Multi-enzyme cascade synthesis of the most odorous stereoisomers of the commercial odorant Muguesia®

Journal of Molecular Catalysis B: Enzymatic

Volumn 114, Issue , 2015, Pages 37-41

  Brenna, Elisabetta ^a   Crotti, Michele ^a   Gatti, Francesco G ^a   Monti, Daniela ^b   Parmeggiani, Fabio ^a   Pugliese, Andrea ^a   Santangelo, Sara ^a  

^a POLITECNICO DI MILANO   (Italy)

^b CNR   (Italy)

Author keywords

Alcohol dehydrogenase; Cascade reaction; Chiral fragrance; Ene reductase; Stereoselectivity

Indexed keywords

ENZYMES; ISOMERS; KETONES; STEREOSELECTIVITY;

ALCOHOL DEHYDROGENASE; CASCADE REACTIONS; COFACTOR REGENERATION; ENE-REDUCTASE; ENZYME CASCADES; RELATIVE POSITIONS; STEREOCHEMICAL CONTROL; UNSATURATED KETONES;

STEREOCHEMISTRY;

ALCOHOL DEHYDROGENASE; ENE REDUCTASE; FRAGRANCE; KETONE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE DEHYDROGENASE; UNCLASSIFIED DRUG;

ARTICLE; BIOCATALYSIS; CATALYSIS; ENANTIOSELECTIVITY; ENZYME SYNTHESIS; NONHUMAN; ONE POT SYNTHESIS; REACTION TIME; STEREOCHEMISTRY; STEREOISOMERISM;

EID: 84926198614     PISSN: 13811177     EISSN: 18733158     Source Type: Journal    
DOI: 10.1016/j.molcatb.2014.10.006     Document Type: Article

References (20)

1. E. Brenna, C. Fuganti, F.G. Gatti, and S. Serra Chem. Rev. 111 2011 4036 4072
2. P. Kraft, and A. Mannschreck J. Chem. Educ. 87 2010 598 603
3. R. Gatermann, S. Biselli, H. Hühnerfuss, G.G. Rimkus, S. Franke, M. Hecker, R. Kallenborn, L. Karbe, and W.A. König Arch. Environ. Contam. Toxicol. 42 2002 447 453
4. A. Abate, E. Brenna, C. Fuganti, F.G. Gatti, T. Giovenzana, L. Malpezzi, and S. Serra J. Org. Chem. 70 2005 1281 1290
5. M. Bechtold, E. Brenna, C. Femmer, F.G. Gatti, S. Panke, F. Parmeggiani, and A. Sacchetti Org. Process Res. Dev. 16 2012 269 276
6. S.-M. Lu, and C. Bolm Angew. Chem. Int. Ed. 47 2008 8920 8923
7. E. Brenna, S.L. Cosi, E.E. Ferrandi, F.G. Gatti, D. Monti, F. Parmeggiani, and A. Sacchetti Org. Biomol. Chem. 11 2013 2988 2996
8. F.G. Gatti, F. Parmeggiani, and A. Sacchetti E. Brenna, Synthetic methods for biologically active molecules - exploiting the potential of bioreductions 2013 Wiley-VCH Ch. 3, 2014
9. E. Brenna, F.G. Gatti, A. Manfredi, D. Monti, and F. Parmeggiani Eur. J. Org. Chem. 2011 4015 4022
10. E. Brenna, F.G. Gatti, A. Manfredi, D. Monti, and F. Parmeggiani Org. Process Res. Dev. 16 2012 262 268
11. E. Brenna, F.G. Gatti, A. Manfredi, D. Monti, and F. Parmeggiani Adv. Synth. Catal. 354 2012 2859 2864
12. E. Brenna, F.G. Gatti, A. Manfredi, D. Monti, and F. Parmeggiani Catal. Sci. Technol. 3 2013 1136 1146
13. E. Brenna, M. Crotti, F.G. Gatti, A. Manfredi, D. Monti, F. Parmeggiani, A. Pugliese, and D. Zampieri J. Mol. Catal. B: Enzym. 101 2014 67 72
14. E. Brenna, M. Crotti, F.G. Gatti, A. Manfredi, D. Monti, F. Parmeggiani, S. Santangelo, and D. Zampieri ChemCatChem 6 2014 2425 2431
15. E. Brenna, F.G. Gatti, D. Monti, F. Parmeggiani, and A. Sacchetti ChemCatChem 4 2012 653 659
16. E. Ricca, B. Brucher, and J.H. Schrittwieser Adv. Synth. Catal. 353 2011 2239 2262
17. D. Ghislieri, D. Houghton, A.P. Green, S.C. Willies, and N.J. Turner ACS Catal. 3 2013 2869 2872
18. R.C. Simon, N. Richter, E. Busto, and W. Kroutil ACS Catal. 4 2014 129 143
19. A. Díaz-Rodríguez, W. Borzęcka, I. Lavandera, and V. Gotor ACS Catal. 4 2014 386 393
20. T. Classen, M. Korpak, M. Schölzel, and J. Pietruszka ACS Catal. 4 2014 1321 1331