14004-19-4Relevant articles and documents
Z Stereoselective Wittig Olefination of 2-Oxygenated Cyclohexanones
Koreeda, Masato,Patel, Paresh D.,Brown, Lindsey
, p. 5910 - 5912 (1985)
Protected 2-hydroxy- and 2,3-epoxycyclohexanones provided (Z)-ethylidenecyclohexanes in a highly stereoselective manner upon their reactions with ethylidenetriphenylphosphorane in both the lithium base and the lithium-free conditions of the Wittig reactio
Titanium tetrachloride promoted cyclodehydration of aryloxyketones: Facile synthesis of benzofurans and naphthofurans with high regioselectivity
Zhang, Qiu,Luo, Juan,Wang, Bingqiao,Xiao, Xiaoqin,Gan, Zongjie,Tang, Qiang
supporting information, p. 1337 - 1340 (2019/04/16)
An efficient and facile method for the synthesis of a broad series of benzofurans and naphthofurans is described. The direct intramolecular cyclodehydration of aryloxyketones in the presence of titanium tetrachloride affords the corresponding benzofurans and naphthofurans with good regioselectivity and yields.
Enantioselective synthesis of chiral β-aryloxy alcohols by ruthenium-catalyzed ketone hydrogenation via dynamic kinetic resolution (DKR)
Bai, Wen-Ju,Xie, Jian-Hua,Li, Ya-Li,Liu, Sheng,Zhou, Qi-Lin
supporting information; experimental part, p. 81 - 84 (2010/06/16)
A highly efficient enantioselective synthesis of chiral β-aryloxy alcohols by the [RuCl2[(S)-SDP][(R, R)-DPEN]} [(Sa,R, R)-1a; SDP = 7, 7′-bis-(diarylphosphino)-1,1′-spirobiindane; DPEN = trans-1,2-diphenylethylenediamine] complex-ca
