Found: 9
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Designer yeast: A new enantioselective reagent for organic synthesis.
- Published in:
- Journal of Heterocyclic Chemistry, 1999, v. 36, n. 6, p. 1533, doi. 10.1002/jhet.5570360613
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- Article
CD-sensitive Zn-porphyrin tweezer host-guest complexes, part 2: Cis- and trans-3-hydroxy-4-aryl/alkyl-β-lactams. A case study.
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- Chirality, 2010, v. 22, n. 1, p. 140, doi. 10.1002/chir.20718
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- Article
An Enantiodivergent Trend in Microbial Baeyer-Villiger Oxidations of Functionalized Pentalenones by Recombinant Whole Cells Expressing Monooxygenases from Acinetobacter and Pseudomonas.
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- European Journal of Organic Chemistry, 2003, v. 2003, n. 12, p. 2243, doi. 10.1002/ejoc.200300023
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- Article
Synthesis of novel optically pure β-lactams.
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- Canadian Journal of Chemistry, 2005, v. 83, n. 1, p. 28, doi. 10.1139/V04-159
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- Article
Baker’s yeast-catalyzed synthesis of optically pure 4-tert-butyl-3-hydroxy beta-lactam cis-(3R,4S) and trans-(3R,4R) diastereomers.
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- Canadian Journal of Chemistry, 2002, v. 80, n. 7, p. 796, doi. 10.1139/v02-108
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- Article
Baeyer-Villiger oxidations catalyzed by engineered microorganisms: Enantioselective synthesis of <font face="symbol">d</font>-valerolactones with functionalized chains.
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- Canadian Journal of Chemistry, 2002, v. 80, n. 6, p. 613, doi. 10.1139/v02-035
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- Article
Directed Evolution as a Method To Create Enantioselective Cyclohexanone Monooxygenases for Catalysis in Baeyer–Villiger ReactionsWe thank the Fonds der Chemischen Industrie for generous support.
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- Angewandte Chemie, 2004, v. 116, n. 31, p. 4167, doi. 10.1002/ange.200460272
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- Article
Directed Evolution as a Method To Create Enantioselective Cyclohexanone Monooxygenases for Catalysis in Baeyer–Villiger ReactionsWe thank the Fonds der Chemischen Industrie for generous support.
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- Angewandte Chemie International Edition, 2004, v. 43, n. 31, p. 4075, doi. 10.1002/anie.200460272
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- Article
Assignment of absolute configuration of 3-hydroxy β-lactams by the NMR 'mix and shake' method.
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- Chirality, 2005, v. 17, n. 3, p. 131, doi. 10.1002/chir.20125
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- Article