Hydroformylation as a simple and efficient one carbon homologation of homoallylic alcohols. Synthesis of prelog-djerassi lactone.
- 31 December 1984
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 25 (37) , 4051-4054
- https://doi.org/10.1016/s0040-4039(01)90179-0
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Stereoselektive Synthese von Alkoholen, XI. Doppelte Stereodifferenzierung bei der Addition von Crotylboronsäureestern an Aldehyde: Prelog‐Djerassi ‐LactonEuropean Journal of Inorganic Chemistry, 1982
- Synthesis of racemic Prelog-Djerassi lactone via a regio- and diastereoselective ene reactionThe Journal of Organic Chemistry, 1982
- Stereochemical consequences of the Lewis acid catalyzed cyclocondensation of oxygenated dienes with aldehydes. A rapid and stereoselective entry to various natural products derived from propionateJournal of the American Chemical Society, 1982
- Total synthesis of 6-deoxyerythronolide BJournal of the American Chemical Society, 1981
- The synthesis of chiral subunits for macrolide synthesis: the Prelog-Djerassi lactone and derivativesThe Journal of Organic Chemistry, 1981
- 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
- TOTAL SYNTHESIS OF METHYNOLIDE: SYNTHESIS OF TWO INTERMEDIATES, 3,4-DIACETOXY-3-METHYL-1-HEXYNE AND PRELOG-DJERASSI LACTONIC ACIDChemistry Letters, 1979
- Macrolide antibiotics. 1. Total synthesis of the Prelog-Djerassi lactone and methynolideJournal of the American Chemical Society, 1979
- Dehydrohalogenation by complex base. Preferential loss of "poorer" halogen leaving groupsJournal of the American Chemical Society, 1979