1200184-41-3Relevant academic research and scientific papers
Rhodium-catalyzed asymmetric ring opening reaction of oxabenzonorbornadienes with amines using ZnI2 as the activator
Xu, Xin,Chen, Jingchao,He, Zhenxiu,Zhou, Yongyun,Fan, Baomin
, p. 2480 - 2486 (2016)
The complex of [Rh(COD)Cl]2 and (R,R)-BDPP was used as an effective catalyst for the asymmetric ring opening reaction of oxabenzonorbornadienes with various amines by employing ZnI2 as the activator. Under the optimized reaction cond
Asymmetric ring opening reaction of oxabenzonorbornadienes with amines promoted by iridium/NMDPP complex
Yu, Lu,Zhou, Yongyun,Xu, Xin,Li, Sifeng,Xu, Jianbin,Fan, Baomin,Lin, Chengyuan,Bian, Zhaoxiang,Chan, Albert S.C.
supporting information, p. 6315 - 6318 (2014/12/11)
As an efficient catalyst, the [Ir(COD)Cl]2/NMDPP complex has been successfully applied to promote the asymmetric ring opening reaction of oxabenzonorbornadienes with various amines, which afforded the corresponding products in good yields (72-9
Asymmetric ring-opening of oxabenzonorbornadiene with amines promoted by a chiral iridium-monophosphine catalyst
Luo, Renshi,Liao, Jianhua,Xie, Ling,Tang, Wenjun,Chan, Albert S. C.
supporting information, p. 9959 - 9961 (2013/10/22)
A new iridium-monophosphine catalyst is found to be efficient for asymmetric ring-opening of benzonorbornadiene with amines, providing a series of chiral substituted dihydronaphthalenes in high yields (up to 98%) and excellent enantioselectivities (>99%).
Iridium-catalyzed asymmetric ring-opening reactions of oxabicyclic alkenes with secondary amine ucleophiles
Yang, Dingqiao,Hu, Ping,Long, Yuhua,Wu, Yujuan,Zeng, Heping,Wang, Hui,Zuo, Xiongjun
supporting information; experimental part, (2010/04/22)
Iridium-catalyzed asymmetric ring-opening reactions of oxabicyclic alkenes with various aliphatic and aromatic secondary amines are reported for the first time. The reaction gave the corresponding trans-1,2-dihydronaphthalenol derivatives in good yields w
