Chirality 2014-12-01

Direct asymmetric anti-Mannich-type reactions catalyzed by cinchona alkaloid derivatives.

Ying Jin, Di Chen, Xiu Rong Zhang

文献索引:Chirality 26(12) , 801-5, (2014)

全文:HTML全文

摘要

A series of cinchona alkaloid derivatives were used to catalyze the asymmetric anti-Mannich-type reaction of 3-methyl-2-oxindole with N-tosyl aryl aldimines. The resulting anti-3,3-disubstituted 2-oxindole products were obtained in good yields (up to 92%) with high diastereo- and enantioselectivities (anti/syn up to 97:3 and 91% ee).© 2014 Wiley Periodicals, Inc.


相关化合物

  • 3-甲基羟基吲哚

相关文献:

Metabolism of 3-methylindole by vaccinia-expressed P450 enzymes: correlation of 3-methyleneindolenine formation and protein-binding.

1996-01-01

[J. Pharmacol. Exp. Ther. 276(1) , 21-9, (1996)]

Unbiased high-throughput screening of reactive metabolites on the linear ion trap mass spectrometer using polarity switch and mass tag triggered data-dependent acquisition.

2008-08-15

[Anal. Chem. 80(16) , 6410-22, (2008)]

Metabolism and pneumotoxicity of 3-methyloxindole, indole-3-carbinol, and 3-methylindole in goats.

1982-08-01

[Am. J. Vet. Res. 43(8) , 1418-23, (1982)]

Porcine CYP2A19, CYP2E1 and CYP1A2 forms are responsible for skatole biotransformation in the reconstituted system.

2009-01-01

[Neuro Endocrinol. Lett. 30 Suppl 1 , 36-40, (2009)]

Facile and Efficient Enantioselective Hydroxyamination Reaction: Synthesis of 3-Hydroxyamino-2-Oxindoles Using Nitrosoarenes. Shen K, et al.

[Angew. Chem. Weinheim Bergstr. Ger. 123(20) , 4780-4784, (2011)]

更多文献...