Skip to Content
Merck
  • A bidirectional synthesis of spiroacetals via Rh(ii)-catalysed C-H insertion.

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

Chemical communications (Cambridge, England) (2017-03-31)
Romain J Lepage, Jonathan M White, Mark J Coster
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%).

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Rh2(S-PTAD)4