Enantioselective conjugate radical addition reactions mediated by chiral Lewis acid complexes of (R,R)-4,6-dibenzofurandiyl-2,2′-bis(4-phenyloxazoline) (DBFOX/Ph)

1999 ◽  
Vol 10 (12) ◽  
pp. 2417-2428 ◽  
Author(s):  
Ulrich Iserloh ◽  
Dennis P Curran ◽  
Shuji Kanemasa
2013 ◽  
Vol 9 ◽  
pp. 1148-1155 ◽  
Author(s):  
Hideto Miyabe ◽  
Ryuta Asada ◽  
Yoshiji Takemoto

The limitation of hydroxamate ester as a chiral Lewis acid coordination moiety was first shown in an intermolecular reaction involving a radical addition and sequential allylation processes. Next, the effect of hydroxamate ester was studied in the cascade addition–cyclization–trapping reaction of substrates with a carbon–carbon triple bond as a radical acceptor. When substrates with a methacryloyl moiety and a carbon–carbon triple bond as two polarity-different radical acceptors were employed, the cascade reaction proceeded effectively. A high level of enantioselectivity was also obtained by a proper combination of chiral Lewis acid and these substrates.


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

1994 ◽  
Vol 67 (10) ◽  
pp. 2785-2794 ◽  
Author(s):  
Ikuo Shinoda ◽  
Akihiko Takahashi ◽  
Takao Saito ◽  
Tokiko Uchida

2004 ◽  
Vol 126 (17) ◽  
pp. 5366-5367 ◽  
Author(s):  
Mukund P. Sibi ◽  
Kennosuke Itoh ◽  
Craig P. Jasperse

ChemInform ◽  
2006 ◽  
Vol 37 (12) ◽  
Author(s):  
Shih-Yuan Liu ◽  
Ivory D. Hills ◽  
Gregory C. Fu

Tetrahedron ◽  
1965 ◽  
Vol 21 (10) ◽  
pp. 2743-2747 ◽  
Author(s):  
H. Goldwhite ◽  
M.S. Gibson ◽  
C. Harris

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