European Journal of Organic Chemistry 2017-10-09

Directing the Cation Recognition Ability of Calix[4]arenes toward Asymmetric Phase-Transfer Catalysis

Nicola Alessandro De Simone, Rosaria Schettini, Carmen Talotta, Carmine Gaeta, Irene Izzo, Giorgio Della Sala, Placido Neri

Index: 10.1002/ejoc.201700912

Full Text: HTML

Abstract

The recognition abilities of chiral calixarene hosts toward alkali cation guests have been exploited for the first time in asymmetric phase-transfer (PT) catalysis. The binding affinities of a series of α-methylbenzylamine-derived calix[4]arene-amides toward Na+ are consistent with their catalytic efficiency in the asymmetric alkylation of N-(diphenylmethylene)glycine esters under PT conditions.

Latest Articles:

Development of Photoactivatable Nitroxyl (HNO) Donors Incorporating the (3‐Hydroxy‐2‐naphthalenyl)methyl Phototrigger

2018-04-15

[10.1002/ejoc.201800092]

Catalytic C‐Alkylation of Pyrroles with Primary Alcohols: Hans Fischer's Alkali and a New Method with Iridium P,N,P‐Pincer Complexes

2018-03-30

[10.1002/ejoc.201800146]

Fluorine‐Containing Functionalized Cyclopentene Scaffolds Through Ring Contraction and Deoxofluorination of Various Substituted Cyclohexenes

2018-03-30

[10.1002/ejoc.201800057]

Verdazyl Radical Building Blocks: Synthesis, Structure, and Sonogashira Cross‐Coupling Reactions

2018-03-30

[10.1002/ejoc.201701783]

Iron‐Catalyzed Sulfur‐Promoted Decyanative Redox Condensation of o‐Nitrophenols and Arylacetonitriles: An Unprecedented Route to 2‐Arylbenzoxazoles

2018-03-30

[10.1002/ejoc.201701607]

More Articles...