Enantiospecific and diastereoselective synthesis of C11-C17 fragment of tylonolide from “asymmetrized tris (hydroxymethyl)methane”
- 7 January 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (2) , 267-270
- https://doi.org/10.1016/0040-4039(91)80872-4
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Asymmetrized trils (hydroxymethyl)methane as a highly stereodivergent chiral building block: preparation of all four stereoisomers of protected 2-hydroxymethyl-1,3-butanediolTetrahedron Letters, 1990
- Stereocontrolled functionalization of cycloheptadiene using organometallic chemistry: synthesis of the (+)-Prelog-Djerassi lactone and a tylosin subunitThe Journal of Organic Chemistry, 1989
- Enzymes as selective reagents in organic synthesis: Enantioselective preparation of “asymmetrized tris (hydroxymethyl)methane”Tetrahedron Letters, 1989
- STEREOCONTROLLED SYNTHESIS OF SEGMENTS FOR THE SYNTHESIS OF TYLONOLIDE BY USING A RELATIVE 1,2-ASYMMETRIC INDUCTIONChemistry Letters, 1986
- Total synthesis of tylonolide, the aglycone of the 16-membered ring macrolide tylosin, from D-glucose. Selective application of MPM and DMPM protecting groups for hydroxy functionsTetrahedron Letters, 1986
- Synthesis of tylonolide, the aglycone of tylosinJournal of the American Chemical Society, 1982
- Bicyclo[2.2.1]heptanes in organic synthesis. Total synthesis of the 16-membered ring macrolide tylonolide hemiacetal: synthesis and coupling of the C(3)-C(9) and C(11)-C(17) fragmentsJournal of the American Chemical Society, 1982
- Aldol methodology: synthesis of versatile intermediates, 3-hydroxy-2-vinylcarbonyl compoundsJournal of the American Chemical Society, 1982
- Carbohydrates in organic synthesis. Synthesis of 16-membered-ring macrolide antibiotics. 5. Total synthesis of O-mycinosyltylonolide: synthesis of key intermediatesJournal of the American Chemical Society, 1982
- Total synthesis of tylonolide, an aglycone of tylosinTetrahedron Letters, 1981