
- The structure of paraherquamide, a toxic metabolite fromTetrahedron Letters, 1981
- Isolation and structure (X-ray analysis) of marcfortine A, a new alkaloid from Penicillium roquefortiJournal of the Chemical Society, Chemical Communications, 1980