Angewandte Chemie. International edition in English 2012-04-27

An efficient flow-photochemical synthesis of 5H-furanones leads to an understanding of torquoselectivity in cyclobutenone rearrangements.

David C Harrowven, Mubina Mohamed, Théo P Gonçalves, Richard J Whitby, David Bolien, Helen F Sneddon

Index: Angew. Chem. Int. Ed. Engl. 51(18) , 4405-8, (2012)

Full Text: HTML

Abstract

Related Compounds

Related Articles:

Norfuraneol dephosphorylates eNOS at threonine 495 and enhances eNOS activity in human endothelial cells.

2009-03-01

[Cardiovasc. Res. 81(4) , 750-7, (2009)]

Investigation of the reaction between 4-hydroxy-5-methyl-3(2H)-furanone and cysteine or hydrogen sulfide at pH 4.5.

1999-04-01

[J. Agric. Food Chem. 47(4) , 1626-34, (1999)]

Heterocyclic volatiles formed by heating cysteine or hydrogen sulfide with 4-hydroxy-5-methyl-3(2H)-furanone at pH 6.5.

2001-02-01

[J. Agric. Food Chem. 49(2) , 816-22, (2001)]

Maillard reaction products modulating the growth of human tumor cells in vitro.

2003-01-01

[Chem. Res. Toxicol. 16(1) , 48-55, (2003)]

LuxS: its role in central metabolism and the in vitro synthesis of 4-hydroxy-5-methyl-3(2H)-furanone.

2002-04-01

[Microbiology 148(Pt 4) , 909-22, (2002)]

More Articles...