A bidirectional synthesis of spiroacetals via Rh(ii)-catalysed C-H insertion

Chem Commun (Camb). 2017 Apr 11;53(30):4219-4221. doi: 10.1039/c7cc00459a.

Abstract

Acyclic methylene acetals bearing two diazoester subunits have been converted to [5,5]-spiroacetals via bidirectional C-H insertion under Rh(ii) catalysis. Using a chiral Rh(ii) catalyst, the major diastereomer can be produced in high enantiomeric excess (89%).