6974-04-5Relevant articles and documents
Nickel-catalyzed cross-coupling of unactivated alkyl halides using bis(pinacolato)diboron as reductant
Xu, Hailiang,Zhao, Chenglong,Qian, Qun,Deng, Wei,Gong, Hegui
, p. 4022 - 4029 (2013/09/23)
The use of bis(pinacolato)diboron as the terminal reductant allows the efficient Ni-catalyzed coupling of unactivated secondary and primary alkyl halides, generating the C(sp3)-C(sp3) coupling products in good yields. The mild cataly
OXIDATION OF BENZYL ETHER TO BENZOATE BY OZONE
Hirama, Masahiro,Shimizu, Mitsuaki
, p. 781 - 786 (2007/10/02)
Ozoniation of benzyl ethers at low temperatures in acetone or methanol solvent smoothly gave the corresponding benzoates in good yields.