| Literature DB >> 29963866 |
Yohei Ogiwara1, Yuka Sakurai1, Hiroyuki Hattori1, Norio Sakai1.
Abstract
Ligand-controlled non-decarbonylative and decarbonylative conversions of acyl fluorides were developed using a Pd(OAc)2/Et3SiH combination. When tricyclohexylphosphine (PCy3) was used as the ligand, aldehydes were obtained as simple reductive conversion products. The use of 1,2-bis(dicyclohexylphosphino)ethane (Cy2P(CH2)2PCy2, DCPE) as the ligand, however, favored the formation of hydrocarbons, which are decarbonylative reduction products.Entities:
Year: 2018 PMID: 29963866 DOI: 10.1021/acs.orglett.8b01582
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005