Readily Accessible, Modular, and Tuneable BINOL 3,3‘-Perfluoroalkylsulfones:  Highly Efficient Catalysts for Enantioselective In-Mediated Imine Allylation

Robert Kargbo; Yoko Takahashi; Santosh Bhor; Gregory R. Cook; Guy C. Lloyd-Jones; Ian R. Shepperson

doi:10.1021/ja070742t

journal article Mar 13, 2007

Readily Accessible, Modular, and Tuneable BINOL 3,3‘-Perfluoroalkylsulfones: Highly Efficient Catalysts for Enantioselective In-Mediated Imine Allylation

Robert Kargbo Yoko Takahashi Santosh Bhor Gregory R. Cook Guy C. Lloyd-Jones

Ian R. Shepperson

Journal of the American Chemical Society Vol. 129 No. 13 pp. 3846-3847 · American Chemical Society (ACS)

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References

28

[1]

Nucleophilic Chem. Rev (1999) 10.1021/cr980414z

[2]

Recent J. Org. Chem (1999) 10.1021/jo990238+

[3]

Berger R. J. Am. Chem. Soc (2003) 10.1021/ja035001g

[4]

Berger R. J. Am. Chem. Soc (2004) 10.1021/ja0486418

[5]

Kobayashi S. J. Am. Chem. Soc (2003) 10.1021/ja035061m

[6]

For Tetrahedron Lett (1992) 10.1016/s0040-4039(00)61099-7

[7]

Cooper I. R. Chem. Commun (2002) 10.1039/b202940e

[8]

Cooper I. R. Tetrahedron Lett (2003) 10.1016/s0040-4039(03)00277-6

[9]

Basile T. J. Org. Chem (1994) 10.1021/jo00104a037

[10]

Loh T.-P. Tetrahedron Lett (1997) 10.1016/s0040-4039(96)02427-6

[11]

Vilaivan T. J. Org. Chem (2005) 10.1021/jo0477244

[12]

Lee J. G. J. Chem. Soc., Perkin Trans. (2002) 10.1039/b110505c

[13]

Miyabe H. Chem. Commun (2002) 10.1039/b203493j

[14]

Miyabe H. J. Org. Chem (2003) 10.1021/jo034451o

[15]

Miyabe H. J. Org. Chem (2004) 10.1021/jo035442i

[16]

Cook G. R. Org. Lett (2004) 10.1021/ol0496172

[17]

For (2002)

[18]

Cook G. R. Org. Lett (2005) 10.1021/ol051160o

[19]

For Tetrahedron Lett (1999) 10.1016/s0040-4039(99)01743-8

[20]

Tan K. L. Angew. Chem., Int. Ed (2007) 10.1002/anie.200603354

[21]

Chan T. H. J. Am. Chem. Soc (1999) 10.1021/ja984359n

[22]

Araki S. J. Organomet. Chem (1989) 10.1016/0022-328x(89)85180-0

[23]

A survey of Hammett substituent constants and resonance and field parameters

Corwin. Hansch, A. Leo, R. W. Taft

Chemical Reviews 1991 10.1021/cr00002a004

[24]

Charmant J. P. H. Chem. Commun (2003) 10.1039/b210648e

[25]

Zhao Z. Chem. Commun (2006) 10.1039/b606092g

[26]

Steensma R. W. Tetrahedron Lett (2001) 10.1016/s0040-4039(01)00164-2

[27]

Kozlowski J. Org. Chem (2003) 10.1021/jo020401s

[28]

For (2004)

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Details

Published: Mar 13, 2007
Vol/Issue: 129(13)
Pages: 3846-3847

Authors

R

Robert Kargbo