Trimethylsilyl Esters: Temporary Protection of Carboxylic Acids During Hydroboration Reactions
- 1 September 1989
- journal article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 19 (16), 2783-2787
- https://doi.org/10.1080/00397918908052665
Abstract
Carboxylic acid are readily protected during hydroboration reactions by converting them to the corresponding trimethylsilyl esters.Keywords
This publication has 5 references indexed in Scilit:
- Trimethylsilyl esters: protection of carboxylic acids during hydroboration reactionsOrganometallics, 1989
- 1,3,2-Benzodioxaborole in Organic Synthesis: Preparation of Vinyl lodidesHETEROCYCLES, 1982
- Syntheses of organic iodides via reaction of organoboranes with sodium iodideThe Journal of Organic Chemistry, 1981
- A Convenient Procedure for the Syntheses of Vinyl Iodides via the Reaction of Iodine Monochloride with Vinylboronic AcidsSynthetic Communications, 1981
- Sur les acides‐alcools polyméthylène‐carboniques de 8 à 21 atomes de carboneHelvetica Chimica Acta, 1929