We describe a biomimetic organocatalytic enantioselective decarboxylative addition of
malonic acid half thioesters to imines. This simple protocol makes use of readily available …

Catalytic decarboxylative reactions are attractive as biomimetic and environmentally friendly
reaction processes. This review summarizes the recent results of organocatalytic …

Catalytic decarboxylative reactions are attractive as biomimetic reactions and
environmentally friendly reaction processes. In this review, the origin and recent …

BJOC - Asymmetric organocatalytic decarboxylative Mannich reaction using β-keto acids: A
new protocol for the synthesis of chiral β-amino ketones Journal Logo Diamond Open Access …

The organocatalytic enantioselective decarboxylative Mannich reaction of malonic acid half
thioesters (MAHTs) with cyclic N‐sulfonyl ketimines by using N‐heteroarenesulfonyl …

An organocatalytic asymmetric decarboxylative amination reaction of β-keto acids is
described. Under mild reaction conditions, a series of chiral α-amino ketones were obtained …

The methodology of enantioselective decarboxylation was applied to 2‐aminomalonic acid
derivatives in order to obtain enantio‐enriched amino acid derivatives. Full conversion was …

The organocatalytic enantioselective decarboxylative addition of malonic acids half
thioesters to isatins using a squaramide catalyst afforded the products with high …

Thiourea derived cinchona alkaloids promote the asymmetric decarboxylative protonation of
cyclic, acyclic, or bicyclic α-aminomalonate hemiesters under mild and metal-free conditions …

An asymmetric Mannich reaction of phenylacetate thioesters and sulfonylimines using
cinchona alkaloid-based amino (thio) urea catalysts is reported that employs proximity …