Tetra-primer ARMS PCR for rapid detection and characterisation ofPlasmopara viticolaphenotypes resistant to carboxylic acid amide fungicides

Hao Zhang; Fanfang Kong; Xina Wang; Lisha Liang; Cor D Schoen; Jie Feng; Zhongyue Wang

doi:10.1002/ps.4506

Tetra-primer ARMS PCR for rapid detection and characterisation ofPlasmopara viticolaphenotypes resistant to carboxylic acid amide fungicides

Pest Management Science ◽

10.1002/ps.4506 ◽

2017 ◽

Vol 73 (8) ◽

pp. 1655-1660 ◽

Cited By ~ 5

Author(s):

Hao Zhang ◽

Fanfang Kong ◽

Xina Wang ◽

Lisha Liang ◽

Cor D Schoen ◽

...

Keyword(s):

Carboxylic Acid ◽

Rapid Detection ◽

Acid Amide ◽

Carboxylic Acid Amide ◽

Arms Pcr

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Method for rapid detection of the PvCesA3 gene allele conferring resistance to mandipropamid, a carboxylic acid amide fungicide, in Plasmopara viticola populations

Pest Management Science ◽

10.1002/ps.2214 ◽

2011 ◽

Vol 67 (12) ◽

pp. 1557-1561 ◽

Cited By ~ 16

Author(s):

Yoshinao Aoki ◽

Seiichi Furuya ◽

Shunji Suzuki

Keyword(s):

Carboxylic Acid ◽

Rapid Detection ◽

Acid Amide ◽

Plasmopara Viticola ◽

Carboxylic Acid Amide

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QSAR Study on a Series of Aryl Carboxylic Acid Amide Derivatives as Potential Inhibitors of Dihydroorotate Dehydrogenase (DHODH)

Medicinal Chemistry ◽

10.2174/1573406411309020007 ◽

2013 ◽

Vol 9 (2) ◽

pp. 222-239 ◽

Cited By ~ 3

Author(s):

Vivek K. Vyas ◽

Manjunath Ghate

Keyword(s):

Carboxylic Acid ◽

Acid Amide ◽

Dihydroorotate Dehydrogenase ◽

Carboxylic Acid Amide ◽

Qsar Study ◽

Amide Derivatives ◽

Potential Inhibitors

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Discovery of 1-[9-(4-Chlorophenyl)-8-(2-chlorophenyl)-9H-purin-6-yl]-4-ethylaminopiperidine-4-carboxylic Acid Amide Hydrochloride (CP-945,598), a Novel, Potent, and Selective Cannabinoid Type 1 Receptor Antagonist

Journal of Medicinal Chemistry ◽

10.1021/jm8012932 ◽

2009 ◽

Vol 52 (2) ◽

pp. 234-237 ◽

Cited By ~ 51

Author(s):

David A. Griffith ◽

John R. Hadcock ◽

Shawn C. Black ◽

Philip A. Iredale ◽

Philip A. Carpino ◽

...

Keyword(s):

Carboxylic Acid ◽

Receptor Antagonist ◽

Acid Amide ◽

Carboxylic Acid Amide ◽

Cannabinoid Type 1 Receptor

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Carboxylic Acid Amide Fungicides for the Control of Downy Mildew Diseases

Bioactive Carboxylic Compound Classes: Pharmaceuticals and Agrochemicals ◽

10.1002/9783527693931.ch30 ◽

2016 ◽

pp. 395-403 ◽

Cited By ~ 1

Author(s):

Clemens Lamberth

Keyword(s):

Carboxylic Acid ◽

Downy Mildew ◽

Acid Amide ◽

Carboxylic Acid Amide

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Reaction of Indole Carboxylic Acid/Amide with Propargyl Alcohols: [4 + 3]-Annulation, Unexpected 3- to 2- Carboxylate/Amide Migration, and Decarboxylative Cyclization

Organic Letters ◽

10.1021/acs.orglett.9b01686 ◽

2019 ◽

Vol 21 (14) ◽

pp. 5447-5451 ◽

Cited By ~ 10

Author(s):

Karuppu Selvaraj ◽

Shubham Debnath ◽

K. C. Kumara Swamy

Keyword(s):

Carboxylic Acid ◽

Acid Amide ◽

Carboxylic Acid Amide ◽

Indole Carboxylic Acid ◽

Decarboxylative Cyclization ◽

Propargyl Alcohols

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Parallel Iterative Solution-Phase Synthesis of 5-Amino-1-aryl-[1,2,4]triazolo[1,5-a]pyridine-7-carboxylic Acid Amide Derivatives.

ChemInform ◽

10.1002/chin.200320170 ◽

2003 ◽

Vol 34 (20) ◽

Author(s):

Bernd Brodbeck ◽

Bernd Puellmann ◽

Sebastien Schmitt ◽

Matthias Nettekoven

Keyword(s):

Carboxylic Acid ◽

Acid Amide ◽

Iterative Solution ◽

Solution Phase ◽

Carboxylic Acid Amide ◽

Phase Synthesis ◽

Amide Derivatives ◽

Solution Phase Synthesis ◽

Parallel Iterative

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Rhodium catalyzed one-step hydroamidation of cyclopentadiene and dicyclopentadiene

Catalysis Science & Technology ◽

10.1039/c5cy00168d ◽

2015 ◽

Vol 5 (5) ◽

pp. 2783-2787 ◽

Cited By ~ 8

Author(s):

Arno Behr ◽

Denys Levikov ◽

Edward Nürenberg

Keyword(s):

Carboxylic Acid ◽

Acid Amide ◽

Amide Group ◽

Carboxylic Acid Amide ◽

Direct Route ◽

One Step ◽

Pharmaceutical Industries

The carboxylic acid amide group is of great importance in the contemporary chemical and pharmaceutical industries. A one-step rhodium catalyzed direct route from alkene to amide is presented via the hydroamidation reaction of cyclopentadiene and dicyclopentadiene.

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Solvent- and catalyst-free, quantitative protection of hydroxyl, thiol, carboxylic acid, amide and heterocyclic amino functional groups

Green Chemistry ◽

10.1039/c6gc02562e ◽

2016 ◽

Vol 18 (23) ◽

pp. 6209-6214 ◽

Cited By ~ 3

Author(s):

Mia L. Jawor ◽

Basil M. Ahmed ◽

Gellert Mezei

Keyword(s):

Carboxylic Acid ◽

Functional Groups ◽

Acid Amide ◽

Waste Materials ◽

Carboxylic Acid Amide ◽

Catalyst Free

Various substrates are quantitatively protected by 3,4-dihydro-2H-pyran at 125 °C in the absence of any additional chemicals, without generating any waste materials.

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