A quaternary ammonium salt [H-dabco][AcO]: as a recyclable and highly efficient catalyst for the one-pot synthesis of β-phosphonomalonates

Ya-Qin Yu and Da-Zhen Xu

RSC Adv., 2015, 5, 28857
DOI: 10.1039/C5RA02743H

Design and synthesis of bistereogenic chiral ionic liquids and their use as solvents for asymmetric Baylis–Hillman reactions

Satish Garre, Erica Parker, Bukuo Ni and Allan D. Headley

Org. Biomol. Chem., 2008, 6, 3041
DOI: 10.1039/b808502a

Supported proline and proline-derivatives as recyclable organocatalysts

Michelangelo Gruttadauria, Francesco Giacalone and Renato Noto

Chem. Soc. Rev., 2008, 37, 1666
DOI: 10.1039/b800704g

Pyrrolidine modified PANF catalyst for asymmetric Michael addition of ketones to nitrostyrenes in aqueous phase

Jianguo Du, Bin Shuai, Minli Tao, Guangwei Wang and Wenqin Zhang

Green Chem., 2016, 18, 2625
DOI: 10.1039/C5GC02622A

Chiral ionic liquids derived from isosorbide: synthesis, properties and applications in asymmetric synthesis

Olivier Nguyen Van Buu, Audrey Aupoix, Nhung Doan Thi Hong and Giang Vo-Thanh

New J. Chem., 2009, 33, 2060
DOI: 10.1039/b902956g

Synthesis of γ-nitroaldehydes containing quaternary carbon in the α-position using a 4-oxalocrotonate tautomerase whole-cell biocatalyst

Jelena Radivojevic, Gordana Minovska, Lidija Senerovic, Kevin O'Connor, Predrag Jovanovic, Vladimir Savic, Zorana Tokic-Vujosevic, Jasmina Nikodinovic-Runic and Veselin Maslak

RSC Adv., 2014, 4, 60502
DOI: 10.1039/C4RA05517A

A chiral thioureido acid as an effective additive for enantioselective organocatalytic Michael additions of nitroolefins

Dan-Qian Xu, Hua-Dong Yue, Shu-Ping Luo, Ai-Bao Xia, Shuai Zhang and Zhen-Yuan Xu

Org. Biomol. Chem., 2008, 6, 2054
DOI: 10.1039/b804541k

Catalysts with ionic tag and their use in ionic liquids

Radovan Šebesta, Iveta Kmentová and Štefan Toma

Green Chem., 2008, 10, 484
DOI: 10.1039/b801456f

Coordinating chiral ionic liquids

Maria Vasiloiu, Sonja Leder, Peter Gaertner, Kurt Mereiter and Katharina Bica

Org. Biomol. Chem., 2013, 11, 8092
DOI: 10.1039/c3ob41635f

Ionic liquid [Dabco-H][AcO] as a highly efficient and recyclable catalyst for the synthesis of various bisenol derivatives via domino Knoevenagel–Michael reaction in aqueous media

Cheng Yang, Wan-Qi Su and Da-Zhen Xu

RSC Adv., 2016, 6, 99656
DOI: 10.1039/C6RA23018K

Imidazolium chiral ionic liquid derived carbene-catalyzed conjugate umpolung for synthesis of γ-butyrolactones

Feng-Li Yu, Jia-Jia Jiang, Dong-Mei Zhao, Cong-Xia Xie and Shi-Tao Yu

RSC Adv., 2013, 3, 3996
DOI: 10.1039/c3ra40211h

Highly efficient asymmetric Michael addition of aldehyde to nitroolefin using perhydroindolic acid as a chiral organocatalyst

Lina Zhao, Jiefeng Shen, Delong Liu, Yangang Liu and Wanbin Zhang

Org. Biomol. Chem., 2012, 10, 2840
DOI: 10.1039/c2ob00003b

Proline-based reduced dipeptides as recyclable and highly enantioselective organocatalysts for asymmetric Michael addition

Xiaohui Cao, Ge Wang, Richeng Zhang, Yingying Wei, Wei Wang, Huichao Sun and Ligong Chen

Org. Biomol. Chem., 2011, 9, 6487
DOI: 10.1039/c1ob05679d

A recyclable non-immobilized siloxy serine organocatalyst for the asymmetric direct aldol reaction

