Total synthesis of (+)-pederin. 2. Stereocontrolled synthesis of (+)-benzoylselenopederic acid and total synthesis of (+)-pederin
- 31 December 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (52), 6465-6468
- https://doi.org/10.1016/s0040-4039(00)99028-2
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Asymmetric acylation of carboxamides havingTetrahedron Letters, 1984
- An introduction of chiral centers into acyclic systems based on stereoselective ketone reductionAccounts of Chemical Research, 1984
- Asymmetric acylation reactions of chiral imide enolates. The first direct approach to the construction of chiral .beta.-dicarbonyl synthonsJournal of the American Chemical Society, 1984
- A new stereocontrolled synthesis of (+)-pederine. Unusual conformation around c-10—c-11 bond in pederine derivativesTetrahedron Letters, 1983
- Total synthesis of (.+-.)-pederamideJournal of the American Chemical Society, 1979
- Synthetic studies toward mitomycins. 1. Total synthesis of deiminomitomycin AJournal of the American Chemical Society, 1977
- Organoselenium chemistry. A facile one-step synthesis of alkyl aryl selenides from alcoholsThe Journal of Organic Chemistry, 1976
- New method for the conversion of nitro groups into carbonylsThe Journal of Organic Chemistry, 1973