25634-92-8Relevant academic research and scientific papers
A versatile palladium catalyst system for Suzuki-Miyaura coupling of alkenyl tosylates and mesylates
Wong, Pui Yu,Chow, Wing Kin,Chung, Kin Ho,So, Chau Ming,Lau, Chak Po,Kwong, Fuk Yee
supporting information; experimental part, p. 8328 - 8330 (2011/09/14)
A general and effective palladium system for Suzuki-Miyaura coupling of alkenyl electrophiles under mild reaction conditions is reported. With the Pd(OAc)2/CM-phos system, a variety of alkenyl tosylates are coupled well with ArB(OH)2. Moreover, the first successful examples of using alkenyl mesylates in alkenylation are also described.
Modern Friedel-Crafts chemistry. XVI. Sterically controlled cyclodehydration of selected arylalkanols
Khawaga, A. M. El-,Zohry, M. F. El-,Wahab, A. A. Abdel-,Khalaf, A. A.
, p. 1051 - 1055 (2007/10/02)
The cyclodehydration of three selected arylalkanols, namely 1,3-diphenyl-3-pentanol (I), 1,1,4-triphenyl-2methyl-1-butanol (II) and 1,1,4-triphenyl-2-methyl-2-butanol (III) with Friedel-Crafts catalysts was investigated.A reasonable interpretation of the reaction products was suggested, steric hindrance was found to have major influence on the course of the reaction.
