Applied Catalysis A: General

Bifunctional acid–base ionic liquid for the one-pot synthesis of fine chemicals: Thioethers, 2H-chromenes and 2H-quinoline derivatives

MJ Climent, S Iborra, MJ Sabater, JD Vidal

Index: Climent, Maria J.; Iborra, Sara; Sabater, Maria J.; Vidal, Juan D. Applied Catalysis A: General, 2014 , vol. 481, p. 27 - 38

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Citation Number: 4

Abstract

Abstract A bifunctional organocatalyst with ionic liquid properties and with an optimized distance between the acid and basic sites efficiently activates electron deficient olefins for 1, 4 conjugated addition, which can be incorporated in different one-pot transformations for the preparation of cyclic and acyclic compounds of biological and synthetic interest.

Mild Hydrosulfenylation of Olefins under Neutral Conditions Using a Defined NHC-Ligated Iron–Sulfur Catalyst

[Alt, Isabel; Rohse, Philipp; Plietker, Bernd ACS Catalysis, 2013 , vol. 3, # 12 p. 3002 - 3005]

Thia-michael addition reactions using 2-[bis (alkylthio) methylene]-3-oxo-No-tolylbutanamides as odorless and efficient thiol equivalents

[Dong, Dewen; Yu, Haifeng; Ouyang, Yan; Liu, Qun; Bi, Xihe; Lu, Yumei Synlett, 2006 , # 2 p. 283 - 287]

A mild and highly efficient one-pot three-component reaction for carbon–sulfur bond formation catalyzed by potassium tert-butoxide

[Movassagh, Barahman; Rakhshani, Amir Chinese Chemical Letters, 2011 , vol. 22, # 10 p. 1179 - 1182]