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- W2949551384 abstract "Highly atroposelective Meyers’ lactamization promoted by pivalic acid under microwave irradiation is reported which allows the construction of nonracemic substituted-dibenzo(di)azepine derivatives through a center to axial chirality transfer principle, controlling the otherwise configurationally labile biaryl axis. This approach provides a straightforward entry to enantioenriched analogues of biorelevant architectures." @default.
- W2949551384 created "2019-06-27" @default.
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- W2949551384 date "2013-08-07" @default.
- W2949551384 modified "2023-10-16" @default.
- W2949551384 title "Developments in Meyers’ Lactamization Methodology: En Route to Bi(hetero)aryl Structures with Defined Axial Chirality" @default.
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- W2949551384 doi "https://doi.org/10.1021/jo401259w" @default.
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