| Year |
Citation |
Score |
| 2010 |
Wang S, Chen G, Kayser MM, Iwaki H, Lau PCK, Hasegawa Y. ChemInform Abstract: Baeyer-Villiger Oxidations Catalyzed by Engineered Microorganisms: Enantioselective Synthesis of δ-Valerolactones with Functionalized Chains. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200246034 |
0.386 |
|
| 2010 |
Mihovilovic MD, Chen G, Wang S, Kyte B, Rochon F, Kayser MM, Stewart JD. ChemInform Abstract: Asymmetric Baeyer-Villiger Oxidations of 4-Mono- and 4,4-Disubstituted Cyclohexanones by Whole Cells of Engineered Escherichia coli. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200127162 |
0.392 |
|
| 2010 |
Kayser M, Chen G, Stewart J. ChemInform Abstract: “Designer Yeast”: An Enantioselective Oxidizing Reagent for Organic Synthesis Cheminform. 30: no-no. DOI: 10.1002/CHIN.199916303 |
0.337 |
|
| 2010 |
KAYSER MM, CHEN G, STEWART JD. ChemInform Abstract: Enantio- and Regioselective Baeyer-Villiger Oxidations of 2- and 3-Substituted Cyclopentanones Using Engineered Bakers′ Yeast. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199911045 |
0.378 |
|
| 2007 |
Clouthier CM, Kayser MM. Biotransformations with engineered E. coli cells expressing wild-type and mutant Baeyer-Villiger monooxygenases under non-growing conditions Journal of Molecular Catalysis B: Enzymatic. 46: 32-36. DOI: 10.1016/j.molcatb.2007.02.001 |
0.324 |
|
| 2006 |
Clouthier CM, Kayser MM, Reetz MT. Designing new Baeyer-Villiger monooxygenases using restricted CASTing. The Journal of Organic Chemistry. 71: 8431-7. PMID 17064016 DOI: 10.1021/Jo0613636 |
0.36 |
|
| 2005 |
Yang Y, Wang F, Rochon FD, Kayser MM. Synthesis of novel optically pure β-lactams Canadian Journal of Chemistry. 83: 28-36. DOI: 10.1139/V04-159 |
0.365 |
|
| 2003 |
Wang S, Kayser MM, Jurkauskas V. Access to optically pure 4- and 5-substituted lactones: a case of chemical-biocatalytical cooperation. The Journal of Organic Chemistry. 68: 6222-8. PMID 12895054 DOI: 10.1021/Jo026605Q |
0.744 |
|
| 2003 |
Kayser MM, Zhao H, Chen G, Feicht A. Asymmetric oxidation of substituted dithianes and dithiolanes by engineered yeast and E.coli expressing cyclohexanone monooxygenase Arkivoc. 2002: 47-62. DOI: 10.3998/Ark.5550190.0003.C06 |
0.516 |
|
| 2003 |
Wang S, Kayser MM, Iwaki H, Lau PC. Monooxygenase-catalyzed Baeyer–Villiger oxidations: CHMO versus CPMO Journal of Molecular Catalysis B: Enzymatic. 22: 211-218. DOI: 10.1016/S1381-1177(03)00036-5 |
0.76 |
|
| 2003 |
Mihovilovic MD, Müller B, Schulze A, Stanetty P, Kayser MM. An enantiodivergent trend in microbial Baeyer-Villiger oxidations of functionalized pentalenones by recombinant whole cells expressing monooxygenases from Acinetobacter and Pseudomonas European Journal of Organic Chemistry. 2243-2249. DOI: 10.1002/Ejoc.200300023 |
0.401 |
|
| 2002 |
Iwaki H, Hasegawa Y, Wang S, Kayser MM, Lau PC. Cloning and characterization of a gene cluster involved in cyclopentanol metabolism in Comamonas sp. strain NCIMB 9872 and biotransformations effected by Escherichia coli-expressed cyclopentanone 1,2-monooxygenase. Applied and Environmental Microbiology. 68: 5671-84. PMID 12406764 DOI: 10.1128/Aem.68.11.5671-5684.2002 |
0.716 |
|
| 2002 |
Kayser MM, Yang Y, Mihovilovic MD, Feicht A, Rochon FD. Baker's yeast-catalyzed synthesis of optically pure 4-tert-butyl-3-hydroxy β-lactam cis-(3R,4S) and trans-(3R,4R) diastereomers Canadian Journal of Chemistry. 80: 796-800. DOI: 10.1139/V02-108 |
0.366 |
|
| 2002 |
Wang S, Chen G, Kayser MM, Iwaki H, Lau PC, Hasegawa Y. Baeyer-Villiger oxidations catalyzed by engineered microorganisms: Enantioselective synthesis of δ-valerolactones with functionalized chains Canadian Journal of Chemistry. 80: 613-621. DOI: 10.1139/V02-035 |
