2001
Heraclio López-Ruiz y S. Z. Zard. A flexible Access to Highly Functionalised Boronates. Chem. Commun. 2618-2619 (2001) DOI: 10.1039/B109637K
Abstract
The radical addition of various xanthates to allyl or vinyl boronates occurs smoothly in the presence of a small amount of lauroyl peroxide as initiator to give good yields of usefully functionalised boronates.
Diastereoselective Synthesis of Spiro-?-lactams via Staudinger Reaction
Diastereoselective alkylation of chiral glycinate derivatives containing the ?-phenylethyl group.
Diastereoselective alkylation of chiral glycinate derivatives containing the ?-phenylethyl group.
A practical access to acyl radicals from acyl hydrazides
A flexible access to highly functionalised boronates
Stereoselective addition of allylmagnesium chloride to the CN bond of [4.3.0] boron heterobicycles
Preparation of N-aryl-substituted spiro-?-lactams via Staudinger cycloaddition
Stereoselective addition of allylmagnesium chloride to the CN bond of [4.3.0] boron heterobicycles