Yong-Chua Teo and Guan-Leong Chua

Tetrahedron Letters, 2008, 49, 4235
DOI: 10.1016/j.tetlet.2008.04.159

Multiple Catalysis with Two Chiral Units: An Additional Dimension for Asymmetric Synthesis

Susy Piovesana, Daniele M. Scarpino Schietroma and Marco Bella

Angew Chem Int Ed, 2011, 50, 6216
DOI: 10.1002/anie.201005955

Asymmetric SN1 α‐Alkylation of Cyclic Ketones Catalyzed by Functionalized Chiral Ionic Liquid (FCIL) Organocatalysts

Long Zhang, Lingyun Cui, Xin Li, Jiuyuan Li, Sanzhong Luo and Jin‐Pei Cheng

Chemistry A European J, 2010, 16, 2045
DOI: 10.1002/chem.200902509

Symmetry Breaking in Chiral Ionic Liquids Evidenced by Vibrational Optical Activity

Patric Oulevey, Sandra Luber, Birte Varnholt and Thomas Bürgi

Angew Chem Int Ed, 2016, 55, 11787
DOI: 10.1002/anie.201605792

“Nonsolvent” Applications of Ionic Liquids in Biotransformations and Organocatalysis

Pablo Domínguez de María

Angew Chem Int Ed, 2008, 47, 6960
DOI: 10.1002/anie.200703305

Metal-free methods for the generation of benzimidazoles and 2-aminobenzimidazoles

Pravin J. Wanjari, Nirjhar Saha, Gurudutt Dubey and Prasad V. Bharatam

Tetrahedron, 2023, 130, 133143
DOI: 10.1016/j.tet.2022.133143

Ionic Liquids: Synthesis and Applications in Catalysis

Rajni Ratti

Advances in Chemistry, 2014, 2014, 1
DOI: 10.1155/2014/729842

Asymmetrische Organokatalyse: Eintritt in die Reifezeit

Alessandro Dondoni and Alessandro Massi

Angewandte Chemie, 2008, 120, 4716
DOI: 10.1002/ange.200704684

Imidazolium-based chiral ionic liquids: synthesis and application

Yumiko Suzuki, Junichiro Wakatsuki, Mariko Tsubaki and Masayuki Sato

Tetrahedron, 2013, 69, 9690
DOI: 10.1016/j.tet.2013.09.017

Functionalized Chiral Ionic Liquid Catalyzed Asymmetric SN1 α‐Alkylation of Ketones and Aldehydes

Long Zhang, Lingyun Cui, Xin Li, Jiuyuan Li, Sanzhong Luo and Jin‐Pei Cheng

Eur J Org Chem, 2010, 2010, 4876
DOI: 10.1002/ejoc.201000609

Basic chiral ionic liquids: A novel strategy for acid-free organocatalysis

Maria Vasiloiu, Daniel Rainer, Peter Gaertner, Christian Reichel, Christian Schröder and Katharina Bica

Catalysis Today, 2013, 200, 80
DOI: 10.1016/j.cattod.2012.07.002

Chiral quaternary alkylammonium ionic liquid [Pro-dabco][BF4]: as a recyclable and highly efficient organocatalyst for asymmetric Michael addition reactions

Da-Zhen Xu, Yingjun Liu, Sen Shi and Yongmei Wang

Tetrahedron: Asymmetry, 2010, 21, 2530
DOI: 10.1016/j.tetasy.2010.10.009

Pyrrolidine-Based Chiral Quaternary Alkylammonium Ionic Liquids as Organocatalysts for Asymmetric Michael Additions

Ge Wang, Huichao Sun, Xiaohui Cao and Ligong Chen

Catal Lett, 2011, 141, 1324
DOI: 10.1007/s10562-011-0649-4

Ionic-liquid-supported 1,5,7-triazabicyclo[4.4.0]dec-5-ene — An efficient and recyclable organocatalyst for Michael addition to α,β-unsaturated ketones

Manoj Kumar Muthyala, Bhupender S Chhikara, Keykavous Parang and Anil Kumar

Can. J. Chem., 2012, 90, 290
DOI: 10.1139/v11-162

Installation of the imidazole ring on chiral substrates via allylic substitution

Yuichi Kobayashi, Yohei Kiyotsuka, Yusuke Sugihara and Kyohei Wada

Tetrahedron, 2015, 71, 6481
DOI: 10.1016/j.tet.2015.05.004

Asymmetric Michael Additions Catalysed by Functionalised Quaternary Alkylammonium Ionic Liquids

