Chemical Communications 2012-02-28

Asymmetric assembly of 2-oxindole and α-angelica lactone units to construct vicinal quaternary chiral centers.

Xin Huang, Jin Peng, Lin Dong, Ying-Chun Chen

Index: Chem. Commun. (Camb.) 48(18) , 2439-41, (2012)

Full Text: HTML

Abstract

The first organocatalytic asymmetric assembly of Morita-Baylis-Hillman carbonates of isatins and α-angelica lactone has been studied, affording multifunctional products containing two valuable pharmacophores and vicinal quaternary chiral centers in high stereoselectivity (up to 92% ee, dr >95:5).This journal is © The Royal Society of Chemistry 2012


Related Compounds

Related Articles:

Characterization of the PON1 active site using modeling simulation, in relation to PON1 lactonase activity

2008-01-01

[Bioorg. Med. Chem. 16 , 7504-9, (2008)]

Enhancement of rat hepatic and gastrointestinal glutathione and glutathione S-transferases by alpha-angelicalactone and flavone.

1995-03-01

[Carcinogenesis 16(3) , 607-12, (1995)]

Catalytic asymmetric vinylogous Mannich-type (AVM) reaction of nonactivated α-angelica lactone.

2011-06-17

[Org. Lett. 13(12) , 3056-9, (2011)]

Effect of butylated hydroxyanisole, alpha-angelica lactone, and beta-naphthoflavone on benzo(alpha)pyrene:DNA adduct formation in vivo in the forestomach, lung, and liver of mice.

1982-04-01

[Cancer Res. 42(4) , 1199-204, (1982)]

More Articles...