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 Control of Chemoselectivity in Dirhodium(II)-Catalyzed Reaction of 5,6-Dioxygenated 2-Diazo-3-oxohexanoates: C-H Insertion Reaction versus Oxonium Ylide Formation.

1998 ◽  
Vol 46 (7) ◽  
pp. 1182-1183 ◽  
Author(s):  
Takayuki YAKURA ◽  
Akiharu UEKI ◽  
Yukiko MORIOKA ◽  
Toyoshige KURATA ◽  
Kenji TANAKA ◽  
...  
Keyword(s):  
Insertion Reaction ◽  
Oxonium Ylide

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

Trapping of Oxonium Ylide with Isatins:  Efficient and Stereoselective Construction of Adjacent Quaternary Carbon Centers

2007 ◽  
Vol 9 (23) ◽  
pp. 4721-4723 ◽  
Author(s):  
Xin Guo ◽  
Haoxi Huang ◽  
Liping Yang ◽  
Wenhao Hu
Keyword(s):  
Quaternary Carbon ◽  
Carbon Centers ◽  
Oxonium Ylide

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
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