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- W2097735384 abstract "Highly diastereoselective reductions and organometallic additions in bicyclic lactams have been observed, which appear to result either from a stereoelectronic interaction of the pyramidalised nitrogen lone pair or from steric interactions in the bicyclic system. These products can be readily deprotected to give hydroxylated lactams." @default.
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- W2097735384 date "2001-12-05" @default.
- W2097735384 modified "2023-09-27" @default.
- W2097735384 title "Diastereocontrolled synthesis of hydroxylated lactams" @default.
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- W2097735384 doi "https://doi.org/10.1039/b108056n" @default.
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