Ge Wang, Huichao Sun, Xiaohui Cao, Yang Li and Ligong Chen

Journal of Chemical Research, 2012, 36, 96
DOI: 10.3184/174751912X13280326501363

Highly efficient morpholine-based organocatalysts for the 1,4-addition reaction between aldehydes and nitroolefins: an unexploited class of catalysts

Francesco Vaghi, Giorgio Facchetti, Isabella Rimoldi, Matteo Bottiglieri, Alessandro Contini, Maria Luisa Gelmi and Raffaella Bucci

Front. Chem., 2023, 11
DOI: 10.3389/fchem.2023.1233097

Recent Developments on Supported Hydrogen‐bond Organocatalysts

Antonio Franconetti and Gonzalo de Gonzalo

ChemCatChem, 2018, 10, 5554
DOI: 10.1002/cctc.201801459

Asymmetric Organocatalysis: From Infancy to Adolescence

Alessandro Dondoni and Alessandro Massi

Angew Chem Int Ed, 2008, 47, 4638
DOI: 10.1002/anie.200704684

Synthesis and Antimicrobial Activity of Imidazolium and Triazolium Chiral Ionic Liquids

Paweł Borowiecki, Małgorzata Milner‐Krawczyk, Dominika Brzezińska, Monika Wielechowska and Jan Plenkiewicz

Eur J Org Chem, 2013, 2013, 712
DOI: 10.1002/ejoc.201201245

A mild and efficient procedure for asymmetric Michael additions of cyclohexanone to chalcones catalyzed by an amino acid ionic liquid

Yunbo Qian, Shiyong Xiao, Lei Liu and Yongmei Wang

Tetrahedron: Asymmetry, 2008, 19, 1515
DOI: 10.1016/j.tetasy.2008.06.022

Highly efficient and recoverable dendritic organocatalyst from click chemistry for the asymmetric michael addition of ketones to nitroolefins without the use of organic solvent

Guanghua Lv, Rizhe Jin, Wenpeng Mai and Lianxun Gao

Tetrahedron: Asymmetry, 2008, 19, 2568
DOI: 10.1016/j.tetasy.2008.10.016

Polymer‐Immobilized Pyrrolidine‐Based Chiral Ionic Liquids as Recyclable Organocatalysts for Asymmetric Michael Additions to Nitrostyrenes under Solvent‐Free Reaction Conditions

Pinhua Li, Lei Wang, Min Wang and Yicheng Zhang

Eur J Org Chem, 2008, 2008, 1157
DOI: 10.1002/ejoc.200701037

Highly Enantioselective Conjugate Addition of Ketones to Alkylidene Malonates Catalyzed by a Pyrrolidinyl–Camphor‐Derived Organocatalyst

Dhananjay R. Magar, Chihliang Chang, Ying‐Fang Ting and Kwunmin Chen

Eur J Org Chem, 2010, 2010, 2062
DOI: 10.1002/ejoc.201000072

Are Ionic Liquids Suitable Media for Organocatalytic Reactions?

Štefan Toma, Mária Mečiarová and Radovan Šebesta

Eur J Org Chem, 2009, 2009, 321
DOI: 10.1002/ejoc.200800809

Ionic Liquids in Asymmetric Synthesis: An Overall View from Reaction Media to Supported Ionic Liquid Catalysis

Babak Karimi, Mina Tavakolian, Maryam Akbari and Fariborz Mansouri

ChemCatChem, 2018, 10, 3173
DOI: 10.1002/cctc.201701919

The role of neutral anions in ionic liquid as solvent media for the reactivity and stereoselectivity towards asymmetric Michael addition reaction of n-pentanal with β-nitrostyrene catalyzed by L-Proline

Emmy M. Omar, Mohd Basyaruddin A. Rahman, Bukuo Ni and Allan D. Headley

Synthetic Communications, 2019, 49, 1578
DOI: 10.1080/00397911.2019.1604969

Acidic ionic liquid [NMP]H2PO4 as dual solvent-catalyst for synthesis of β-alkoxyketones by the oxa-Michael addition reactions

