يعرض 1 - 20 نتائج من 166 نتيجة بحث عن '"R. Gandolfi"', وقت الاستعلام: 0.48s تنقيح النتائج
  1. 1
    Academic Journal
    Hybrid Metal Catalysts as Valuable Tools in Organic Synthesis: An Overview of the Recent Advances in Asymmetric C–C Bond Formation Reactions

    المؤلفون: I. Rimoldi, G. Coffetti, R. Gandolfi, G. Facchetti

    المساهمون: I. Rimoldi, G. Coffetti, R. Gandolfi, G. Facchetti

    مصطلحات موضوعية: artificial metalloenzyme, enantioselective C─C bond formation, homogeneous catalysi, metallo peptide, organometallic complexe, protein engineering, Settore CHEM-03/A - Chimica generale e inorganica, Settore CHEM-07/C - Chimica e biotecnologia delle fermentazioni

    Relation: info:eu-repo/semantics/altIdentifier/pmid/39519731; info:eu-repo/semantics/altIdentifier/wos/WOS:001351762500001; volume:29; issue:21; firstpage:1; lastpage:27; numberofpages:27; journal:MOLECULES; https://hdl.handle.net/2434/1122064

    الاتاحة: https://hdl.handle.net/2434/1122064
    https://doi.org/10.3390/molecules29215090

    View record in BASE

    أضف إلى المفضلة
  2. 2
    Conference
    Recycling of copper contaminants from wastewater as new hybrid catalysts for the synthesis of valuable pharmaceutical intermediates

    المؤلفون: I. Rimoldi, R. Gandolfi, G. Coffetti, M. Colombo, S. Zecchin, L. Cavalca, G. Facchetti

    المساهمون: I. Rimoldi, R. Gandolfi, G. Coffetti, M. Colombo, S. Zecchin, L. Cavalca, G. Facchetti

    مصطلحات موضوعية: Settore CHIM/03 - Chimica Generale e Inorganica, Settore CHIM/11 - Chimica e Biotecnologia delle Fermentazioni, Settore AGR/16 - Microbiologia Agraria

    Relation: ICCC2022 International Conference on Coordination Chemistry : August 28th - September 2nd; http://hdl.handle.net/2434/937012; https://www.iccc2022.com/

    الاتاحة: http://hdl.handle.net/2434/937012
    https://www.iccc2022.com/

    View record in BASE

    أضف إلى المفضلة
  3. 3
    Conference
    One-pot reactions in catalysis: a valuable tool for the synthesis of enantiopure intermediates for pharmaceutical applications

    المؤلفون: G. Facchetti, G. Coffetti, R. Gandolfi, I. Rimoldi

    المساهمون: G. Facchetti, G. Coffetti, R. Gandolfi, I. Rimoldi

    مصطلحات موضوعية: Settore CHIM/03 - Chimica Generale e Inorganica, Settore CHIM/11 - Chimica e Biotecnologia delle Fermentazioni

    Relation: Chemical Catalyst: 3rd Global Virtual Summit on Catalysis & Chemical Engineering; http://hdl.handle.net/2434/937652; https://catalysisconference.mindauthors.com/

    الاتاحة: http://hdl.handle.net/2434/937652
    https://catalysisconference.mindauthors.com/

    View record in BASE

    أضف إلى المفضلة
  4. 4
    Academic Journal
    Hybrid Catalysts from Copper Biosorbing Bacterial Strains and Their Recycling for Catalytic Application in the Asymmetric Addition Reaction of B2(pin)2 on α,β-Unsaturated Chalcones

    المؤلفون: R. Gandolfi, G. Facchetti, L. Cavalca, S. Mazzini, M. Colombo, G. Coffetti, G. Borgonovo, L. Scaglioni, S. Zecchin, I. Rimoldi

    المساهمون: R. Gandolfi, G. Facchetti, L. Cavalca, S. Mazzini, M. Colombo, G. Coffetti, G. Borgonovo, L. Scaglioni, S. Zecchin, I. Rimoldi

    مصطلحات موضوعية: bacterial EPS, heavy metal recycling, copper recovery, wastewater depollution, Settore CHIM/03 - Chimica Generale e Inorganica, Settore CHIM/11 - Chimica e Biotecnologia delle Fermentazioni, Settore AGR/16 - Microbiologia Agraria, Settore CHIM/06 - Chimica Organica

    Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000786768500001; volume:12; firstpage:1; lastpage:12; numberofpages:12; journal:CATALYSTS; http://hdl.handle.net/2434/922488; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85128394353

    الاتاحة: http://hdl.handle.net/2434/922488
    https://doi.org/10.3390/catal12040433

    View record in BASE

    أضف إلى المفضلة
  5. 5
    Academic Journal
    Ruthenium(II) complexes bearing (NNN) ligand : catalytic evaluation of different solvent-mediated coordination modes

    المؤلفون: S. Pellegrino, G. Facchetti, R. Gandolfi, M. Fuse`, E. Erba, Isabella Rimoldi

    المساهمون: S. Pellegrino, G. Facchetti, R. Gandolfi, M. Fuse`, E. Erba, I.S. Rimoldi

    مصطلحات موضوعية: tridentate ligand, asymmetric hydrogen transfer, asymmetric ketones reduction, Settore CHIM/03 - Chimica Generale e Inorganica, Settore CHIM/06 - Chimica Organica, Settore CHIM/11 - Chimica e Biotecnologia delle Fermentazioni

    Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000419340500006; volume:96; issue:1; firstpage:40; lastpage:43; numberofpages:4; journal:CANADIAN JOURNAL OF CHEMISTRY; http://hdl.handle.net/2434/547877; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85040254626

    الاتاحة: http://hdl.handle.net/2434/547877
    https://doi.org/10.1139/cjc-2017-0487

    View record in BASE

    أضف إلى المفضلة
  6. 6
    Academic Journal
    Synthesis and biological evaluation of new natural phenolic (2E,4E,6E)-Octa-2,4,6-trienoic esters

    المؤلفون: R. Gandolfi, A. Contini, D. Pinto, B. Marzani, S. Pandini, D. Nava, E. R. E. Pini

    المساهمون: R. Gandolfi, A. Contini, D. Pinto, B. Marzani, S. Pandini, D. Nava, E.R.E. Pini

    مصطلحات موضوعية: natural product, selective esterification, biocatalysi, antioxidant activity, anti-inflammatory activity, Settore CHIM/06 - Chimica Organica, Settore CHIM/11 - Chimica e Biotecnologia delle Fermentazioni

    Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000418421800005; volume:14; issue:12; firstpage:1; lastpage:14; numberofpages:14; journal:CHEMISTRY & BIODIVERSITY; http://hdl.handle.net/2434/528505; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85037648956

    الاتاحة: http://hdl.handle.net/2434/528505
    https://doi.org/10.1002/cbdv.201700294

    View record in BASE

    أضف إلى المفضلة
  7. 7
    Conference
    Design of a fully automated system for the synthesis of pharmaceutically relevant building blocks exploiting immobilized Rhodotorula rubra and new solvent systems

    المؤلفون: F. Annunziata, A. Guaglio, P. Conti, R. Gandolfi, L. Tamborini

    المساهمون: F. Annunziata, A. Guaglio, P. Conti, R. Gandolfi, L. Tamborini

    مصطلحات موضوعية: Settore CHIM/08 - Chimica Farmaceutica

    Relation: Paul Ehrlich virtual meeting (PEVM); http://hdl.handle.net/2434/859745

    الاتاحة: http://hdl.handle.net/2434/859745

    View record in BASE

    أضف إلى المفضلة
  8. 8
    Conference
    A fully integrated eco-friendly continuous synthesis of pharmaceutically relevant building blocks exploiting immobilized Rhodotorula rubra

    المؤلفون: F. Annunziata, A. Guaglio, R. Gandolfi, L. Tamborini

    المساهمون: F. Annunziata, A. Guaglio, R. Gandolfi, L. Tamborini

    مصطلحات موضوعية: Settore CHIM/08 - Chimica Farmaceutica

    Relation: BNCM; http://hdl.handle.net/2434/853412

    الاتاحة: http://hdl.handle.net/2434/853412

    View record in BASE

    أضف إلى المفضلة
  9. 9
    Academic Journal
    Ctr-1 Mets7 motif inspiring new peptide ligands for Cu(i)-catalyzed asymmetric Henry reactions under green conditions

    المؤلفون: S. Pellegrino, G. Facchetti, A. Contini, M.L. Gelmi, E. Erba, R. Gandolfi, I. Rimoldi

