β-Lactams from tetrahydro-1,2-oxazine-3,6-diones, and a labelling study of the product stereochemistry
摘要:
The stereochemistry of the N-C bond-forming step in the photochemical conversion of a tetrahydro-1,2-oxazine-3,6-dione to a beta-lactam has been shown to rake place with scrambling of stereochemistry using a deuterium labelled precursor.
β-Lactams from tetrahydro-1,2-oxazine-3,6-diones, and a labelling study of the product stereochemistry
摘要:
The stereochemistry of the N-C bond-forming step in the photochemical conversion of a tetrahydro-1,2-oxazine-3,6-dione to a beta-lactam has been shown to rake place with scrambling of stereochemistry using a deuterium labelled precursor.
The stereochemistry of the N-C bond-forming step in the photochemical conversion of a tetrahydro-1,2-oxazine-3,6-dione to a beta-lactam has been shown to rake place with scrambling of stereochemistry using a deuterium labelled precursor.