1369956-71-7Relevant academic research and scientific papers
S,O-ligand-promoted palladium-catalyzed C–H olefination of arenes with allylic substrates
Naksomboon, Kananat,álvarez-Casao, Yolanda,Uiterweerd, Michiel,Westerveld, Nick,Maciá, Beatriz,Fernández-Ibá?ez, M. ángeles
supporting information, p. 379 - 382 (2017/12/28)
An efficient catalytic system for the C–H olefination of arenes with different allylic substrates is reported. The catalytic system is based on Pd(OAc)2 and a readily accessible bidentate S,O-ligand. The methodology shows high activity with a wide range of arenes, including bulky and, electron-rich and -poor arenes. The applicability of this catalyst is demonstrated in the late-stage functionalization of the complex molecule O-methylestrone.
Pd-catalyzed oxidative olefination of arenes with olefins via C-H activation: Retention of the leaving group
Mao, Jincheng,Yang, Xiaojiang,Wang, Dingli,Zhang, Yang
, p. 2050 - 2055 (2016/03/19)
Pd-catalyzed direct oxidative olefination of arenes with olefins via C-H activation is described in the absence of any chelating directing groups. For Pd-catalyzed oxidative coupling between arenes and allyl acetate, it was observed the retention of the leaving group.
Stille couplings in water at room temperature
Lu, Guo-Ping,Cai, Chun,Lipshutz, Bruce H.
supporting information, p. 105 - 109 (2013/02/23)
A nonionic amphiphile, TPGS-750-M, enables efficient Stille couplings between a wide range of substrates to be conducted in water as the only medium, in most cases at room temperature.
Pd(II)-catalyzed direct olefination of arenes with allylic esters and ethers
Shang, Xiaojie,Xiong, Yun,Zhang, Yuexia,Zhang, Lei,Liu, Zhongquan
supporting information; experimental part, p. 259 - 262 (2012/03/08)
A convenient Pd(II)-catalyzed direct olefination of unactivated arenes with allylic esters and ethers via C-H activation was demonstrated. Under the typical conditions, various aryl-substituted allylic esters and ethers can be prepared. Georg Thieme Verlag Stuttgart - New York.
Triflimide-catalyzed allyl-allyl cross-coupling: A metal-free allylic alkylation
Ding, Feiqing,William, Ronny,Wang, Fei,Liu, Xue-Wei
supporting information; experimental part, p. 8709 - 8711 (2012/10/08)
A highly efficient metal-free intermolecular C(sp3)-C(sp3) allyl-allyl cross-coupling protocol between allyl acetates and allyltrimethylsilanes, which proceeded smoothly in the presence of catalytic triflimide to form 1,5-dienes with good to excellent regioselectivity, has been developed.
