NEW DECARBOXYLATIVE SULFANYLATION OF SOME PHENYLSULFONYL ARYLACETIC ACIDS

2000 ◽  
Vol 161 (1) ◽  
pp. 1-7 ◽  
Author(s):  
Blanka Wladislaw ◽  
Liliana Marzorati ◽  
Claudio Di Vitta ◽  
Nelson F. Claro
Keyword(s):  
Arylacetic Acids

scholarly journals Dirhodium Carboxylate Catalysts from 2‐Fenchyloxy or 2‐Menthyloxy Arylacetic Acids: Enantioselective C−H Insertion, Aromatic Addition and Oxonium Ylide Formation/Rearrangement

ChemCatChem ◽  
2021 ◽  
Author(s):  
Aoife M. Buckley ◽  
Daniel C. Crowley ◽  
Thomas A. Brouder ◽  
Alan Ford ◽  
U. B. Rao Khandavilli ◽  
...  
Keyword(s):  
Arylacetic Acids ◽  
Oxonium Ylide

Elemental Sulfur Mediated Decarboxylative Redox Cyclization Reaction of o-Chloronitroarenes and Arylacetic Acids

2015 ◽  
Vol 17 (4) ◽  
pp. 976-978 ◽  
Author(s):  
Tirumaleswararao Guntreddi ◽  
Rajeshwer Vanjari ◽  
Krishna Nand Singh
Keyword(s):  
Elemental Sulfur ◽  
Cyclization Reaction ◽  
Arylacetic Acids

scholarly journals Metal Ion Oxidation. IX. Oxidation of Aromatic Hydrocarbons and Arylacetic Acids by Heteropoly Anions Containing Ni(IV), Mn(IV) and Co(III) Ions as Central Atoms.

1983 ◽  
Vol 37b ◽  
pp. 761-768 ◽  
Author(s):  
Lennart Jönsson ◽  
Ghazi Noori ◽  
Rolf Bergman ◽  
Ewa Kesler ◽  
Olov Sterner ◽  
...  
Keyword(s):  
Aromatic Hydrocarbons ◽  
Metal Ion ◽  
Arylacetic Acids

One-Pot Access to 4-Aryl-2-arylacetoxynaphthalenes via Benz­annulation of Oxygenated Arylacetic Acids and Alkyl Aryl Ketones

Synthesis ◽  
2020 ◽  
Vol 52 (07) ◽  
pp. 1035-1046 ◽  
Author(s):  
Meng-Yang Chang ◽  
Shin-Mei Chen ◽  
Yu-Ting Hsiao
Keyword(s):  
Bond Formation ◽  
Trifluoroacetic Anhydride ◽  
Ring Closure ◽  
One Pot ◽  
Alkyl Aryl ◽  
Highly Effective ◽  
Aryl Ketones ◽  
Arylacetic Acids ◽  
Plausible Mechanism

Trifluoroacetic anhydride mediated one-pot intermolecular formal (4+2) benzannulation of oxygenated arylacetic acids with alkyl aryl ketones provides 4-aryl-2-arylacetoxynaphthalenes in moderate to good yields in the presence of H3PO4 in an open-vessel in a straightforward procedure. A plausible mechanism is proposed and discussed. This protocol provides a highly effective ring-closure via two carbon–carbon (C–C) and one carbon–oxygen (C–O) bond-formation events.

Arylacetic Acids in Organic Synthesis

2019 ◽  
Vol 9 (1) ◽  
pp. 23-41 ◽  
Author(s):  
Chenxi Yang ◽  
Xia Sheng ◽  
Ling Zhang ◽  
Jiang Yu ◽  
Dayun Huang
Keyword(s):  
Organic Synthesis ◽  
Arylacetic Acids

scholarly journals CuO-catalyzed conversion of arylacetic acids into aromatic nitriles with K4Fe(CN)6 as the nitrogen source

2021 ◽  
Vol 149 ◽  
pp. 106175
Author(s):  
Ai-Ping Xing ◽  
Zhenpeng Shen ◽  
Zhe Zhao ◽  
Xinzhe Tian ◽  
Yun-Lai Ren
Keyword(s):  
Nitrogen Source ◽  
Aromatic Nitriles ◽  
Arylacetic Acids

scholarly journals Functionalization of C–H bonds in acetophenone oximes with arylacetic acids and elemental sulfur

RSC Advances ◽  
2020 ◽  
Vol 10 (19) ◽  
pp. 11024-11032 ◽  
Author(s):  
Phuc H. Pham ◽  
Khang X. Nguyen ◽  
Hoai T. B. Pham ◽  
Thien T. Tran ◽  
Tung T. Nguyen ◽  
...  
Keyword(s):  
Transition Metals ◽  
Elemental Sulfur ◽  
Arylacetic Acids ◽  
Acetophenone Oxime

Annulation of acetophenone oxime acetates, arylacetic acids or esters, and elemental sulfur in absence of transition metals is reported.

Cu(i)/{Nb6O19} catalyzed N-acylation of arylacetic acids with amines under aerobic conditions

2018 ◽  
Vol 54 (88) ◽  
pp. 12471-12474 ◽  
Author(s):  
Pei-He Li ◽  
Zheng Wang ◽  
Hui Fu ◽  
Qi-Pu Dai ◽  
Chang-Wen Hu
Keyword(s):  
Catalyst System ◽  
Aerobic Conditions ◽  
Arylacetic Acids

Employing a simple copper(i)/{Nb6O19} catalyst system, the reaction reported herein offers a facile process to give functionalized α-ketoamides from readily available arylacetic acids under aerobic conditions.

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