Hui Guo, Xia Li, Jun-Liang Wang, Xiao-Han Jin and Xian-Fu Lin

Tetrahedron, 2010, 66, 8300
DOI: 10.1016/j.tet.2010.08.017

Basic-functionalized recyclable ionic liquid catalyst: A solvent-free approach for Michael addition of 1,3-dicarbonyl compounds to nitroalkenes under ultrasound irradiation

Senthil Narayanaperumal, Rodrigo César da Silva, Karla Santos Feu, Alexander Fernández de la Torre, Arlene G. Corrêa and Márcio Weber Paixão

Ultrasonics Sonochemistry, 2013, 20, 793
DOI: 10.1016/j.ultsonch.2012.11.002

Chiral ionic liquids in chromatographic and electrophoretic separations

Constantina P. Kapnissi-Christodoulou, Ioannis J. Stavrou and Maria C. Mavroudi

Journal of Chromatography A, 2014, 1363, 2
DOI: 10.1016/j.chroma.2014.05.059

Chiral amine organocatalysts for the syn-aldol reaction involving substituted benzaldehydes and hydroxyacetone

Dhruba Sarkar, Kurt Harman, Subrata Ghosh and Allan D. Headley

Tetrahedron: Asymmetry, 2011, 22, 1051
DOI: 10.1016/j.tetasy.2011.05.021

Pyrrolidine-based chiral pyridinium ionic liquids (ILs) as recyclable and highly efficient organocatalysts for the asymmetric Michael addition reactions

Bukuo Ni, Qianying Zhang and Allan D. Headley

Tetrahedron Letters, 2008, 49, 1249
DOI: 10.1016/j.tetlet.2007.12.024

Highly enantioselective Michael addition of ketones to nitroolefins catalyzed by (S)-pyrrolidine arenesulfonamide

Bukuo Ni, Qianying Zhang and Allan D. Headley

Tetrahedron: Asymmetry, 2007, 18, 1443
DOI: 10.1016/j.tetasy.2007.05.037

Synthesis of novel chiral imidazolium-based ionic liquids derived from isosorbide and their applications in asymmetric aza Diels–Alder reaction

Olivier Nguyen Van Buu, Audrey Aupoix and Giang Vo-Thanh

Tetrahedron, 2009, 65, 2260
DOI: 10.1016/j.tet.2009.01.055

Novel pyrrolidine-aminobenzimidazole bifunctional organocatalysts for asymmetric nitro-Michael reactions in brine

Jian Lin, Hua Tian, Yi-Jun Jiang, Wen-Bo Huang, Liang-Yu Zheng and Suo-Qin Zhang

Tetrahedron: Asymmetry, 2011, 22, 1434
DOI: 10.1016/j.tetasy.2011.08.002

Synthesis of spiro bis(1,2,3-triazolium) salts as chiral ionic liquids

Yasushi Yoshida, Shinobu Takizawa and Hiroaki Sasai

Tetrahedron Letters, 2011, 52, 6877
DOI: 10.1016/j.tetlet.2011.09.152

Novel chiral ammonium ionic liquids as efficient organocatalysts for asymmetric Michael addition of aldehydes to nitroolefins

Wan-Hui Wang, Xiang-Bo Wang, Koichi Kodama, Takuji Hirose and Guang-You Zhang

Tetrahedron, 2010, 66, 4970
DOI: 10.1016/j.tet.2010.05.030

Pyrrolidine‐Camphor Derivative as an Organocatalyst for Asymmetic Michael Additions of α,α‐Disubstituted Aldehydes to β‐Nitroalkenes: Construction of Quaternary Carbon‐Bearing Aldehydes under Solvent‐Free Conditions

Chihliang Chang, Ssu‐Hsien Li, Raju Jannapu Reddy and Kwunmin Chen

Adv Synth Catal, 2009, 351, 1273
DOI: 10.1002/adsc.200800771

A Highly Enantioselective and Efficient Synthesis of New Pyrimidine‐Fused Spiro[indoline‐3,4′‐pyran]s Promoted by a Novel Chiral Ionic Liquid

