-
1
-
-
0032818397
-
100 Years of Baeyer-Villiger oxidations
-
Renz, M. & Meunier, B. 100 Years of Baeyer-Villiger oxidations. European J. Org. Chem. 4, 737-750 (1999).
-
(1999)
European J .Org. Chem.
, vol.4
, pp. 737-750
-
-
Renz, M.1
Meunier, B.2
-
2
-
-
4644319315
-
The baeyer-villiger reaction: New developments toward greener procedures
-
ten Brink, G. J., Arends, I. W. C. E. & Sheldon, R. A. The Baeyer-Villiger reaction: New developments toward greener procedures. Chem. Rev. 104, 4105-4123 (2004).
-
(2004)
Chem. Rev.
, vol.104
, pp. 4105-4123
-
-
Ten Brink, G.J.1
Arends, I.W.C.E.2
Sheldon, R.A.3
-
3
-
-
84923106400
-
An enzyme cascade synthesis of -caprolactone and its oligomers
-
Schmidt, S. et al. An enzyme cascade synthesis of -caprolactone and its oligomers. Angew. Chem. Int. Ed. 54, 2784-2787 (2015).
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 2784-2787
-
-
Schmidt, S.1
-
4
-
-
77957588918
-
The return of a forgotten polymer : Polycaprolactone in the 21st century
-
Woodruff, Maria A. & Hutmacher, D. W. The return of a forgotten polymer : Polycaprolactone in the 21st century. Prog. Polym. Sci. 35, 1217-1256 (2010).
-
(2010)
Prog. Polym. Sci.
, vol.35
, pp. 1217-1256
-
-
Woodruff Maria, A.1
Hutmacher, D.W.2
-
5
-
-
0030942784
-
Theoretical investigations of the mechanism of the bayer-villiger reaction in nonpolar solvents
-
Okuno, Y. Theoretical Investigations of the Mechanism of the Bayer-Villiger Reaction in Nonpolar Solvents. Chem. Eur. J. 3, 212-218 (1997).
-
(1997)
Chem. Eur. J.
, vol.3
, pp. 212-218
-
-
Okuno, Y.1
-
6
-
-
0034699809
-
A concise synthesis of 3-hydroxyindole-2-carboxylates by a modified baeyer-villiger oxidation
-
Hickman, Z. L., Sturino, C. F. & Lachance, N. A concise synthesis of 3-hydroxyindole-2-carboxylates by a modified Baeyer-Villiger oxidation. Tetrahedron Lett. 41, 8217-8220 (2000).
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 8217-8220
-
-
Hickman, Z.L.1
Sturino, C.F.2
Lachance, N.3
-
7
-
-
38549125462
-
The baeyer-villiger reaction on heterogeneous catalysts
-
Jiménez-Sanchidrián, C. & Ruiz, J. R. The Baeyer-Villiger reaction on heterogeneous catalysts. Tetrahedron 64, 2011-2026 (2008).
-
(2008)
Tetrahedron
, vol.64
, pp. 2011-2026
-
-
Jiménez-Sanchidrián, C.1
Ruiz, J.R.2
-
8
-
-
0031838334
-
Cyclohexanone monooxygenase: A Useful Reagent for Asymmetric Baeyer-Villiger Reactions
-
Stewart, J. D. Cyclohexanone Monooxygenase: A Useful Reagent for Asymmetric Baeyer-Villiger Reactions. Curr. Org. Chem. 2, 195-216 (1998).
-
(1998)
Curr. Org. Chem.
, vol.2
, pp. 195-216
-
-
Stewart, J.D.1
-
9
-
-
80052947538
-
Baeyer-villiger monooxygenases in aroma compound synthesis
-
Fink, M. J., Rudroff, F. & Mihovilovic, M. D. Baeyer-Villiger monooxygenases in aroma compound synthesis. Bioorganic Med. Chem. Lett. 21, 6135-6138 (2011).
-
(2011)
Bioorganic Med. Chem. Lett.
, vol.21
, pp. 6135-6138
-
-
Fink, M.J.1
Rudroff, F.2
Mihovilovic, M.D.3
-
10
-
-
84877301715
-
Cascade biotransformations via enantioselective reduction, oxidation, and hydrolysis: Preparation of (R)-lactones from 2-alkylidenecyclopentanones
-
Liu, J. & Li, Z. Cascade biotransformations via enantioselective reduction, oxidation, and hydrolysis: Preparation of (R)-lactones from 2-alkylidenecyclopentanones. ACS Catal. 3, 908-911 (2013).
-
(2013)
ACS Catal
, vol.3
, pp. 908-911
-
-
Liu, J.1
Li, Z.2
-
12
-
-
84939149187
-
A bi-enzymatic convergent cascade for -caprolactone synthesis employing 1,6-hexanediol as a 'double-smart cosubstrate
-
Kara, S., Bornadel, A., Hatti-Kaul, R. & Hollmann, F. A bi-enzymatic convergent cascade for -caprolactone synthesis employing 1,6-hexanediol as a 'double-smart cosubstrate'. ChemCatChem 7, 2442-2445 (2015).
