ChemInform Abstract: [(Indenyl)Ru(biphop-F)]+: A Lewis Acid Catalyst that Controls Both the Diene and the Dienophile Facial Selectivity in Diels-Alder Reactions.

ChemInform ◽  
2010 ◽  
Vol 33 (18) ◽  
pp. no-no
Author(s):  
E. Peter Kuendig ◽  
Christophe M. Saudan ◽  
Valerie Alezra ◽  
Florian Viton ◽  
Gerald Bernardinelli
2001 ◽  
Vol 113 (23) ◽  
pp. 4613-4617 ◽  
Author(s):  
E. Peter Kündig ◽  
Christophe M. Saudan ◽  
Valérie Alezra ◽  
Florian Viton ◽  
Gérald Bernardinelli

Tetrahedron ◽  
2012 ◽  
Vol 68 (6) ◽  
pp. 1774-1781 ◽  
Author(s):  
Chigusa Seki ◽  
Masafumi Hirama ◽  
N.D.M. Romauli Hutabarat ◽  
Junko Takada ◽  
Chonticha Suttibut ◽  
...  

2006 ◽  
Vol 47 (6) ◽  
pp. 873-875 ◽  
Author(s):  
Taichi Kano ◽  
Teppei Konishi ◽  
Shunsuke Konishi ◽  
Keiji Maruoka

Tetrahedron ◽  
2006 ◽  
Vol 62 (49) ◽  
pp. 11397-11401 ◽  
Author(s):  
Katsumi Kubota ◽  
Christopher L. Hamblett ◽  
Xiaolun Wang ◽  
James L. Leighton

2019 ◽  
Vol 15 ◽  
pp. 1304-1312 ◽  
Author(s):  
Qichao Zhang ◽  
Jian Lv ◽  
Sanzhong Luo

The combination of the trityl cation and a chiral weakly coordinating Fe(III)-based bisphosphate anion was used to develop a new type of a highly active carbocation Lewis acid catalyst. The stereocontrol potential of the chiral tritylium ion pair was demonstrated by its application in an enantioselective Diels–Alder reaction of anthracene.


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