914247-45-3Relevant academic research and scientific papers
Palladium- and base-free synthesis of conjugated ynones by cross-coupling reactions of alkynylboronates with acid chlorides mediated by CuCl
Nishihara, Yasushi,Saito, Daisuke,Inoue, Eiji,Okada, Yoshiaki,Miyazaki, Mikihiro,Inoue, Yoshiaki,Takagi, Kentaro
, p. 306 - 308 (2010)
Alkynylboronates can be employed as a practical and versatile precursor for a variety of π-conjugated organic compounds. In the presence of Cu(I) salt, cross-coupling reactions of acid chlorides with alkynylboronates giving rise to the corresponding conju
Rhenium-catalyzed 1,3-isomerization of allylic alcohols: Scope and chirality transfer
Morrill, Christie,Beutner, Gregory L.,Grubbs, Robert H.
, p. 7813 - 7825 (2007/10/03)
(Chemical Equation Presented) The scope of the triphenylsilyl perrhennate (O3ReOSiPh3, 1) catalyzed 1,3-isomerization of allylic alcohols has been thoroughly explored. It was found to be effective for a wide variety of secondary and tertiary allylic alcohol substrates bearing aryl, alkyl, and cyano substituents. Two general reaction types were found which gave high levels of product selectivity: those driven by formation of an extended conjugated system and those driven by selective silylation of a particular isomer. The efficiency of chirality transfer with various substrates was investigated, and conditions were found in which secondary and tertiary allylic alcohols could be formed with high levels of enantioselectivity. Consideration of selectivity trends with respect to the nature of the substituents around the allylic system revealed that this is a reliable and predictable method for allylic alcohol synthesis.
