Organic Letters 2003-10-02

Total synthesis of 10-norparvulenone and of O-methylasparvenone using a xanthate-mediated free radical addition-cyclization sequence.

Alejandro Cordero Vargas, Béatrice Quiclet-Sire, Samir Z Zard

Index: Org. Lett. 5(20) , 3717-9, (2003)

Full Text: HTML

Abstract

[reaction: see text] A short synthesis of (+/-)-10-norparvulenone and (+/-)-O-methylasparvenone was developed starting from commercially available m-methoxyphenol, hinging on a xanthate-mediated addition-cyclization sequence for the construction of the alpha-tetralone subunit.


Related Compounds

  • m-Methoxyphenol

Related Articles:

Convenient QSAR model for predicting the complexation of structurally diverse compounds with β-cyclodextrins

2009-01-01

[Bioorg. Med. Chem. 17 , 896-904, (2009)]

Calculating virtual log P in the alkane/water system (log P(N)(alk)) and its derived parameters deltalog P(N)(oct-alk) and log D(pH)(alk).

2005-05-05

[J. Med. Chem. 48 , 3269-79, (2005)]

Cellular apoptosis and cytotoxicity of phenolic compounds: a quantitative structure-activity relationship study.

2005-11-17

[J. Med. Chem. 48 , 7234-42, (2005)]

Action mechanism of tyrosinase on meta- and para-hydroxylated monophenols.

2000-04-01

[Biol. Chem. 381(4) , 313-20, (2000)]

Isolation and characterization of a veratrol:corrinoid protein methyl transferase from Acetobacterium dehalogenans.

2001-05-01

[Arch. Microbiol. 175(5) , 376-83, (2001)]

More Articles...