0.748 |
|
| 2002 |
Mihovilovic MD, Müller B, Kayser MM, Stewart JD, Stanetty P. Whole-cell mediated Baeyer-Villiger oxidation of functionalized bicyclo[3.3.0]ketones by recombinant E. coli Synlett. 703-706. DOI: 10.1055/S-2002-25341 |
0.546 |
|
| 2002 |
Mihovilovic MD, Müller B, Kayser MM, Stewart JD, Stanetty P. Whole-cell Mediated Baeyer-Villiger Oxidation of Functionalized Bicyclo[3.3.0]ketones by Recombinant E. coli Synlett. 2002: 0703-0706. DOI: 10.1055/S-2002-25341 |
0.36 |
|
| 2002 |
Mihovilovic MD, Müller B, Kayser MM, Stanetty P. Microbial Baeyer-Villiger Oxidation of Bicyclo[4.3.0]ketones by Two Recombinant E. coli Strains. A Novel Access to Indole Alkaloids Synlett. 2002: 0700-0702. DOI: 10.1055/S-2002-25340 |
0.448 |
|
| 2002 |
Mihovilovic MD, Müller B, Kayser MM, Stanetty P. Microbial Baeyer-Villiger oxidation of bicyclo[4.3.0]ketones by two recombinant E. coli strains. A novel access to indole alkaloids Synlett. 700-702. DOI: 10.1055/S-2002-25340 |
0.555 |
|
| 2001 |
Rodríguez S, Kayser MM, Stewart JD. Highly stereoselective reagents for beta-keto ester reductions by genetic engineering of baker's yeast. Journal of the American Chemical Society. 123: 1547-55. PMID 11456752 DOI: 10.1021/Ja0027968 |
0.425 |
|
| 2001 |
Mihovilovic MD, Chen G, Wang S, Kyte B, Rochon F, Kayser MM, Stewart JD. Asymmetric Baeyer-Villiger oxidations of 4-mono- and 4,4-disubstituted cyclohexanones by whole cells of engineered Escherichia coli. The Journal of Organic Chemistry. 66: 733-8. PMID 11430090 DOI: 10.1021/Jo001292P |
0.755 |
|
| 2001 |
Mihovilovic MD, Müller B, Kayser MM, Stewart JD, Fröhlich J, Stanetty P, Spreitzer H. Baeyer-Villiger oxidations of representative heterocyclic ketones by whole cells of engineered Escherichia coli expressing cyclohexanone monooxygenase Journal of Molecular Catalysis - B Enzymatic. 11: 349-353. DOI: 10.1016/S1381-1177(00)00021-7 |
0.516 |
|
| 2000 |
Rodríguez S, Schroeder KT, Kayser MM, Stewart JD. Asymmetric synthesis of β-hydroxy esters and α-alkyl-β-hydroxy esters by recombinant Escherichia coli expressing enzymes from baker's yeast Journal of Organic Chemistry. 65: 2586-2587. PMID 10789479 DOI: 10.1021/Jo9917036 |
0.357 |
|
| 1999 |
Kayser MM, Mihovilovic MD, Kearns J, Feicht A, Stewart JD. Baker's Yeast-Mediated Reductions of alpha-Keto Esters and an alpha-Keto-beta-Lactam. Two Routes to the Paclitaxel Side Chain. The Journal of Organic Chemistry. 64: 6603-6608. PMID 11674662 DOI: 10.1021/Jo9900681 |
0.376 |
|
| 1999 |
Rodríguez S, Kayser M, Stewart JD. Improving the stereoselectivity of bakers' yeast reductions by genetic engineering Organic Letters. 1: 1153-1155. PMID 10825967 DOI: 10.1021/Ol9901523 |
0.376 |
|
| 1999 |
Kayser M, Chen G, Stewart J. 'Designer yeast': An enantioselective oxidizing reagent for organic synthesis Synlett. 153-158. DOI: 10.1055/S-1999-2553 |
0.433 |
|
| 1999 |
Chen G, Kayser MM, Mihovilovic MD, Mrstik ME, Martinez CA, Stewart JD. Asymmetric oxidations at sulfur catalyzed by engineered strains that overexpress cyclohexanone monooxygenase New Journal of Chemistry. 23: 827-832. DOI: 10.1039/A902283J |
0.559 |
|
| 1999 |
Kayser MM. Designer yeast: A new enantioselective reagent for organic synthesis Journal of Heterocyclic Chemistry. 36: 1533-1537. DOI: 10.1002/Jhet.5570360613 |
0.322 |
|
| 1998 |
Kayser MM, Chen G, Stewart JD. Enantio- and Regioselective Baeyer-Villiger Oxidations of 2- and 3-Substituted Cyclopentanones Using Engineered Bakers' Yeast. The Journal of Organic Chemistry. 63: 7103-7106. PMID 11672341 DOI: 10.1021/Jo980737V |
