57415-92-6Relevant articles and documents
Primary Alcohols via Nickel Pentacarboxycyclopentadienyl Diamide Catalyzed Hydrosilylation of Terminal Epoxides
Lambert, Tristan H.,Steiniger, Keri A.
supporting information, p. 8013 - 8017 (2021/10/25)
The efficient and regioselective hydrosilylation of epoxides co-catalyzed by a pentacarboxycyclopentadienyl (PCCP) diamide nickel complex and Lewis acid is reported. This method allows for the reductive opening of terminal, monosubstituted epoxides to form unbranched, primary alcohols. A range of substrates including both terminal and nonterminal epoxides are shown to work, and a mechanistic rationale is provided. This work represents the first use of a PCCP derivative as a ligand for transition-metal catalysis.
Phenylthioallyl and Phenylthiovinyl Phosphine Oxides: Synthesis of 1-Phenylthiobutadienes and a Three-component Synthesis of Ketones
Grayson, J. Ian,Warren, Stuart,Zaslona, Alex T.
, p. 967 - 976 (2007/10/02)
The functionalisation of some substituted allyl and vinyl diphenylphosphine oxides is explored and routes to substituted γ-phenylthioallyl and γ-phenylthiovinyl phosphine oxides are described.These reagents are used in the synthesis of the title compounds.
