| Literature DB >> 29542928 |
Guisheng Li1, Olga V Zatolochnaya1, Xiao-Jun Wang1, Sonia Rodríguez1, Bo Qu1, Jean-Nicolas Desrosiers1, Hari P R Mangunuru1, Soumik Biswas1, Daniel Rivalti1, Shuklendu D Karyakarte1, Joshua D Sieber1, Nelu Grinberg1, Ling Wu1, Heewon Lee1, Nizar Haddad1, Daniel R Fandrick1, Nathan K Yee1, Jinhua J Song1, Chris H Senanayake1.
Abstract
Novel bidentate phosphine ligands BABIPhos featuring a biaryl bis-dihydrobenzooxaphosphole core are presented. Their synthesis was achieved via Pd-catalyzed reductive homocoupling of dihydrobenzooxaphosphole aryl triflates. An efficient route toward various analogues was also established, giving access to phosphines with different electronic and steric properties. The newly obtained ligands demonstrated high efficiency and selectivity in Rh-catalyzed asymmetric hydrogenation of di- and trisubstituted enamides. This new class of ligands is complementary to previously described bidentate benzooxaphosphole ligands BIBOP.Entities:
Year: 2018 PMID: 29542928 DOI: 10.1021/acs.orglett.8b00139
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005