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  4. Synthesis of various substituted dibenzo[b,d]pyranones including amino acid derivatives by SRN1 methodology
 
research article

Synthesis of various substituted dibenzo[b,d]pyranones including amino acid derivatives by SRN1 methodology

Beugelmans, Rene
•
Bois-Choussy, Michele
•
Chastanet, Jacqueline
Show more
1993
Heterocycles

An easy prepn. of the title compds. involving a SRN1 o-arylation of phenolates by o-bromobenzonitrile followed by SiO2-catalyzed lactonization is described. Activated or not activated phenols are efficient. Access to benzonaphthopyranones is exemplified by the reactions with 2-naphtholate. Reactions with chiral p-hydroxyphenylamino acid derivs. are also reported. Thus, irradn. of Ac-L-Tyr(Ac)-OMe and 2-bromo-4,5-dimethoxybenzonitrile in liq. NH3, followed by treatment with silica in CH2Cl2, gave 52% dibenzopyranyl amino ester I. [on SciFinder (R)]

  • Details
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Type
research article
DOI
10.3987/COM-93-6494
Author(s)
Beugelmans, Rene
Bois-Choussy, Michele
Chastanet, Jacqueline
Le Gleuher, Martine
Zhu, Jieping  
Date Issued

1993

Published in
Heterocycles
Volume

36

Issue

12

Start page

2733

End page

32

Subjects

Amino acids Role: SPN (Synthetic preparation)

•

PREP (Preparation) (dibenzopyranyl

•

prepn. via nucleophilic radical arom substitution reactions of phenol derivs. with bromobenzonitriles and silica-catalyzed cyclization); Cyclocondensation reaction (nucleophilic radical arom substitution reactions and

•

of bromobenzonitriles with phenols and naphthols to dibenzopyranones); Phenols Role: RCT (Reactant)

•

RACT (Reactant or reagent) (nucleophilic radical arom substitution reactions with bromobenzonitriles and silica-catalyzed cyclization to dibenzopyranones); Substitution reaction (homolytic

•

of bromobenzonitriles with phenols and naphthols

•

and silica-catalyzed cyclization to dibenzopyranones)

•

nucleophilic radical arom substitution phenolate; lactonization cyanophenylphenol; phenol cyanophenyl lactonization; dibenzopyranone; amino acid dibenzopyranylmethyl

Note

CAN 120:245721

34-2

Amino Acids, Peptides, and Proteins

Inst. Chim. Subs. Nat.,CNRS,Gif-sur-Yvette,Fr.

Journal

written in English.

100-02-7 (4-Nitrophenol) Role: RCT (Reactant), RACT (Reactant or reagent) (attempted nucleophilic radical arom substitution reactions with bromobenzonitrile); 135-19-3 (2-Naphthol) Role: RCT (Reactant), RACT (Reactant or reagent) (nucleophilic radical arom substitution reactions with bromobenzonitriles); 96-76-4 (2,4-Di-tert-butylphenol); 98-54-4 (4-tert-Butylphenol); 371-41-5 (4-Fluorophenol); 767-00-0 (4-Hydroxybenzonitrile); 828-27-3 (4-(Trifluoromethoxy)phenol); 2033-89-8 (3,4-Dimethoxyphenol); 35068-04-3 (N,O-Diacetyltyrosine methyl ester); 143674-61-7 Role: RCT (Reactant), RACT (Reactant or reagent) (nucleophilic radical arom substitution reactions with bromobenzonitriles and silica-catalyzed cyclization to dibenzopyranones); 78247-62-8 Role: RCT (Reactant), RACT (Reactant or reagent) (nucleophilic radical arom substitution reactions with bromobenzonitriles and silica-catalyzed cyclization to dibenzopyranones, racemization in); 2042-37-7 (2-Bromobenzonitrile); 109305-98-8 (2-Bromo-4,5-dimethoxybenzonitrile) Role: RCT (Reactant), RACT (Reactant or reagent) (nucleophilic radical arom substitution reactions with phenol and naphthol derivs. and silica-catalyzed cyclization to dibenzopyranones); 154145-18-3P; 154145-19-4P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. and silica-catalyzed cyclization to dibenzopyranone); 100540-63-4P; 101438-97-5P (5H-Benzo[d]naphtho[2,1-b]pyran-5-one); 108012-00-6P; 151648-57-6P; 151648-58-7P; 151648-59-8P (5H-Benzo[d]naphtho[2,3-b]pyran-5-one); 154145-15-0P; 154145-16-1P; 154145-17-2P; 154145-20-7P; 154145-21-8P; 154145-22-9P; 154145-23-0P; 154145-24-1P; 154145-25-2P 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/20.500.14299/58576
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