## Abstract ( ± )‐5,5″‐Dihydroxy‐7,7″‐dimethoxy‐8,8″‐biflavone (( ± )‐l) was resolved into its optically pare forms __via__ the formation and recrystallization of its (2__R__)‐ and (2__S__)‐1‐(4‐toluenesulfonyl)prolylate, and the methylated derivatives of (+)‐ and (‐)‐1 were also prepared. The abso
The first enantioselective synthesis of optically pure (R)- and (S)-5,5″-dihydroxy-4′,4‴,7,7″-tetramethoxy-8,8″-biflavone and the reconfirmation of their absolute configuration
✍ Scribed by Guo-Qiang Lin; Min Zhong
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 220 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
The first enantioselective synthesis of the optically pure (R)-and (S) -5,5"-dihydroxy-4',4'",7,7"-tetramethoxy -8,8"-bitlavone is described. The key steps involve the intramolecular oxidative coupling of the cyanocuprat¢ intermediate and FriedeI-Cmfls rearrangement. Their absolute configuration was reconfirmed by CD spectra.
📜 SIMILAR VOLUMES
## Abstract (4__R__,5__R__,6__S__,7__E__,9__E__)‐4,6,8‐Trimethyl‐7,9‐undecadien‐5‐ol (1) and its antipode 1′, the female specific compound of the woodroach __Cryptocercus punctulatus__, were synthesized by starting from methyl (__R__)‐3‐hydroxy‐2‐methylpropanoate (C).
9.111.90
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract By synthesizing some isomers of 4,6,8‐trimethyl‐7,9‐undeca‐dien‐5‐ol, (4__R__\*,5__R__\*,6__S__\*,7__E__,9__E__)‐relative stereochemistry was assigned to the isomer isolated as the female specific compound of the tergal glands secretion of the woodroach __Cryptocercus punctulatus__.