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 ◽  
...  
Synlett ◽  
1998 ◽  
Vol 1998 (10) ◽  
pp. 1053-1056 ◽  
Author(s):  
Kazuaki Ishihara ◽  
Kazato Inanaga ◽  
Shoichi Kondo ◽  
Miyuki Funahashi ◽  
Hisashi Yamamoto

ChemInform ◽  
2003 ◽  
Vol 34 (46) ◽  
Author(s):  
Tetsuji Hayano ◽  
Toshiaki Sakaguchi ◽  
Hiroshi Furuno ◽  
Masaaki Ohba ◽  
Hisashi Okawa ◽  
...  

2003 ◽  
Vol 32 (7) ◽  
pp. 608-609 ◽  
Author(s):  
Tetsuji Hayano ◽  
Toshiaki Sakaguchi ◽  
Hiroshi Furuno ◽  
Masaaki Ohba ◽  
Hisashi Okawa ◽  
...  

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

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.


Sign in / Sign up

Export Citation Format

Share Document