Abstract
A novel catalytic asymmetric P-C bond formation between phosphinates/phosphine oxide and allylic carbonates was developed. This methodology could not only afford a variety of functionalized adjacent P,C-stereogenic phosphorus compounds in high yields with high regio- and diastereoselectivities but also provide an alternative strategy to access enantiomerically enriched (SP)-phosphinates through kinetic resolution. New strategy for adjacent P,C-stereogenic phosphorus compounds: A novel catalytic asymmetric P-C bond formation between phosphinates/phosphine oxide and allylic carbonates was developed. This methodology could not only afford a variety of functionalized adjacent P,C-stereogenic phosphorus compounds in high yields with high regio- and diastereoselectivities but also provide an alternative strategy to access enantiomerically enriched (SP)-phosphinates through kinetic resolution.
Original language | English |
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Pages (from-to) | 1353-1356 |
Number of pages | 4 |
Journal | Chemistry - An Asian Journal |
Volume | 11 |
Issue number | 9 |
DOIs | |
State | Published - 6 May 2016 |
Keywords
- 1,3-bisphosphinylpropanes
- P-C bond formation
- P-stereogenic compounds
- kinetic resolution
- organocatalysis