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research article

Total synthesis of 3,3'-biflavone

Zhu, Jieping  
•
Wang, Qian  
•
Li, Yulin
1988
Journal of the Chemical Society, Chemical Communications

3,3'-Biflavones I (R = H, OMe) were prepd. from phloroglucinol via Baker-Venkataraman rearrangement of the diesters II (R1 = COC6H4R-4) and cyclization. [on SciFinder (R)]

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Type
research article
DOI
10.1039/C39880001549
Author(s)
Zhu, Jieping  
Wang, Qian  
Li, Yulin
Date Issued

1988

Published in
Journal of the Chemical Society, Chemical Communications
Issue

23

Start page

1549

End page

1550

Subjects

biflavone

Note

CAN 110:212429

26-4

Biomolecules and Their Synthetic Analogs

Inst. Org. Chem.,Lanzhou Univ.,Lanzhou,Peop. Rep. China.

Journal

written in English.

543-20-4 (Succinoyl chloride) Role: RCT (Reactant), RACT (Reactant or reagent) (Friedel-Crafts reaction of, with phloroglucinol tri-Me ether); 108-73-6 (Phloroglucinol) Role: RCT (Reactant), RACT (Reactant or reagent) (methylation of); 120341-53-9P; 120341-54-0P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and Baker-Venkataraman rearrangement of); 621-23-8P (Phloroglucinol trimethyl ether) Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and Friedel-Crafts reaction of, with succinoyl chloride); 120341-55-1P; 120527-70-0P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and cyclization of); 120341-52-8P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and esterification of); 120341-51-7P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and selective demethylation of); 20081-63-4P; 120341-56-2P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of)

Editorial or Peer reviewed

REVIEWED

Written at

OTHER

EPFL units
LSPN  
Available on Infoscience
November 25, 2010
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/58590
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