Amin Ahmadkhani, Kurosh Rad‐Moghadam and Saeedeh Toorchi Roudsari

ChemistrySelect, 2019, 4, 10442
DOI: 10.1002/slct.201902231

Applications of Chiral Ionic Liquids

Katharina Bica and Peter Gaertner

Eur J Org Chem, 2008, 2008, 3235
DOI: 10.1002/ejoc.200701107

Ionic liquids as substrate-specific recoverable solvents and catalysts of regio-, stereo- and enantioselective organic reactions

Sergei G. Zlotin and Nina N. Makhova

Mendeleev Communications, 2010, 20, 63
DOI: 10.1016/j.mencom.2010.03.001

Chiral Imidazolium Ionic Liquids Derived from (S)‐Prolinamine as Organocatalysts in the Asymmetric Michael Reaction and Michael‐Aldol Cascade Reaction under Solvent‐Free Conditions

Arturo Obregón‐Zúñiga, Marco Guerrero‐Robles and Eusebio Juaristi

Eur J Org Chem, 2017, 2017, 2692
DOI: 10.1002/ejoc.201700133

Enhanced reactivity and enantioselectivity in catalytic glyoxylate-ene reactions using chiral bis(oxazoline)–copper complex in an ionic liquid

Mina Kim, Han Saem Jeong, Chang-Eun Yeom and B. Moon Kim

Tetrahedron: Asymmetry, 2012, 23, 1019
DOI: 10.1016/j.tetasy.2012.06.004

A Recyclable Organocatalyst for Asymmetric Michael Addition

Mei Yang, Yuecheng Zhang, Jiquan Zhao, Qiusheng Yang, Yi Ma and Xiaohui Cao

Catal Lett, 2016, 146, 587
DOI: 10.1007/s10562-016-1693-x

Polystyrene‐Supported Diarylprolinol Ethers as Highly Efficient Organocatalysts for Michael‐Type Reactions

Esther Alza, Sonia Sayalero, Pinar Kasaplar, Diana Almaşi and Miquel A. Pericàs

Chemistry A European J, 2011, 17, 11585
DOI: 10.1002/chem.201101730

Recyclable Stereoselective Catalysts

Alexandre F. Trindade, Pedro M. P. Gois and Carlos A. M. Afonso

Chem. Rev., 2009, 109, 418
DOI: 10.1021/cr800200t

Highly enantioselective Michael addition reactions in water catalyzed by an insoluble MPS-supported 4-sulfonamidyl prolinol tert-butyldiphenylsilyl ether

Yongming Chuan, Guihua Chen and Yungui Peng

Tetrahedron Letters, 2009, 50, 3054
DOI: 10.1016/j.tetlet.2009.04.011

Solvent‐Controlled Friedel–Crafts Reaction for the Synthesis of 3‐Indolyl‐3‐hydroxy Oxindoles and 3, 3‐Diindolyl Oxindoles Catalyzed by Dabco‐Base Ionic Liquids

Jun Tong, Yu‐Wei Li and Da‐Zhen Xu

ChemistrySelect, 2017, 2, 3799
DOI: 10.1002/slct.201700603

Novel Class of Reversible Chiral Ionic Liquids Derived from Natural Amino Acids: Synthesis and Characterization.

Lucie Bouchardy, Violeta Rodriguez‐Ruiz, Chloée Bournaud, François‐Didier Boyer, Martial Toffano, Patrick Judeinstein and Giang Vo‐Thanh

ChemistrySelect, 2018, 3, 958
DOI: 10.1002/slct.201702708

A simple, efficient and green procedure for Michael addition catalyzed by [C4dabco]OH ionic liquid

Sanjoy Keithellakpam and Warjeet S. Laitonjam

Chinese Chemical Letters, 2014, 25, 767
DOI: 10.1016/j.cclet.2014.01.032

Ionic Liquid-Supported (ILS) (S)-Pyrrolidine Sulfonamide, a Recyclable Organocatalyst for the Highly Enantioselective Michael Addition to Nitroolefins

Bukuo Ni, Qianying Zhang, Kritanjali Dhungana and Allan D. Headley

Org. Lett., 2009, 11, 1037
DOI: 10.1021/ol900003e

Highly asymmetric Michael additions of α,α-disubstituted aldehydes to β-nitroalkenes promoted by chiral pyrrolidine–thiourea bifunctional catalysts

