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  4. (ω-1)-Fluoroalk-(ω-1)-enoic Acids: Potential Fungicides
 
research article

(ω-1)-Fluoroalk-(ω-1)-enoic Acids: Potential Fungicides

Michel, Dominique
•
Schlosser, Manfred  
1996
Synthesis: Journal of Synthetic Organic Chemistry

(w - 1)-Fluoroalk-(w - 1)-enoic acids of chain lengths C5-C15 were prepd. by consecutive bromofluorination and dehydrobromination of either alk-(w - 1)-enoic acids or alk-(w - 1)-enyl acetates, in the latter case followed by oxidn. The halogen increases the antimyotic properties of the unsatd. fatty acids, 10-fluoroundec-10-enoic acid exhibiting a particularly strong fungicidal activity. [on SciFinder (R)]

  • Details
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Type
research article
DOI
10.1055/s-1996-4441
Author(s)
Michel, Dominique
Schlosser, Manfred  
Date Issued

1996

Publisher

Georg Thieme Verlag

Published in
Synthesis: Journal of Synthetic Organic Chemistry
Issue

8

Start page

1007

End page

1011

Subjects

Fungicides and Fungistats (prepn. of fluoroalkenoic acids as fungicides); Carboxylic acids Role: RCT (Reactant)

•

SPN (Synthetic preparation)

•

PREP (Preparation)

•

RACT (Reactant or reagent) (unsatd.

•

fluoro; prepn. of fluoroalkenoic acids as fungicides)

•

fluoroalkenoate fungicide prepn; carboxylate unsatd fluoro fungicide prepn

Note

CAN 125:194973

23-16

Aliphatic Compounds

Inst. Chim. Organique,Univ. Lausanne,Lausanne,Switz.

Journal

written in English.

180748-86-1P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of); 1786-40-9P; 175400-10-9P; 180748-68-9P; 180748-71-4P; 180748-72-5P; 180748-73-6P; 180748-74-7P; 180748-75-8P; 180748-76-9P; 180748-77-0P; 180748-78-1P; 180748-79-2P; 180748-80-5P; 180748-81-6P; 180748-85-0P Role: BAC (Biological activity or effector, except adverse), BSU (Biological study, unclassified), SPN (Synthetic preparation), BIOL (Biological study), PREP (Preparation) (prepn. of fluoroalkenoic acids as fungicides); 112-38-9 (10-Undecenoic acid); 1119-60-4 (6-Heptenoic acid); 1576-85-8 (4-Pentenyl acetate); 5048-26-0 (5-Hexenyl acetate); 6006-06-0 (12-Tridecenoic acid); 13826-35-2 (3-Phenoxybenzyl alcohol); 14436-32-9 (9-Decenoic acid); 17351-34-7 (14-Pentadecenoic acid); 18719-24-9 (7-Octenoic acid); 31642-67-8 (8-Nonenoic acid); 65423-25-8 (11-Dodecenoic acid); 68359-59-1 (2-Fluoro-5-phenoxybenzyl alcohol) Role: RCT (Reactant), RACT (Reactant or reagent) (prepn. of fluoroalkenoic acids as fungicides); 177089-58-6P; 177089-59-7P; 177089-60-0P; 180748-60-1P; 180748-61-2P; 180748-62-3P; 180748-63-4P; 180748-64-5P; 180748-65-6P; 180748-66-7P; 180748-67-8P; 180748-69-0P; 180748-70-3P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. of fluoroalkenoic acids as fungicides); 175399-95-8P; 175399-96-9P; 180748-82-7P; 180748-83-8P; 180748-84-9P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of fluoroalkenoic acids as fungicides)

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/20.500.14299/226928
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