An Efficient Deprotective Method for Allylic Alcohols Protected as Methoxyethoxymethyl (MEM) And Methoxymethyl (MOM) Ethers
- 1 October 1983
- journal article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 13 (12) , 1021-1026
- https://doi.org/10.1080/00397918308082721
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- A total synthesis of lasalocid AJournal of the American Chemical Society, 1978
- Total synthesis of (.+-.)-vernolepinJournal of the American Chemical Society, 1978
- Shikimate-derived metabolites. Total synthesis of nor-chorismic acidJournal of the Chemical Society, Chemical Communications, 1978
- Pyridinium p-toluenesulfonate. A mild and efficient catalyst for the tetrahydropyranylation of alcoholsThe Journal of Organic Chemistry, 1977
- Chiral synthesis of prostaglandins (PGE1) from D-glyceraldehydeJournal of the American Chemical Society, 1977
- A new general method for protection of the hydroxyl functionTetrahedron Letters, 1976
- 2-Thiazolines in organic synthesis. Formation of .beta.-hydroxy aldehydes with protected hydroxy groups. Synthesis of homoallylic alcoholsThe Journal of Organic Chemistry, 1975
- An Improved Method for Methoxymethylation of Alcohols under Mild Acidic ConditionsSynthesis, 1975
- Synthesis of terrein, a metabolite of Aspergillus terreusJournal of the Chemical Society, Chemical Communications, 1974
- Prostaglandins. X. Synthesis of prostaglandin models and prostaglandins by conjugage addition of a functionalized organocopper reagentJournal of the American Chemical Society, 1972