Miquel A. Pericàs

Affiliations: 
Institute of Chemical Research of Catalonia (ICIQ) 
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"Miquel Pericàs"
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Wang S, Rodríguez-Escrich C, Fianchini M, et al. (2019) Diastereodivergent Enantioselective [8 + 2] Annulation of Tropones and Enals Catalyzed by N-Heterocyclic Carbenes. Organic Letters
Cañellas S, Alonso P, Pericàs MÀ. (2018) Development of C-Symmetric Chiral Bifunctional Triamines: Synthesis and Application in Asymmetric Organocatalysis. Organic Letters
Clot-Almenara L, Rodríguez-Escrich C, Pericàs MA. (2018) Desymmetrisation of meso-diones promoted by a highly recyclable polymer-supported chiral phosphoric acid catalyst Rsc Advances. 8: 6910-6914
Biosca M, Margalef J, Caldentey X, et al. (2018) Computationally Guided Design of a Readily Assembled Phosphite–Thioether Ligand for a Broad Range of Pd-Catalyzed Asymmetric Allylic Substitutions Acs Catalysis. 8: 3587-3601
Pericàs MA, Wang S, Rodríguez-Escrich C. (2017) Catalytic Asymmetric [8+2] Annulation Reactions Promoted by a Recyclable Immobilized Isothiourea. Angewandte Chemie (International Ed. in English)
Wang S, Izquierdo J, Rodríguez-Escrich C, et al. (2017) Asymmetric [4 + 2] Annulation Reactions Catalyzed by a Robust, Immobilized Isothiourea Acs Catalysis. 7: 2780-2785
Cañellas S, Ayats C, Henseler AH, et al. (2017) A Highly Active Polymer-Supported Catalyst for Asymmetric Robinson Annulations in Continuous Flow Acs Catalysis. 7: 1383-1391
Hempel C, Maichle-Mössmer C, Pericàs MA, et al. (2017) Modular Synthesis of Triazole-based Chiral Iodoarenes for Enantioselective Spirocyclizations Advanced Synthesis & Catalysis. 359: 2931-2941
Arenas I, Ferrali A, Rodríguez-Escrich C, et al. (2017) cis-4-Alkoxydialkyl- and cis-4-Alkoxydiarylprolinol Organocatalysts: High Throughput Experimentation (HTE)-Based and Design of Experiments (DoE)-Guided Development of a Highly Enantioselective aza-Michael Addition of Cyclic Imides to α,β-Unsaturated Aldehydes Advanced Synthesis & Catalysis. 359: 2414-2424
Günler ZI, Companyó X, Alfonso I, et al. (2016) Deciphering the roles of multiple additives in organocatalyzed Michael additions. Chemical Communications (Cambridge, England). 52: 6821-4
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