Studies on the asymmetric total synthesis of trichothecenes. Stereoselective construction of the c-ring fragment
- 31 December 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (32) , 3765-3768
- https://doi.org/10.1016/s0040-4039(00)89245-x
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- The diastereospecific aprotic conjugate addition reactions of carbanions derived from allylic sulfoxides and allylic phosphine oxides.Tetrahedron Letters, 1985
- Asymmetric synthesis via chiral sulfinylallyl anion. Total synthesis of (+)-hirsutene: facile ring closure involving enol thioether and enol acetate moietiesJournal of the American Chemical Society, 1985
- The diastereospecific aprotic conjugate addition reactions of allylic anions-mechanistic aspects.Tetrahedron Letters, 1985
- Total synthesis of the trichothecene mycotoxin anguidineJournal of the American Chemical Society, 1983
- Macrocyclic and other novel trichothecenes: their structure, synthesis, and biological significanceAccounts of Chemical Research, 1982
- Synthetic studies of trichothecenes, an enantioselective synthesis of a C-ring precursor of anguidineTetrahedron Letters, 1982
- Thallium nitrate as a reagent for the conversion of epoxides into α-hydroxynitrate esters and for the cleavage of aliphatic ethersTetrahedron Letters, 1980
- D-Moenuronsäure (4-C-methyl-D-glucoronsäure), ein neuer baustein des antibiotikums moenomycin A.Tetrahedron Letters, 1978
- Simple total synthesis of prostaglandins from 4-cumyloxy-2-cyclopentenoneJournal of the American Chemical Society, 1975
- Pyridinium chlorochromate. An efficient reagent for oxidation of primary and secondary alcohols to carbonyl compoundsTetrahedron Letters, 1975