Truong, Ngoc published the artcileDirect carbon-carbon bond formation via reductive soft enolization: a syn-selective Mannich addition of ¦Á-iodo thioesters, Category: catalysis-chemistry, the publication is Organic & Biomolecular Chemistry (2016), 14(33), 7864-7868, database is CAplus and MEDLINE.
The ¦Â-amino carboxylic acid moiety is a key feature of numerous important biol. active compounds We describe a syn-selective direct Mannich addition reaction that uses ¦Á-iodo thioesters and sulfonyl imines and produces ¦Â-amino thioesters. Enolate formation is achieved by reductive soft enolization. The products of the reaction provide straightforward access to biol. important ¦Â-lactams through a variety of known reactions.
Organic & Biomolecular Chemistry published new progress about 22693-41-0. 22693-41-0 belongs to catalysis-chemistry, auxiliary class Other Functionalization Reagent, name is 2,4,6-Triisopropylbenzenethiol, and the molecular formula is C7H10O4, Category: catalysis-chemistry.
Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia