Catalytic asymmetric synthesis of geminal-dicarboxylates. Issue 29 (5th July 2018)

• Record Type: Journal Article
• Authors: Mistry, Nisha; Fletcher, Stephen P.
• Is Part Of: Chemical science. Volume 9:Issue 29(2018)
• Page Start: 6307
• Page End: 6312
• Publication Date: 2018-07-05
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c8sc01786g
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : Here we report a rhodium-catalyzed asymmetric carboxylation of ester-containing allylic bromides to form stereogenic carbon centers bearing two different carboxylates with high yields and enantioselectivities. Abstract : Stereogenic acetals, spiroacetals and ketals are well-studied stereochemical features that bear two heteroatoms at a common carbon atom. These stereocenters are normally found in cyclic structures while linear (or acyclic) analogues bearing two heteroatoms are rare. Chiral geminal-dicarboxylates are illustrative, there is no current way to access this class of compounds while controlling the stereochemistry at the carbon center bound to two oxygen atoms. Here we report a rhodium-catalysed asymmetric carboxylation of ester-containing allylic bromides to form stereogenic carbon centers bearing two different carboxylates with high yields and enantioselectivities. The products, which are surprisingly stable to a variety of acidic and basic conditions, can be manipulated with no loss of enantiomeric purity as demonstrated by ring closing metathesis reactions to form chiral lactones, which have been extensively used as building blocks in asymmetric synthesis.