Regioselective and stereoselective reductive cleavage of 1,7-dioxaspiro[5.5]undecane alcohols
- 5 August 1996
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 37 (32) , 5649-5652
- https://doi.org/10.1016/0040-4039(96)01196-3
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Total Synthesis of the Antiparasitic Agent Avermectin B1aJournal of the American Chemical Society, 1995
- Total synthesis of the macrolide antibiotic rutamycin BJournal of the American Chemical Society, 1993
- Bioactive marine metabolites. 48. Cinachyrolide A: a potent cytotoxic macrolide possessing two spiro ketals from marine sponge Cinachyra spJournal of the American Chemical Society, 1993
- Antineoplastic agents. 257. Isolation and structure of spongistatin 1The Journal of Organic Chemistry, 1993
- Total synthesis of the macrolide antibiotic cytovaricinJournal of the American Chemical Society, 1990
- Chemistry of spiroketalsChemical Reviews, 1989
- A synthesis of (-)-talaromycin AThe Journal of Organic Chemistry, 1989
- Diastereotopic selectivity at prochiral carbon centers: functionalization of differentiated hydroxymethyl groups provides access to either stereoisomeric configurationJournal of the American Chemical Society, 1985
- Macrolide total synthesis. The synthesis of seco-acid derivatives for the synthesis of methymycin and 10-deoxymethymycinThe Journal of Organic Chemistry, 1983
- Macrolide total synthesis. The synthesis of spiro ketal intermediates and their cleavage into open-chain derivativesThe Journal of Organic Chemistry, 1983