Jian-Fei Bai, Xiao-Ying Xu, Qing-Chun Huang, Lin Peng and Li-Xin Wang

Tetrahedron Letters, 2010, 51, 2803
DOI: 10.1016/j.tetlet.2010.03.039

Synthesis of new chiral ionic liquids based on (−)-menthol and (−)-borneol

Ricardo Alexandre F. Matos and Carlos Kleber Z. Andrade

Tetrahedron Letters, 2008, 49, 1652
DOI: 10.1016/j.tetlet.2008.01.011

Design and synthesis of spiro bis(1,2,3-triazolium) salts as chiral ionic liquids

Yasushi Yoshida, Shinobu Takizawa and Hiroaki Sasai

Tetrahedron: Asymmetry, 2012, 23, 843
DOI: 10.1016/j.tetasy.2012.06.007

Asymmetric Michael addition reactions of aldehydes with nitrostyrenes catalyzed by functionalized chiral ionic liquids

Qianying Zhang, Bukuo Ni and Allan D. Headley

Tetrahedron, 2008, 64, 5091
DOI: 10.1016/j.tet.2008.03.073

Functionalized Chiral Ionic Liquids: A New Type of Asymmetric Organocatalysts and Nonclassical Chiral Ligands

Sanzhong Luo, Long Zhang and Jin‐Pei Cheng

Chemistry An Asian Journal, 2009, 4, 1184
DOI: 10.1002/asia.200900080

Synthesis, Characterization and Applications of Dicationic Ionic Liquids in Organic Synthesis

Mohammad Javaherian and Seyyed Jafar Saghanezhad

MROC, 2020, 17, 450
DOI: 10.2174/1570193X16666190508091231

Chiral ionic liquids: A compendium of syntheses and applications (2005–2012)

Tharanga Payagala and Daniel W. Armstrong

Chirality, 2012, 24, 17
DOI: 10.1002/chir.21975

Ionic‐Liquid‐Supported (ILS) Catalysts for Asymmetric Organic Synthesis

Bukuo Ni and Allan D. Headley

Chemistry A European J, 2010, 16, 4426
DOI: 10.1002/chem.200902747

Silica gel supported pyrrolidine-based chiral ionic liquid as recyclable organocatalyst for asymmetric Michael addition to nitrostyrenes

Pinhua Li, Lei Wang, Yicheng Zhang and Guanwu Wang

Tetrahedron, 2008, 64, 7633
DOI: 10.1016/j.tet.2008.05.039

Substrate control by means of the chiral cavity of prolinamide derivatives of cholic acid in the organocatalyzed Michael addition of cyclohexanone to nitroolefins

Gian Luigi Puleo and Anna Iuliano

Tetrahedron: Asymmetry, 2008, 19, 2045
DOI: 10.1016/j.tetasy.2008.08.018

An Eco‐Friendly Asymmetric Organocatalytic Conjugate Addition of Malonates to α,β‐Unsaturated Aldehydes: Application on the Synthesis of Chiral Indoles

Karla Santos Feu, Anna Maria Deobald, Senthil Narayanaperumal, Arlene G. Corrêa and Márcio Weber Paixão

Eur J Org Chem, 2013, 2013, 5917
DOI: 10.1002/ejoc.201300431

Solvent free synthesis of cyclic ureas and urethanes by carbonylation method in the basic dicationic ionic liquid catalysts

Ashif H. Tamboli, Harshad A. Bandal and Hern Kim

Chemical Engineering Journal, 2016, 306, 826
DOI: 10.1016/j.cej.2016.08.013

Synthesis of functionalized chiral ammonium, imidazolium, and pyridinium-based ionic liquids derived from (−)-ephedrine using solvent-free microwave activation. Applications for the asymmetric Michael addition

Thi-Kim-Thu Truong and Giang Vo-Thanh

Tetrahedron, 2010, 66, 5277
DOI: 10.1016/j.tet.2010.03.101

Self-assembled proline-amino thioureas as efficient organocatalysts for the asymmetric Michael addition of aldehydes to nitroolefins

Wan-Hui Wang, Takeshi Abe, Xiang-Bo Wang, Koichi Kodama, Takuji Hirose and Guang-You Zhang

