16704-20-4Relevant academic research and scientific papers
ANTI STEREOCHEMISTRY IN PROTODESILYLATION OF AN OPTICALLY ACTIVE ALLYLSILANE WITH TRRIFLUOROACETIC ACID-D
Hayashi, Tamio,Ito, Hiroshi,Kumada, Makoto
, p. 4605 - 4606 (1982)
SE' reaction of (R)-(E)-1,3-diphenyl-3-trimethylsilylpropene with trifluoroacetic acid-d proceeded with anti stereochemistry to give (R)-(E)-1,3-diphenylpropene-3-d.
Direct Reduction of Allylic Alcohols Using Isopropanol as Reductant
Sai, Masahiro
supporting information, p. 3482 - 3487 (2018/09/14)
The lithium cation-catalyzed direct reduction of allylic alcohols to alkenes using isopropanol as a hydride donor was developed. The hydride transfer of the in situ-generated lithium isopropoxide to an allylic cation is the key process in this transformation. The reaction generates only water and acetone as byproducts, which highlights the synthetic utility of this method. (Figure presented.).
FeCl3 · 6H2O catalyzed disproportionation of allylic alcohols and selective allylic reduction of allylic alcohols and their derivatives with benzyl alcohol
Wang, Jialiang,Huang, Wen,Zhang, Zhengxing,Xiang, Xu,Liu, Ruiting,Zhou, Xigeng
supporting information; experimental part, p. 3299 - 3304 (2009/09/08)
Iron chloride has been found to be an efficient catalyst for the disproportionation of allylic alcohols, which provides a convenient method for selective transformation of allylic alcohols to alkenes and α,β- unsaturated ketones. Furthermore, this catalytic system is also effective for highly selective allylic reduction of allylic alcohols, allylic ethers, and allylic acetates with benzyl alcohol under neutral and convenient reaction conditions.
Preparation of meso-1,3-diphenylallyllithium·(-)-sparteine - Its crystal structure and reactions
Marr, Felix,Froehlich, Roland,Hoppe, Dieter
, p. 2587 - 2592 (2007/10/03)
The X-ray crystal structure of 1,3-diphenylallyllithium, complexed with enantiomerically pure (-)-sparteine, was determined. The crystallized complex is stereohomogeneous. Its subsequent electrophilic substitution reactions proceed with low enantioselecti
