Direct enantioselective vinylogous Mannich-type reactions of acyclic enals: New experimental insights into the E/Z-dilemma.

Direct enantioselective vinylogous Mannich-type reactions of acyclic enals: New experimental insights into the E/Z-dilemma.
Chirality. 2019 May 15;:
Authors: Vargiu M, Favero L, Menichetti A, Di Bussolo V, Marchetti F, Pescitelli G, Di Pietro S, Pineschi M
Abstract
The direct heterofunctionalization of acyclic α,β-unsaturated aldehydes with N-acylquinolinium ions contemplating the formation of two stereocentres is studied using dienamine catalysis. This work gives some new experimental insights on the remote stereocontrol in dienamine catalysis using unbiased aliphatic systems and large electrophiles, pointing to a (Z)-preference of the reactive configuration of the second double bond.
PMID: 31090981 [PubMed - as supplied by publisher]

Source: Chirality - May 14, 2019 Category: Molecular Biology Authors: Vargiu M, Favero L, Menichetti A, Di Bussolo V, Marchetti F, Pescitelli G, Di Pietro S, Pineschi M Tags: Chirality Source Type: research