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  4. Attempted and accomplished syntheses of a few monofluorinated chrysanthemic acid derivatives
 
research article

Attempted and accomplished syntheses of a few monofluorinated chrysanthemic acid derivatives

Cottens, Sylvain
•
Schlosser, Manfred  
1988
Tetrahedron

A sulfone mediated approach presumably did produce Me a-fluorochrysanthemate I but, if formed, the latter immediately underwent dehydrofluorination under the strongly basic reaction conditions. The cis- and trans-isomers of Me b- and g-fluorochysanthemates II and III were concomitantly obtained by treating 3-fluoro-2,5-dimethyl-2,4-hexadiene with N2CH2CO2Me in the presence of catalytic amts. of Rh(OAc)2. After enzymic and chromatog. sepn. the four individual components were converted to the m-phenoxybenzyl esters. [on SciFinder (R)]

  • Details
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Type
research article
DOI
10.1016/S0040-4020(01)86081-6
Author(s)
Cottens, Sylvain
Schlosser, Manfred  
Date Issued

1988

Published in
Tetrahedron
Volume

44

Issue

23

Start page

7127

End page

44

Subjects

Pyrethrins and Pyrethroids Role: RCT (Reactant)

•

RACT (Reactant or reagent) (fluorochrysanthic acids esters)

•

fluorochrysanthemic acid deriv prepn; fluorodimethylhexadiene cyclopropantion diazoacetate rhodium catalyst; phenoxybenzyl fluorochrysanthemate

Note

CAN 111:214709

30-10

Terpenes and Terpenoids

Inst. Chim. Org.,Univ. Lausanne,Lausanne,Switz.

Journal

written in English.

63995-82-4 (2-Fluoro-3-methyl-2-butenal) Role: RCT (Reactant), RACT (Reactant or reagent) (carbonyl oxidn. or Wittig reactions of); 15543-64-3 Role: RCT (Reactant), RACT (Reactant or reagent) (condensation of, with fluorobutenoate); 764-13-6 (2,5-Dimethyl-2,4-hexadiene) Role: RCT (Reactant), RACT (Reactant or reagent) (cyclopropenation and competition expts. of, vs. its fluoro derivs.); 82147-66-8P (Methyl 2-fluoro-3-methyl-2-butenoate) Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. and condensation of, with butenyl tolyl sulfone); 123502-19-2P; 123502-20-5P; 123502-21-6P; 123502-22-7P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and esterification of); 123502-15-8P; 123502-16-9P; 123502-17-0P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and hydrolysis of); 76827-57-1P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and reaction of, with diazoacetate); 95887-29-9P; 123502-01-2P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and reactions of, with diazoacetates); 123502-03-4P; 123502-04-5P; 123502-06-7P; 123502-07-8P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and transesterification of); 4638-92-0DP; 123502-00-1P; 123502-02-3P; 123502-05-6P; 123502-09-0P; 123502-10-3P; 123502-18-1P; 123521-96-0P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of); 123502-08-9P; 123502-11-4P; 123502-12-5P; 123502-13-6P; 123539-92-4P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of, as potential pyrethroid); 123502-23-8P; 123502-24-9P; 123502-25-0P; 123502-26-1P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of, as potential pyrethroids); 123502-14-7P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn., ring cleavage, and hydrolysis of); 76-09-5 (Pinacol) Role: RCT (Reactant), RACT (Reactant or reagent) (reaction of, with chlorofluoromethoxycyclopropane); 123501-99-5 Role: RCT (Reactant), RACT (Reactant or reagent) (ring opening reactions of); 13826-35-2 Role: RCT (Reactant), RACT (Reactant or reagent) (transesterification by, of fluorochrysanthemate Me esters)

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LSCO  
Available on Infoscience
March 3, 2006
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/226843
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