1370729-64-8Relevant articles and documents
Recyclable Poly-Zn3(OAc)4-3,3′-Bis(aminoimino)binaphthoxide Catalyst for Asymmetric Iodolactonization
Arai, Takayoshi,Kojima, Takahiro,Watanabe, Ohji,Itoh, Tsutomu,Kanoh, Hirofumi
, p. 3234 - 3238 (2015/10/28)
On the basis of the structure of the unimolecular Zn3(OAc)4-3,3′-bis(aminoimino)binaphthoxide complex, a poly-Zn3(OAc)4-3,3′-bis(aminoimino)binaphthoxide (poly-Zn) complex was prepared from 3,3′-diformylbinaphth
A trinuclear Zn3(OAc)4-3,3′-bis(aminoimino) binaphthoxide complex for highly efficient catalytic asymmetric iodolactonization
Arai, Takayoshi,Sugiyama, Noriyuki,Masu, Hyuma,Kado, Sayaka,Yabe, Shinnosuke,Yamanaka, Masahiro
supporting information, p. 8287 - 8290 (2014/07/22)
A 3,3′-bis(aminoimino)BINOL ligand was newly designed and synthesized for the formation of a trinuclear Zn complex upon reaction with Zn(OAc) 2. Using the harmony of the tri-zinc atoms, 1 mol% Zn 3(OAc)4-3,3′-bis(aminoimin
Asymmetric iodolactonization utilizing chiral squaramides
Tungen, Jorn E.,Nolsoe, Jens M. J.,Hansen, Trond V.
, p. 5884 - 5887 (2013/02/23)
Asymmetric iodolactonization of γ- and δ-unsaturated carboxylic acids has been explored in the presence of six different chiral organocatalysts 5-8. The catalyst 6b was found to facilitate the cyclization of 5-arylhex-5-enoic acids 1 to the corresponding
