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- W2949556660 abstract "Conjugate additions of alkyl-1-methyl-2-imidazolyl and 2-pyridyl sulfoxides to α,β-unsaturated esters proceeded in high yield and with excellent diastereoselectivity when LHMDS, rather than LDA, was used as the base. Additions to enones were complicated by competitive 1,2-addition. A benzyl imidazolyl sulfoxide underwent selective conjugate addition to an enone, but did not react with unsaturated esters. In contrast, a benzyl 2,4-dimethoxyphenyl sulfoxide gave high yields and stereoselectivity in additions to unsaturated esters." @default.
- W2949556660 created "2019-06-27" @default.
- W2949556660 date "2000-01-01" @default.
- W2949556660 modified "2023-10-01" @default.
- W2949556660 title "Highly Stereoselective Conjugate Additions of Heteroaryl Alkyl Sulfoxides" @default.
- W2949556660 doi "https://doi.org/10.1055/s-2000-8691" @default.
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