Boronic Acid Catalysis as a Mild and Versatile Strategy for Direct Carbo??and Heterocyclizations of Free Allylic Alcohols
H Zheng, S Ghanbari, S Nakamura…
Index: Zheng, Hongchao; Ghanbari, Sina; Nakamura, Shinji; Hall, Dennis G. Angewandte Chemie - International Edition, 2012 , vol. 51, # 25 p. 6187 - 6190
Full Text: HTML
Citation Number: 39
Abstract
The ability to activate simple electrophilic functional groups directly without recourse to intermediary functionalities like halides and pseudohalides (eg, sulfonates, oxyphosphonium) has become an important goal of modern organic chemistry.[1] Boronic acid catalysis (BAC) is emerging as a mild and effective strategy for the direct, covalent activation of alcohols and carboxylic acids.[2] Important reactions such as direct ...
Related Articles:
[Singh, Parvinder Pal; Gudup, Satish; Aruri, Hariprasad; Singh, Umed; Ambala, Srinivas; Yadav, Mahipal; Sawant, Sanghapal D.; Vishwakarma, Ram A. Organic and Biomolecular Chemistry, 2012 , vol. 10, # 8 p. 1587 - 1597]
PdII??katalysierte regioselektive Arylchlorierung und Oxyarylierung ungesättigter Alkohole
[Tamaru, Yoshinao; Hojo, Makoto; Higashimura, Hideyuki; Yoshida, Zen-ichi Angewandte Chemie, 1986 , vol. 98, # 8 p. 740 - 742]
[Harwood, Laurence M.; Robertson, Jeremy Tetrahedron Letters, 1987 , vol. 28, # 43 p. 5175 - 5176]
[Inoue, Atsushi; Shinokubo, Hiroshi; Oshima, Koichiro Synlett, 1999 , # 10 p. 1582 - 1584]
[He, Ruoyu; Jin, Xiqing; Chen, Hui; Huang, Zhi-Tang; Zheng, Qi-Yu; Wang, Congyang Journal of the American Chemical Society, 2014 , vol. 136, # 18 p. 6558 - 6561]