0.371 |
|
| 1998 |
Stewart JD, Reed KW, Martinez CA, Zhu J, Chen G, Kayser MM. Recombinant baker's yeast as a whole-cell catalyst for asymmetric Baeyer - Villiger oxidations Journal of the American Chemical Society. 120: 3541-3548. DOI: 10.1021/Ja972942I |
0.573 |
|
| 1997 |
Kayser MM, Zhu J, Hooper DL. On the synthesis and the mechanism of formation of halogenated enol lactones Canadian Journal of Chemistry. 75: 1322-1330. DOI: 10.1139/V97-158 |
0.377 |
|
| 1997 |
Kayser MM, Zhu J, Hooper DL. Stabilized haloylides: synthesis and reactivity Canadian Journal of Chemistry. 75: 1315-1321. DOI: 10.1139/V97-157 |
0.312 |
|
| 1996 |
Stewart JD, Reed KW, Zhu J, Chen G, Kayser MM. A "Designer Yeast" That Catalyzes the Kinetic Resolutions of 2-Alkyl-Substituted Cyclohexanones by Enantioselective Baeyer-Villiger Oxidations. The Journal of Organic Chemistry. 61: 7652-7653. PMID 11667712 DOI: 10.1021/Jo961028P |
0.48 |
|
| 1996 |
Stewart JD, Reed KW, Kayser MM. ‘Designer yeast’: a new reagent for enantioselective Baeyer–Villiger oxidations Journal of the Chemical Society-Perkin Transactions 1. 755-757. DOI: 10.1039/P19960000755 |
0.494 |
|
| 1996 |
Stewart JD, Reed KW, Kayser MM. 'Designer yeast': A new reagent for enantioselective Baeyer-Villiger oxidations Journal of the Chemical Society - Perkin Transactions 1. 755-757. |
0.323 |
|
| 1994 |
Hooper DL, Garagan S, Kayser MM. Lithium Cation-Catalyzed Wittig Reactions The Journal of Organic Chemistry. 59: 1126-1128. DOI: 10.1021/Jo00084A034 |
0.333 |
|
| 1993 |
Kayser MM, Hatt KL, Yu H, Hooper DL. On the mechanism of Wittig reactions with cyclic anhydrides. II. Canadian Journal of Chemistry. 71: 1010-1021. DOI: 10.1139/V93-135 |
0.32 |
|
| 1992 |
Kayser MM, Hatt KL, Hooper DL. Mechanism of Wittig reaction with cyclic anhydrides Canadian Journal of Chemistry. 70: 1985-1996. DOI: 10.1139/V92-249 |
0.334 |
|
| 1989 |
Kayser MM, Breau L. On the regioselectivity of Wittig reactions with unsymmetrically substituted succinic anhydrides Canadian Journal of Chemistry. 67: 1401-1410. DOI: 10.1139/V89-215 |
0.338 |
|
| 1989 |
Breau L, Kayser MM. On the regioselectivity of the condensation of stabilized phosphoylids with 3-substituted phthalic anhydrides Canadian Journal of Chemistry. 67: 569-573. DOI: 10.1139/V89-086 |
0.327 |
|
| 1983 |
Kayser MM, Salvador J, Morand P. Changing regioselectivity patterns in metal hydride reductions of unsymmetrically substituted cyclic anhydrides Canadian Journal of Chemistry. 61: 439-441. DOI: 10.1139/V83-078 |
0.315 |
|
| 1982 |
Kayser MM, Salvador J, Morand P, Krishnamurty HG. Metal hydride reductions of unsymmetrically substituted cyclic anhydrides attached to strained ring systems Canadian Journal of Chemistry. 60: 1199-1206. DOI: 10.1139/V82-178 |
0.399 |
|
| 1982 |
Morand P, Salvator J, Kayser MM. Reversal of regioselectivity in the reduction of gem-disubstituted cyclic carboxylic acid anhydrides Journal of the Chemical Society, Chemical Communications. 458-459. DOI: 10.1002/Chin.198238122 |
0.322 |
|
| 1980 |
Kayser MM, Morand P. Regioselectivity of metal hydride reductions of unsymmetrically substituted cyclic anhydrides. systems where "steric hindrance along the preferred reaction path" rationalization is not applicable Canadian Journal of Chemistry. 58: 2484-2490. DOI: 10.1002/Chin.198114129 |
0.347 |
|
| 1973 |
Elliott AJ, Gibson MS, Kayser MM, Pawelchak GA. Smiles Rearrangement in Hydrazonyl Systems: Extension of a Recent 4H-1,3,4-Benzoxadiazine Synthesis Canadian Journal of Chemistry. 51: 4115-4121. DOI: 10.1002/Chin.197414189 |
0.316 |
|
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