Preferential Bond Activation of sp3C–H over sp2C–H inα,β-Unsaturated Carboxylic Acids by Ruthenium Complex

2001 ◽  
Vol 30 (12) ◽  
pp. 1284-1285 ◽  
Author(s):  
Susumu Kanaya ◽  
Nobuyuki Komine ◽  
Masafumi Hirano ◽  
Sanshiro Komiya
Keyword(s):  
Carboxylic Acids ◽  
Bond Activation ◽  
Ruthenium Complex ◽  
Unsaturated Carboxylic Acids

Nickel-Catalyzed sp3 C–H Bond Activation from Decarboxylative Cross­Coupling of α,β-Unsaturated Carboxylic Acids with Amides

Synlett ◽  
2014 ◽  
Vol 25 (11) ◽  
pp. 1621-1625 ◽  
Author(s):  
Nai-Xing Wang ◽  
Jia-Xiang Zhang ◽  
Yan-Jing Wang ◽  
Wei Zhang ◽  
Cui-Bing Bai ◽  
...  
Keyword(s):  
Carboxylic Acids ◽  
Bond Activation ◽  
Unsaturated Carboxylic Acids

ChemInform Abstract: Nickel-Catalyzed sp3C-H Bond Activation from Decarboxylative Cross-Coupling of α,β-Unsaturated Carboxylic Acids with Amides.

ChemInform ◽  
2014 ◽  
Vol 45 (52) ◽  
pp. no-no
Author(s):  
Jia-Xiang Zhang ◽  
Yan-Jing Wang ◽  
Nai-Xing Wang ◽  
Wei Zhang ◽  
Cui-Bing Bai ◽  
...  
Keyword(s):  
Carboxylic Acids ◽  
Bond Activation ◽  
Cross Coupling ◽  
Unsaturated Carboxylic Acids

Perturbation theory of substituent effect. Importance of the field effect in transmission of the substituent effect

1980 ◽  
Vol 45 (6) ◽  
pp. 1655-1661 ◽  
Author(s):  
Robert Ponec
Keyword(s):  
Perturbation Theory ◽  
Carboxylic Acids ◽  
Quantum Chemical ◽  
Substituent Effect ◽  
Field Effect ◽  
Adequate Description ◽  
Meta Position ◽  
Unsaturated Carboxylic Acids

Various quantum chemical approaches to the problem of transmission of the substituent effect were compared. It was shown that inclusion of the electronic repulsion (field effect) was necessary to give a true picture of differences in ρ constants for reactions of the cis and trans isomers of substituted unsaturated carboxylic acids; the same holds for an adequate description of transmission of the substituent effect from the meta position on a given skeleton.

scholarly journals A solvent-dependent chirality-switchable thia-Michael addition to α,β-unsaturated carboxylic acids using a chiral multifunctional thiourea catalyst

2020 ◽  
Vol 11 (21) ◽  
pp. 5572-5576 ◽  
Author(s):  
Noboru Hayama ◽  
Yusuke Kobayashi ◽  
Eriko Sekimoto ◽  
Anna Miyazaki ◽  
Kiyofumi Inamoto ◽  
...  
Keyword(s):  
Carboxylic Acids ◽  
Tertiary Amine ◽  
Michael Addition ◽  
Arylboronic Acid ◽  
Unsaturated Carboxylic Acids

An asymmetric thia-Michael addition of arylthiols to α,β-unsaturated carboxylic acids using a thiourea catalyst that bears arylboronic acid and tertiary amine moieties is reported.

Nickel-Catalyzed Decarboxylative Difluoroalkylation of α,β-Unsaturated Carboxylic Acids

2016 ◽  
Vol 55 (10) ◽  
pp. 3491-3495 ◽  
Author(s):  
Gang Li ◽  
Tao Wang ◽  
Fan Fei ◽  
Yi-Ming Su ◽  
Yan Li ◽  
...  
Keyword(s):  
Carboxylic Acids ◽  
Unsaturated Carboxylic Acids
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