Tetrahedron: Asymmetry, 2010, 21, 2925
DOI: 10.1016/j.tetasy.2010.11.025

Silica Gel Supported Dual Acidic Ionic Liquid as a Recyclable and Efficient Catalyst for Esterification and Acetalization Reactions

Qiang Zhang, Hong Su and Jun Luo

AMR, 2011, 233-235, 1336
DOI: 10.4028/www.scientific.net/AMR.233-235.1336

Symmetriebruch in chiralen ionischen Flüssigkeiten: Nachweis durch vibratorisch‐optische Aktivität

Patric Oulevey, Sandra Luber, Birte Varnholt and Thomas Bürgi

Angewandte Chemie, 2016, 128, 11962
DOI: 10.1002/ange.201605792

Ionic Liquid Assisted C-C Bond Formation

Mandeep Kaur, Opinder Kaur, Rahul Badru, Sandeep Kaushal and Pritpal Singh

COC, 2020, 24, 1853
DOI: 10.2174/1385272824999200801022221

Catalytic Ionic‐Liquid Membranes: The Convergence of Ionic‐Liquid Catalysis and Ionic‐Liquid Membrane Separation Technologies

Pavel Izák, Felix D. Bobbink, Martin Hulla, Martina Klepic, Karel Friess, Štěpán Hovorka and Paul J. Dyson

ChemPlusChem, 2018, 83, 7
DOI: 10.1002/cplu.201700293

Recyclable Organocatalysts in Asymmetric Synthesis

Zeynep Dilşad Susam and Cihangir Tanyeli

Asian J Org Chem, 2021, 10, 1251
DOI: 10.1002/ajoc.202100165

Novel Prolinamide–Camphor‐Containing Organocatalysts for Direct Asymmetric Michael Addition of Unmodified Aldehydes to Nitroalkenes

Raju Jannapu Reddy, Hsuan‐Hao Kuan, Tsai‐Yung Chou and Kwunmin Chen

Chemistry A European J, 2009, 15, 9294
DOI: 10.1002/chem.200901254

Synthesis of novel class of 2-oxazolidinone based chiral ionic liquids

Sagar P. Nehate, Himanshu M. Godbole, Girij P. Singh, Jessy E. Mathew and Gautham G. Shenoy

Synthetic Communications, 2018, 48, 2435
DOI: 10.1080/00397911.2018.1496260

Chiral Ionic Liquids Bearing O‐Silylated α,α‐Diphenyl (S)‐ or (R)‐Prolinol Units: Recoverable Organocatalysts for Asymmetric Michael Addition of Nitroalkanes to α,β‐Enals

Oleg V. Maltsev, Alexandr S. Kucherenko, Irina P. Beletskaya, Vladimir A. Tartakovsky and Sergei G. Zlotin

Eur J Org Chem, 2010, 2010, 2927
DOI: 10.1002/ejoc.201000239

“Nonsolvens”‐Anwendungen von ionischen Flüssigkeiten bei Biotransformationen und in der Organokatalyse

Pablo Domínguez de María

Angewandte Chemie, 2008, 120, 7066
DOI: 10.1002/ange.200703305

Amino alcohol-derived chiral ionic liquids: structural investigations toward chiral recognition

Maria Vasiloiu, Isabella Cervenka, Peter Gaertner, Matthias Weil, Christian Schröder and Katharina Bica

Tetrahedron: Asymmetry, 2015, 26, 1069
DOI: 10.1016/j.tetasy.2015.08.009

Mehrfachkatalyse durch zwei chirale Einheiten: eine weitere Dimension in der asymmetrischen Synthese

Susy Piovesana, Daniele M. Scarpino Schietroma and Marco Bella

Angewandte Chemie, 2011, 123, 6340
DOI: 10.1002/ange.201005955

Functionalized Chiral Ionic Liquid as Recyclable Organocatalyst for Asymmetric Michael Addition to Nitrostyrenes.

Bukuo Ni, Qianying Zhang and Allan D. Headley

ChemInform, 2007, 38
DOI: 10.1002/chin.200747025

Enantioselective conjugate addition of ketones to nitroalkenes catalyzed by pyrrolidine‐sulfamides

Jinjia Wang, Jinhua Lao, Quansheng Du, Shaozhen Nie, Zhipeng Hu and Ming Yan

Chirality, 2012, 24, 232
DOI: 10.1002/chir.21987