Stereochemistry of nucleophilic addition reactions. Addition of diethyl malonate to ethyl 4-tert-butylcyclohexene-1-carboxylate. Equilibration of 1-tert-butyl-3-carboxymethylcyclohexane-4-carboxylic acids

1975 ◽  
Vol 40 (1) ◽  
pp. 34-41 ◽  
Author(s):  
Rudolph A. Abramovitch ◽  
Sandra S. Singer ◽  
Milorad M. Rogic ◽  
D. L. Struble
Keyword(s):  
Carboxylic Acids ◽  
Nucleophilic Addition ◽  
Diethyl Malonate ◽  
Addition Reactions ◽  
Tert Butyl

Stereochemistry of nucleophilic addition reactions. Addition of thiophenol and of hydrogen chloride to 4-tert-butyl-1-cyanocyclohexene

1972 ◽  
Vol 37 (23) ◽  
pp. 3577-3584 ◽  
Author(s):  
R. A. Abramovitch ◽  
Milorad M. Rogic ◽  
Sandra S. Singer ◽  
N. Venkateswaran
Keyword(s):  
Hydrogen Chloride ◽  
Nucleophilic Addition ◽  
Addition Reactions ◽  
Tert Butyl

scholarly journals Nucleophilic Addition Reactions of Nitriles to Nitrones under Mild Silylation Conditions

Synlett ◽  
2014 ◽  
Vol 25 (13) ◽  
pp. 1863-1868 ◽  
Author(s):  
Fumihiko Yoshimura ◽  
Keiji Tanino ◽  
Taiki Abe
Keyword(s):  
Nucleophilic Addition ◽  
Addition Reactions

ChemInform Abstract: The Interaction of 3,5-Di-tert-butyl-4-hydroxybenzylacetate with Salts of Carboxylic Acids. The Synthesis of Bis(3,5-di-tert-butyl-4- hydroxybenzylic) Ether.

ChemInform ◽  
2010 ◽  
Vol 27 (7) ◽  
pp. no-no
Author(s):  
S. V. BUKHAROV ◽  
V. D. NUSINOVICH ◽  
YU. V. CHUGUNOV ◽  
YU. YA. EFREMOV ◽  
YA. D. SAMUILOV
Keyword(s):  
Carboxylic Acids ◽  
Tert Butyl

Amide-Directed Reactions of Small Carbocycles

2021 ◽  
Vol 25 ◽  
Author(s):  
Pavel M. Yamanushkin ◽  
Marina Rubina ◽  
Michael Rubin
Keyword(s):  
Transition Metal ◽  
Transition Metals ◽  
Nucleophilic Addition ◽  
Addition Reactions ◽  
Transition Metal Catalyzed ◽  
Metal Catalyzed

: The topic of this review is the amide-directed functionalization of strained carbocycles — specifically, unsaturated or saturated three- and four-membered rings. The following approaches are discussed: a) directed carbometallation and hydrometallation of cyclopropenes catalyzed by transition metals; b) directed metal-templated nucleophilic addition reactions; c) directed C-H functionalization, including transition metal-catalyzed C-H-activation reactions; and d) directed radical additions.

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