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- W1979808415 abstract "Condensation of 2-acetyl benzoic acid with l-cysteine esters proceeds with extremely high diastereoselectivity to produce the desired thiazolo[2,3-a]isoindolin-1-one products in good yield. The relative stereochemistry of the major diastereoisomer has been determined by X-ray crystallography. Stereoselective enolate alkylation of this substrate has been investigated as a method to manipulate the ring skeleton, and was found to proceed with up to exclusive levels of stereoselectivity." @default.
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- W1979808415 date "2000-03-01" @default.
- W1979808415 modified "2023-09-27" @default.
- W1979808415 title "Highly diastereoselective synthesis and template manipulation of the thiazolo[2,3-a]isoindolin-1-one ring system" @default.
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- W1979808415 doi "https://doi.org/10.1016/s0040-4039(00)00128-3" @default.
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