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• W2912784770 abstract "A highly efficient catalytic enantioselective [4+2] cycloaddition was developed between 2-benzothiazolimines and enecarbamates. A wide range of benzothiazolopyrimidines bearing three contiguous stereogenic centers was obtained in high to excellent yields and with excellent diastereo- and enantioselectivities (d.r. > 98 : 2 and up to >99% ee). Furthermore, this chiral phosphoric acid-catalyzed strategy was scalable and enabled access to a new class of optically pure Lewis base isothiourea derivatives." @default.
• W2912784770 created "2019-02-21" @default.
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• W2912784770 date "2019-01-01" @default.
• W2912784770 modified "2023-10-18" @default.
• W2912784770 title "Chiral phosphoric acid-catalyzed enantioselective construction of structurally diverse benzothiazolopyrimidines" @default.
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• W2912784770 doi "https://doi.org/10.1039/c8sc05581e" @default.
• W2912784770 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6461124" @default.
• W2912784770 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31015920" @default.
• W2912784770 hasPublicationYear "2019" @default.
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