Paper
(1-nosyl-5-nitroindol-3-yl)methyl ester: a novel protective group for carboxylic acids.
Published May 17, 2008 · T. Nishimura, Kouhei Yamada, Tohru Takebe
Organic letters
12
Citations
0
Influential Citations
Abstract
The usefulness of (1-nosyl-5-nitroindol-3-yl)methyl esters as a novel protective group for carboxylic acid is fully demonstrated. The novel protective group is stable under a broad range of conditions and can easily be deprotected under the mild conditions used for removal of the nosyl (Ns) group. It is orthogonal to the existing protective groups for carboxylic acids such as t-butyl and allyl esters.
(1-nosyl-5-nitroindol-3-yl)methyl esters are a stable, easy-to-deprotect protective group for carboxylic acids, offering a promising alternative to existing protective groups like t-butyl and allyl esters.
Full text analysis coming soon...