-
(2015)
ChemCatChem
, vol.7
, pp. 2442-2445
-
-
Kara, S.1
Bornadel, A.2
Hatti-Kaul, R.3
Hollmann, F.4
-
13
-
-
84929956451
-
Directed evolution of phenylacetone monooxygenase as an active catalyst for the baeyervilliger conversion of cyclohexanone to caprolactone
-
Parra, L. P., Acevedo, J. P. & Reetz, M. T. Directed evolution of phenylacetone monooxygenase as an active catalyst for the baeyervilliger conversion of cyclohexanone to caprolactone. Biotechnol. Bioeng. 112, 1354-1364 (2015).
-
(2015)
Biotechnol. Bioeng.
, vol.112
, pp. 1354-1364
-
-
Parra, L.P.1
Acevedo, J.P.2
Reetz, M.T.3
-
14
-
-
84863953159
-
Discovery, application and protein engineering of baeyer-villiger monooxygenases for organic synthesis
-
Balke, K., Kadow, M., Mallin, H., Saß, S. & Bornscheuer, U. T. Discovery, application and protein engineering of Baeyer-Villiger monooxygenases for organic synthesis. Org. Biomol. Chem. 10, 6249-6265 (2012).
-
(2012)
Org. Biomol. Chem.
, vol.10
, pp. 6249-6265
-
-
Balke, K.1
Kadow, M.2
Mallin, H.3
Saß, S.4
Bornscheuer, U.T.5
-
15
-
-
84872977574
-
Baeyer-villiger oxidation with peracid generated in situ by calb-clea catalyzed perhydrolysis
-
Chávez, G., Hatti-Kaul, R., Sheldon, R. A. & Mamo, G. Baeyer-Villiger oxidation with peracid generated in situ by CaLB-CLEA catalyzed perhydrolysis. J. Mol. Catal. B Enzym. 89, 67-72 (2013).
-
(2013)
J. Mol. Catal. B Enzym.
, vol.89
, pp. 67-72
-
-
Chávez, G.1
Hatti-Kaul, R.2
Sheldon, R.A.3
Mamo, G.4
-
16
-
-
34250807300
-
Baeyer-villiger oxidation of substituted cyclohexanones via lipase-mediated perhydrolysis utilizing urea-hydrogen peroxide in ethyl acetate
-
Ríos, M. Y., Salazar, E. & Olivo, H. F. Baeyer-Villiger oxidation of substituted cyclohexanones via lipase-mediated perhydrolysis utilizing urea-hydrogen peroxide in ethyl acetate. Green Chem. 9, 459-462 (2007).
-
(2007)
Green Chem.
, vol.9
, pp. 459-462
-
-
Ríos, M.Y.1
Salazar, E.2
Olivo, H.F.3
-
17
-
-
84985029899
-
Lipase-driven epoxidation is a two-stage synergistic process
-
Tang, Q. et al. Lipase-Driven Epoxidation Is A Two-Stage Synergistic Process. ChemistrySelect 1, 836-839 (2016).
-
(2016)
ChemistrySelect
, vol.1
, pp. 836-839
-
-
Tang, Q.1
-
18
-
-
0037471649
-
Carbon-carbon bonds by hydrolytic enzymes
-
Branneby, C., Carlqvist, P., Magnusson, A., Hult, K. & Brinck, T. Carbon-Carbon Bonds by Hydrolytic Enzymes. J. Am. Chem. Soc. 125, 874-875 (2003).
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 874-875
-
-
Branneby, C.1
Carlqvist, P.2
Magnusson, A.3
Hult, K.4
Brinck, T.5
-
19
-
-
29844436474
-
Fast carbon-carbon bond formation by a promiscuous lipase
-
Svedendahl, M., Hult, K. & Berglund, P. Fast Carbon-Carbon Bond Formation by a Promiscuous Lipase. J. Am. Chem. Soc. 127, 17988-17989 (2005).
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 17988-17989
-
-
Svedendahl, M.1
Hult, K.2
Berglund, P.3
-
20
-
-
54349127157
-
Direct epoxidation in Candida antarctica lipase B studied by experiment and theory
-
Svedendahl, M. et al. Direct epoxidation in Candida antarctica lipase B studied by experiment and theory. ChemBioChem 9, 2443-2451 (2008).
-
(2008)
ChemBioChem
, vol.9
, pp. 2443-2451
-
-
Svedendahl, M.1
-
21
-
-
84963604798
-
Effect of deep eutectic solvent mixtures on lipase activity and stability
-
Kim, S. H. et al. Effect of deep eutectic solvent mixtures on lipase activity and stability. J. Mol. Catal. B Enzym. 128, 65-72 (2016).
-
(2016)
J. Mol. Catal. B Enzym.
, vol.128
, pp. 65-72
-
-
Kim, S.H.1
-
22
-
-
84961753812
-
Enzymatic selective synthesis of 1,3-dag based on deep eutectic solvent acting as substrate and solvent
-
Zeng, C. X., Qi, S. J., Xin, R. P., Yang, B. & Wang, Y. H. Enzymatic selective synthesis of 1,3-DAG based on deep eutectic solvent acting as substrate and solvent. Bioprocess Biosyst. Eng. 38, 2053-2061 (2015).
-
(2015)
Bioprocess Biosyst. Eng.
, vol.38
, pp. 2053-2061
-
-
Zeng, C.X.1
Qi, S.J.2
Xin, R.P.3
Yang, B.4
Wang, Y.H.5
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