Stereospecific Nucleophilic Substitution with Arylboronic Acids as Nucleophiles in the Presence of a CONH Group.
- Resource Type
- Article
- Authors
- Tian, Duanshuai; Li, Chengxi; Gu, Guoxian; Peng, Henian; Zhang, Xumu; Tang, Wenjun
- Source
- Angewandte Chemie. 6/11/2018, Vol. 130 Issue 24, p7294-7298. 5p.
- Subject
- *NUCLEOPHILIC substitution reactions
*STEREOSPECIFICITY
*BORONIC acids
*COUPLING reactions (Chemistry)
*CHIRALITY
- Language
- ISSN
- 0044-8249
Abstract: Stereospecific nucleophilic substitution was achieved for the first time with arylboronic acids as nucleophiles. This transition‐metal‐free coupling between chiral α‐aryl‐α‐mesylated acetamides and arylboronic acids provided access to a series of chiral α,α‐diaryl acetamides with excellent enantioselectivity and moderate to good yields. The CONH functionality proved to be crucial for bridging the reactants and promoting the reaction. Efficient syntheses of a cannabinoid CB1 receptor ligand, the antidepressant (S)‐diclofensine, and a key chiral building block of the inhibitor implitapide were successfully accomplished by using this method. [ABSTRACT FROM AUTHOR]