[(Indenyl)Ru(biphop-F)]+: A Lewis Acid Catalyst That Controls both the Diene and the Dienophile Facial Selectivity in Diels–Alder Reactions This work was supported by the Swiss National Science Foundation (FNS grant 20-59374.99) and The Ministère des Affaires Etrangères from France (Lavoisier grant to V.A.). biphop-F=1,2-bis[bis(pentafluorophenyl)phosphanyloxy]-1,2-diphenylethane.

2001 ◽  
Vol 40 (23) ◽  
pp. 4481 ◽  
Author(s):  
E. Peter Kündig ◽  
Christophe M. Saudan ◽  
Valérie Alezra ◽  
Florian Viton ◽  
Gérald Bernardinelli
Keyword(s):  
Lewis Acid ◽  
National Science Foundation ◽  
Acid Catalyst ◽  
Diels Alder ◽  
Swiss National Science Foundation ◽  
Facial Selectivity ◽  
National Science ◽  
Lewis Acid Catalyst

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
Keyword(s):  
Lewis Acid ◽  
Acid Catalyst ◽  
Diels Alder ◽  
Facial Selectivity ◽  
Lewis Acid Catalyst

[(Indenyl)Ru(biphop-F)]+: A Lewis Acid Catalyst That Controls both the Diene and the Dienophile Facial Selectivity in Diels-Alder Reactions

2001 ◽  
Vol 113 (23) ◽  
pp. 4613-4617 ◽  
Author(s):  
E. Peter Kündig ◽  
Christophe M. Saudan ◽  
Valérie Alezra ◽  
Florian Viton ◽  
Gérald Bernardinelli
Keyword(s):  
Lewis Acid ◽  
Acid Catalyst ◽  
Diels Alder ◽  
Facial Selectivity ◽  
Lewis Acid Catalyst

Asymmetric synthesis of isoquinuclidines by Diels–Alder reaction of 1,2-dihydropyridine utilizing a chiral Lewis acid catalyst

Tetrahedron ◽  
2012 ◽  
Vol 68 (6) ◽  
pp. 1774-1781 ◽  
Author(s):  
Chigusa Seki ◽  
Masafumi Hirama ◽  
N.D.M. Romauli Hutabarat ◽  
Junko Takada ◽  
Chonticha Suttibut ◽  
...  
Keyword(s):  
Asymmetric Synthesis ◽  
Lewis Acid ◽  
Acid Catalyst ◽  
Alder Reaction ◽  
Diels Alder ◽  
Diels Alder Reaction ◽  
Chiral Lewis Acid ◽  
Lewis Acid Catalyst

Design of chiral tin(IV) aryloxide as a mild Lewis acid catalyst for enantioselective Diels–Alder reaction

2006 ◽  
Vol 47 (6) ◽  
pp. 873-875 ◽  
Author(s):  
Taichi Kano ◽  
Teppei Konishi ◽  
Shunsuke Konishi ◽  
Keiji Maruoka
Keyword(s):  
Lewis Acid ◽  
Acid Catalyst ◽  
Alder Reaction ◽  
Diels Alder ◽  
Diels Alder Reaction ◽  
Lewis Acid Catalyst

Strained silacycle-catalyzed asymmetric Diels–Alder cycloadditions: the first highly enantioselective silicon Lewis acid catalyst

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

scholarly journals Enantioselective Diels–Alder reaction of anthracene by chiral tritylium catalysis

2019 ◽  
Vol 15 ◽  
pp. 1304-1312 ◽  
Author(s):  
Qichao Zhang ◽  
Jian Lv ◽  
Sanzhong Luo
Keyword(s):  
Lewis Acid ◽  
Acid Catalyst ◽  
Alder Reaction ◽  
Ion Pair ◽  
Diels Alder ◽  
Highly Active ◽  
Diels Alder Reaction ◽  
New Type ◽  
Lewis Acid Catalyst ◽  
Trityl Cation

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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