120696-98-2Relevant articles and documents
A simple route to 3-substituted 2-cyano allylic alcohols
Aiai, Mouna,Baudy-Floc'h, Michèle,Robert, Albert,Le Grel, Philippe
, p. 403 - 406 (1996)
The first original and simple route to 3-substituted 2-cyano allylic alcohols with very good yields is described. The epoxide function in the key step acts as a protecting group during the synthesis of these allylic alcohols.
A new and efficient method for the isomerization of secondary functional allylic alcohols into their primary isomers
Beltaief, Imen,Hbaieb, Souhaira,Besbes, Rafaa,Amri, Hassen,Villieras, Monique,Villieras, Jean
, p. 1765 - 1768 (2007/10/03)
The first efficient tandem: 'bromination-formylation-hydrolysis' for the 1,3-transposition of acyclic allylic alcohols 1 and 2 bearing a nitrile and an ester group is reported.
The Stereochemistry of Organometallic Compounds. XXXI Hydrocyanation of Alkynols
Jackson, W. Roy,Lovel, Craig G.,Perlmutter, Patrick,Smallridge, Andrew J.
, p. 1099 - 1106 (2007/10/02)
The regioselectivity of hydrocyanation of a range of alkynols using nickel-based catalyst systems involving either triphenyl phosphite or α,α'-bis(diphenylphosphino)-o-xylene (phmep) has been investigated.The regioselectivity of the hydrocyanations involv
