| Literature DB >> 30964216 |
Nivesh Kumar1, Reddy Rajasekhar Reddy1, Ahmad Masarwa1.
Abstract
An efficient and general method for the chemoselective synthesis of unsymmetrical gem-diborylalkanes is reported. This method is based on a late-stage desymmetrization through nucleophilic "trifluorination", providing chiral gem-diborylalkanes bearing a trifluoroborate group. The reaction offers a highly modular and diastereoselective approach towards the synthesis of gem-diborylcyclopropanes. The utility of the gem-diborylalkane building blocks was demonstrated by selective post-functionalization of the trifluoroborate group. These functionalizations include inter- and intra- Pd-catalyzed Suzuki-Miyaura coupling reactions.Entities:
Keywords: Suzuki-Miyaura cross-coupling; cyclopropanes; desymmetrization; gem-diborylalkanes; organotrifluoroborate salts
Year: 2019 PMID: 30964216 DOI: 10.1002/chem.201901267
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236