    المساهمون: S. Pellegrino, G. Facchetti, A. Contini, M.L. Gelmi, E. Erba, R. Gandolfi, I. Rimoldi

    مصطلحات موضوعية: Biotin-streptavidin technology, copper transport protein, Alpha-amino-acid, artificial metalloenzyme, metallopeptide catalyst, secondary structure, CU-II, design, complexe, chemistry, Settore CHIM/06 - Chimica Organica, Settore CHIM/03 - Chimica Generale e Inorganica, Settore CHIM/11 - Chimica e Biotecnologia delle Fermentazioni

    Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000381513100096; volume:6; issue:75; firstpage:71529; lastpage:71533; numberofpages:5; journal:RSC ADVANCES; http://hdl.handle.net/2434/430026; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84979903122

    الاتاحة: http://hdl.handle.net/2434/430026
    https://doi.org/10.1039/c6ra16255j

    View record in BASE

    أضف إلى المفضلة
  10. 10
    Academic Journal
    Efficient methodology to produce a duloxetine precursor using whole cells of Rhodotorula rubra

    المؤلفون: I. Rimoldi, G. Facchetti, D. Nava, M.L. Contente, R. Gandolfi

    المساهمون: I. Rimoldi, G. Facchetti, D. Nava, M.L. Contente, R. Gandolfi

    مصطلحات موضوعية: Fungus curvularia-lunata, asymmetric transfer hydrogenation, beta-hydroxy nitrile, bakers-yeast, chemoenzymatic synthesi, carbonyl reductase, keto nitrile, alkylation, biotransformation, (S)-duloxetine, Settore CHIM/11 - Chimica e Biotecnologia delle Fermentazioni, Settore CHIM/03 - Chimica Generale e Inorganica

    Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000375811800003; volume:27; issue:9-10; firstpage:389; lastpage:396; numberofpages:8; journal:TETRAHEDRON-ASYMMETRY; http://hdl.handle.net/2434/417779; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84963945510

    الاتاحة: http://hdl.handle.net/2434/417779
    https://doi.org/10.1016/j.tetasy.2016.04.002

    View record in BASE

    أضف إلى المفضلة
  11. 11
    Academic Journal
    Evaluation of chemical diversity of biotinylated chiral 1,3-diamines as a catalytic moiety in artificial imine reductase

    المؤلفون: M. Pellizzoni, G. Facchetti, R. Gandolfi, M. Fusè, A. Contini, I. Rimoldi

    المساهمون: M. Pellizzoni, G. Facchetti, R. Gandolfi, M. Fusè, A. Contini, I. Rimoldi

    مصطلحات موضوعية: asymmetric transfer hydrogenation, chiral diamine, imino reductase, metalloenzyme, salsolidine, Settore CHIM/03 - Chimica Generale e Inorganica, Settore CHIM/06 - Chimica Organica, Settore CHIM/11 - Chimica e Biotecnologia delle Fermentazioni

    Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000379528500009; volume:8; issue:9; firstpage:1665; lastpage:1670; numberofpages:6; journal:CHEMCATCHEM; http://hdl.handle.net/2434/417677; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84979492152

    الاتاحة: http://hdl.handle.net/2434/417677
    https://doi.org/10.1002/cctc.201600116

    View record in BASE

    أضف إلى المفضلة
  12. 12
    Academic Journal
    Simple 1,3-diamines and their application as ligands in ruthenium(ii) catalysts for asymmetric transfer hydrogenation of aryl ketones

    المؤلفون: G. Facchetti, R. Gandolfi, M. Fuse, D. Zerla, E. Cesarotti, M. Pellizzoni, I. Rimoldi

    المساهمون: G. Facchetti, R. Gandolfi, M. Fuse, D. Zerla, E. Cesarotti, M. Pellizzoni, I. Rimoldi

    مصطلحات موضوعية: Fungus curvularia-lunata, carbonyl reductase, aromatic ketone, sporobolomyces-salmonicolor, enantioselective reduction, water, alkylation, complexe, diethylzinc, nitriles, Settore CHIM/03 - Chimica Generale e Inorganica, Settore CHIM/11 - Chimica e Biotecnologia delle Fermentazioni

    Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000354199900077; volume:39; issue:5; firstpage:3792; lastpage:3800; numberofpages:9; journal:NEW JOURNAL OF CHEMISTRY; http://hdl.handle.net/2434/274003; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84929119531

    الاتاحة: http://hdl.handle.net/2434/274003
    https://doi.org/10.1039/c5nj00110b

    View record in BASE

    أضف إلى المفضلة
  13. 13
    Conference
    Production of optically pure molecules by asymmetric reductions with yeasts

    المؤلفون: R. Gandolfi, D. Romano, F.E. Molinari, I. Rimoldi

    المساهمون: R. Gandolfi, D. Romano, F.E. Molinari, I. Rimoldi

    مصطلحات موضوعية: Settore CHIM/11 - Chimica e Biotecnologia delle Fermentazioni, Settore CHIM/03 - Chimica Generale e Inorganica

    Relation: National Meeting della Società Italiana di Microbiologia Generale e biotecnologie Microbiche; http://hdl.handle.net/2434/147732

    الاتاحة: http://hdl.handle.net/2434/147732

    View record in BASE

    أضف إلى المفضلة
  14. 14
    Academic Journal
    New insights into glycopeptide antibiotic binding to cell wall precursors using SPR and NMR spectroscopy

    المؤلفون: J. Treviño, C. Bayõn, A. Ardá, F. Marinelli, R. Gandolfi, F. Molinari, J. Jimenez Barbero, M. J. Hernáiz

    المساهمون: J. Treviño, C. Bayõn, A. Ardá, F. Marinelli, R. Gandolfi, F. Molinari, J. Jimenez Barbero, M.J. Hernáiz

    مصطلحات موضوعية: antibiotic, glycopeptide, NMR spectroscopy, surface plasmon resonance, teicoplanin, Settore CHIM/11 - Chimica e Biotecnologia delle Fermentazioni

    Relation: info:eu-repo/semantics/altIdentifier/pmid/24805824; info:eu-repo/semantics/altIdentifier/wos/WOS:000337617500023; volume:20; issue:24; firstpage:7363; lastpage:7372; numberofpages:10; journal:CHEMISTRY-A EUROPEAN JOURNAL; http://hdl.handle.net/2434/248973; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84902116609

    الاتاحة: http://hdl.handle.net/2434/248973
    https://doi.org/10.1002/chem.201303310

    View record in BASE

    أضف إلى المفضلة
  15. 15
    Academic Journal
    Production of fructooligosaccharides by mycelium-bound transfructosylation activity present in Cladosporium cladosporioides and Penicilium sizovae

    المؤلفون: P. Zambelli, L. Fernandez Arrojo, D. Romano, P. Santos Moriano, M. Gimeno Perez, A. Poveda, R. Gandolfi, M. Fernández Lobato, F. Molinari, F. J. Plou

    المساهمون: P. Zambelli, L. Fernandez Arrojo, D. Romano, P. Santos Moriano, M. Gimeno Perez, A. Poveda, R. Gandolfi, M. Fernández Lobato, F. Molinari, F.J. Plou

    مصطلحات موضوعية: Fructooligosaccharide, Transfructosylation, Prebiotic, Bioactive oligosaccharide, Blastose, Settore CHIM/11 - Chimica e Biotecnologia delle Fermentazioni, Settore AGR/16 - Microbiologia Agraria

    Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000347761100020; volume:49; issue:12; firstpage:2174; lastpage:2180; numberofpages:7; journal:PROCESS BIOCHEMISTRY; http://hdl.handle.net/2434/241434; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84914170198

    الاتاحة: http://hdl.handle.net/2434/241434
    https://doi.org/10.1016/j.procbio.2014.09.021

    View record in BASE

    أضف إلى المفضلة
  16. 16
    Academic Journal
    Direct conversion of polyconjugated compounds into their corresponding carboxylic acids by Acetobacter aceti

    المؤلفون: E.R.E. Pini, V. Bertacche, F.E. Molinari, D. Romano, R. Gandolfi

    المساهمون: E.R.E. Pini, V. Bertacche, F.E. Molinari, D. Romano, R. Gandolfi

    مصطلحات موضوعية: Settore CHIM/11 - Chimica e Biotecnologia delle Fermentazioni, Settore CHIM/06 - Chimica Organica

    Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000258841100006; volume:64; issue:37; firstpage:8638; lastpage:8641; journal:TETRAHEDRON; http://hdl.handle.net/2434/44604; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-48049083733

    الاتاحة: http://hdl.handle.net/2434/44604
    https://doi.org/10.1016/j.tet.2008.07.011

    View record in BASE

    أضف إلى المفضلة
  17. 17
    Conference
    Conventional and non-conventional catalytic systems for the asymmetric reduction of cyclic imines

    المؤلفون: G. Facchetti, R. Bucci, S. Pellegrino, M. Fusè, R. Gandolfi, I. Rimoldi

    المساهمون: G. Facchetti, R. Bucci, S. Pellegrino, M. Fusè, R. Gandolfi, I. Rimoldi

    مصطلحات موضوعية: Settore CHIM/03 - Chimica Generale e Inorganica

    Relation: Congresso del Gruppo Interdivisionale di Chimica Organometallica della Società Chimica Italiana; http://hdl.handle.net/2434/583708

    الاتاحة: http://hdl.handle.net/2434/583708

    View record in BASE

    أضف إلى المفضلة
  18. 18
    Book
    Dynamic kinetic resolution of calchones by chemo- and bio-catalytic approach

    المؤلفون: G. Facchetti, F. Meneghetti, R. Gandolfi, I. Rimoldi

    المساهمون: C.S. Marque, E.P. Carreiro, A.J. Burke, G. Facchetti, F. Meneghetti, R. Gandolfi, I. Rimoldi

    مصطلحات موضوعية: Settore CHIM/03 - Chimica Generale e Inorganica

    Relation: info:eu-repo/semantics/altIdentifier/isbn/9789898550415; ispartofbook:ISySyCat : International Symposium on Synthesis and Catalysis : Book of Abstracts; International Symposium on Synthesis and Catalysis; firstpage:247; lastpage:247; numberofpages:1; alleditors:C.S. Marques, E.P. Carreiro, A.J. Burke; http://hdl.handle.net/2434/763109

    الاتاحة: http://hdl.handle.net/2434/763109

    View record in BASE

    أضف إلى المفضلة
  19. 19
    Book
    Vancomycin/D-Ala-D-Ala interaction: a new strategy to obtain artificial imine reductases

    المؤلفون: G. Facchetti, S. Pellegrino, R. Gandolfi, M. Fusè, I. Rimoldi

    المساهمون: C.S. Marque, E.P. Carreiro, A.J. Burke, G. Facchetti, S. Pellegrino, R. Gandolfi, M. Fusè, I. Rimoldi

    مصطلحات موضوعية: Settore CHIM/03 - Chimica Generale e Inorganica

    Relation: info:eu-repo/semantics/altIdentifier/isbn/9789898550415; ispartofbook:ISySyCat : International Symposium on Synthesis and Catalysis : Book of Abstracts; International Symposium on Synthesis and Catalysis; firstpage:246; lastpage:246; numberofpages:1; alleditors:C.S. Marques, E.P. Carreiro, A.J. Burke; http://hdl.handle.net/2434/763124

    الاتاحة: http://hdl.handle.net/2434/763124

    View record in BASE

    أضف إلى المفضلة
  20. 20
    Book
    New Mets7 motif metallopeptide catalysts for Cu(I)-catalyzed asymmetric Henry reaction

    المؤلفون: S. Pellegrino, G. Facchetti, A. Contini, M.L. Gelmi, E. Erba, R. Gandolfi, I. Rimoldi

    المساهمون: S. Pellegrino, G. Facchetti, A. Contini, M.L. Gelmi, E. Erba, R. Gandolfi, I. Rimoldi

    مصطلحات موضوعية: Settore CHIM/03 - Chimica Generale e Inorganica, Settore CHIM/06 - Chimica Organica, Settore BIO/14 - Farmacologia

    Relation: ispartofbook:Cafc11 : Book of Abstracts; International Congress on Catalysis and Fine Chemicals; firstpage:106; lastpage:106; numberofpages:1; http://hdl.handle.net/2434/505357

    الاتاحة: http://hdl.handle.net/2434/505357

    View record in BASE

    أضف إلى المفضلة
أدوات البحث: أحصل على تغذية RSS – أرسل هذا البحث بالبريد الإلكتروني – حفظ البحث – جدول التنبيهات: لا شيء