| Literature DB >> 30275612 |
Shahien Shahsavari1, Travis Wigstrom1, James Gooding1, Chase McNamara1, Shiyue Fang1.
Abstract
The 1,3-dithian-2-yl-methyl (Dim) and its analogous groups including dimethyl-Dim (dM-Dim) can provide a new dimension of orthogonality for carboxylic acid protection. They can be deprotected under nearly neutral oxidative conditions. In this paper, the protection of carboxylic acid with dM-Dim, deprotection of dM-Dim ester with sodium periodate, stability of dM-Dim protected carboxylic acid under acidic and basic conditions, and selective deprotection of dM-Dim protected carboxylic acids in the presence of tertiary butyl and methyl esters are presented.Entities:
Keywords: carboxylic acid; dM-Dim; oxidation; protecting group
Year: 2018 PMID: 30275612 PMCID: PMC6161831 DOI: 10.1016/j.tetlet.2018.03.076
Source DB: PubMed Journal: Tetrahedron Lett ISSN: 0040-4039 Impact factor: 2.415