Biocatalytic resolutions of sulfinylalkanoates: a facile route to optically active sulfoxides
摘要:
Two methods are presented for kinetic resolutions of compounds containing ester and sulfoxide functionalities (sulfinylalkanoates). In the first a crude lipase preparation from Pseudomonas sp. (K10) mediates enantioselective hydrolysis of these esters in an aqueous environment. The second method uses the same lipase preparation to promote enantioselective transesterifications with alcohols in hexane. Both procedures are suitable for preparation of sulfinylalkanoates where the ester and sulfoxide groups are separated by one or two methylene units (sulfinylacetates and sulfinylpropanoates) but compounds with three methylene "spacer groups" (sulfinylbutanoates) are not substrates for the lipase under either set of conditions.
Biocatalytic resolutions of methyl sulfinylacetates fford sulfoxides (R)-(1) - (6) in very high optical yields; the products have been used in a systematic study of the “SPAC” reaction, an asymmetric synthesis of γ-hydroxy-α,β-unsaturated esters.
Stereochemically matched sulfinylacetates for double diastereoselection in the spac reaction
作者:Kevin Burgess、Ian Henderson
DOI:10.1016/s0040-4020(01)82313-9
日期:1991.8
which the sulfoxide asymmetry is matched with the inducing effect of the auxiliary give good diastereoselection in SPAC reactions affording γ-hydroxy-α,β-unsaturatod alcohols of high optical purity. Asymmetry at the sulfoxide has a greater effect than the auxiliaries on the stereochemical outcome of these reactions.
Biocatalytic resolutions of sulfinylalkanoates: a facile route to optically active sulfoxides
作者:Kevin Burgess、Ian Henderson、Kwok Kan Ho
DOI:10.1021/jo00030a044
日期:1992.2
Two methods are presented for kinetic resolutions of compounds containing ester and sulfoxide functionalities (sulfinylalkanoates). In the first a crude lipase preparation from Pseudomonas sp. (K10) mediates enantioselective hydrolysis of these esters in an aqueous environment. The second method uses the same lipase preparation to promote enantioselective transesterifications with alcohols in hexane. Both procedures are suitable for preparation of sulfinylalkanoates where the ester and sulfoxide groups are separated by one or two methylene units (sulfinylacetates and sulfinylpropanoates) but compounds with three methylene "spacer groups" (sulfinylbutanoates) are not substrates for the lipase under either set of conditions.
Enzymatic Resolution and Decarboxylative Functionalization of α‐Sulfinyl Esters
作者:Suraksha Gahalawat、Yesu Addepalli、Stephen P. Fink、Lakshmi Kasturi、Sanford D. Markowitz、Joseph M. Ready
DOI:10.1002/chem.202302996
日期:2024.2
Enzymaticresolution of α-sulfinyl esters gives recovered ester and α-sulfinyl acid in high enantiomeric purity. Decarboxylative functionalization provides access to a wide range of optically active sulfoxides in both enantiomeric forms.