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Biocatalysis and Biotransformation Volume 22, 2004 - Issue 4

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Chemoenzymatic synthesis of enantiopure 1,4-dihydropyridine derivatives

A. Sobolev Laboratory of Organic Chemistry, Wageningen University, Dreijenplein 8, 6703, HB, Wageningen, The Netherlands; Latvian Institute of Organic Synthesis, Aizkraukles 21, Riga, LV-1006, Latvia

M.C.R. Franssen Laboratory of Organic Chemistry, Wageningen University, Dreijenplein 8, 6703, HB, Wageningen, The NetherlandsCorrespondence[email protected]

G. Duburs Latvian Institute of Organic Synthesis, Aizkraukles 21, Riga, LV-1006, Latvia

Ae. De Groot Laboratory of Organic Chemistry, Wageningen University, Dreijenplein 8, 6703, HB, Wageningen, The Netherlands

Pages 231-252 | Received 17 May 2004, Published online: 11 Jul 2009

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https://doi.org/10.1080/10242420400009939

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Mallikarjuna R. Guda, Grigory. V. Zyryanov, Amit Dubey, Venkata Subbaiah Munagapati & Jet-Chau Wen. (2023) Cytotoxic and Infection-Controlled Investigations of Novel Dihydropyridine Hybrids: An Efficient Synthesis and Molecular-Docking Studies. Pharmaceuticals 16:8, pages 1159.
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Min Han, Shi‐qi Zhang, Xin Cui, Qi‐wei Wang, Guang‐xun Li & Zhuo Tang. (2022) Chiral Phosphoric Acid Catalyzed Enantioselective Desymmetrization of 1,4‐Dihydropyridines by C(sp 3 )−H Bromination . Angewandte Chemie International Edition 61:22.
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Martins Rucins, Aiva Plotniece, Eiva Bernotiene, Wei-Bor Tsai & Arkadij Sobolev. (2020) Recent Approaches to Chiral 1,4-Dihydropyridines and their Fused Analogues. Catalysts 10:9, pages 1019.
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Egils Bisenieks, Janis Poikans, Aiva Plotniece, Eiva Bernotiene, Wei-Bor Tsai & Arkadij Sobolev. (2020) Sodium N-(3,5-Bis(ethoxycarbonyl)-2,6-dimethyl-1,4-dihydropyridine-4-carbonyl)-l-methioninate. Molbank 2020:3, pages M1148.
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Eduarda Santa-Helena, Diego da Costa Cabrera, Stefanie Teixeira, Jonathan Rodrigues, Micheli Castro, Marcelo G. Montes D’Oca, Luiz Eduardo Maia Nery & Carla Amorim Neves Gonçalves. (2019) New fatty dihydropyridines present cardioprotective potential in H9c2 cardioblasts submitted to simulated ischemia and reperfusion. Biomedicine & Pharmacotherapy 109, pages 1532-1540.
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Vemulapati Hanuman Reddy, Avula Krishna Kumari, Guda Mallikarjuna Reddy, Yellala Venkata Rami Reddy, Jarem Raul Garcia, Grigory V. Zyryanov, Nemallapudi Bakthavatchala Reddy & Aluru Rammohan. (2019) Environmentally benign one-pot multicomponent synthesis of 1,4-dihydropyridine derivatives applying montmorillonite K10 as reusable catalyst. Chemistry of Heterocyclic Compounds 55:1, pages 60-65.
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Brigita Vigante, Martins Rucins, Aiva Plotniece, Karlis Pajuste, Iveta Luntena, Brigita Cekavicus, Egils Bisenieks, Rufus Smits, Gunars Duburs & Arkadij Sobolev. (2015) Direct Aminolysis of Ethoxycarbonylmethyl 1,4-Dihydropyridine-3-carboxylates. Molecules 20:11, pages 20341-20354.
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Susana Y. Torres, Yamila Verdecia & Francisca Rebolledo. (2015) Chemoenzymatic approach to optically active 1,4-dihydropyridine derivatives. Tetrahedron 71:23, pages 3976-3984.
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Z. Andzans, A. Krauze, I. Adlere, L. Krasnova & G. Duburs. (2013) Synthesis and enantioselective lipase-catalyzed kinetic resolution of methyl 6-(methoxycarbonyl-methyl)sulfanyl-1,4-dihydropyridine-3-carboxylates. Chemistry of Heterocyclic Compounds 49:3, pages 421-427.
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Kuktae Kwon, Jung A. Shin & Hee-Yoon Lee. (2011) A facile synthesis of (S)-felodipine. Tetrahedron 67:52, pages 10222-10228.
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. (2009) Anniversaries and dates. Chemistry of Heterocyclic Compounds 45:5, pages 623-626.
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Francisco Palacios, Esther Herrán, Gloria Rubiales & Concepción Alonso. (2007) Regioselective synthesis of pyridines and dihydropyridines derived from β-amino acids and aminophosphonates by reaction of N-vinylic phosphazenes with α,β-unsaturated ketones. Tetrahedron 63:25, pages 5669-5676.
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Ashok K. Prasad, Chandrani Mukherjee, Sunil K. Singh, Raju Brahma, Rajpal Singh, Rajendra K. Saxena, Carl E. Olsen & Virinder S. Parmar. (2006) Novel selective biocatalytic deacetylation studies on dihydropyrimidinones. Journal of Molecular Catalysis B: Enzymatic 40:3-4, pages 93-100.
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Guan-Wu Wang & Chun-Bao Miao. (2006) Environmentally benign one-pot multi-component approaches to the synthesis of novel unsymmetrical 4-arylacridinediones. Green Chemistry 8:12, pages 1080.
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A. Sobolev, M. C. R. Franssen, G. Duburs & Ae. de Groot. (2005) Chemoenzymatic Synthesis of Enantiopure 1,4‐Dihydropyridine Derivatives. ChemInform 36:24.
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Chemoenzymatic synthesis of enantiopure 1,4-dihydropyridine derivatives

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Chemoenzymatic synthesis of enantiopure 1,4-dihydropyridine derivatives

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