Synthesis via sigmatropic rearrangements. 10. Synthesis of 2,3-disubstituted indoles via Claisen ortho ester rearrangement. An approach for the synthesis of vindorosine
- 1 January 1986
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 51 (2) , 123-130
- https://doi.org/10.1021/jo00352a001
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- Synthesis of the Antitumor Dimeric Indole Alkaloids From Catharanthus Species (Vinblastine Group)Journal of Natural Products, 1980
- Dihydropyridines in synthesis and biosynthesis. I. Secodine and precursors of dehydrosecodineCanadian Journal of Chemistry, 1979
- Total synthesis of indole and dihydroindole alkaloids. 14. A total synthesis of vindolineJournal of the American Chemical Society, 1978