A route to Prelog-Djerassi lactone from methyl α,D-glucopyranoside
- 31 December 1981
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 22 (27) , 2533-2534
- https://doi.org/10.1016/s0040-4039(01)90512-x
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- The synthesis of chiral subunits for macrolide synthesis: the Prelog-Djerassi lactone and derivativesThe Journal of Organic Chemistry, 1981
- Geminal acylation-alkylation at a carbonyl carbon via regiospecifically generated metalloenaminesJournal of the American Chemical Society, 1980
- Highly Stereoselective Aldol Condensation Using an Enantioselective Chiral EnolateAngewandte Chemie International Edition in English, 1980
- A stereoselective total synthesis of the Prelog-Djerassi lactoneJournal of the American Chemical Society, 1980
- Macrolide antibiotics. 1. Total synthesis of the Prelog-Djerassi lactone and methynolideJournal of the American Chemical Society, 1979
- A stereocontrolled synthesis of the (.+-.) Djerassi-Prelog lactonic acidJournal of the American Chemical Society, 1979
- Dehydrohalogenation by complex base. Preferential loss of "poorer" halogen leaving groupsJournal of the American Chemical Society, 1979
- Syntheses of macrolide antibiotics. I. MethymycinJournal of the American Chemical Society, 1975
- A NEW ALDEHYDE SYNTHESISJournal of the American Chemical Society, 1958
- The Structure of the Antibiotic Methymycin1Journal of the American Chemical Society, 1956