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| Hauptseite > Publikationsdatenbank > Stereoselective Synthesis of 1,3-diols > print |
| 001 | 52117 | ||
| 005 | 20180211182323.0 | ||
| 024 | 7 | _ | |2 DOI |a 10.1055/s-2006-926315 |
| 024 | 7 | _ | |2 WOS |a WOS:000235670600001 |
| 037 | _ | _ | |a PreJuSER-52117 |
| 041 | _ | _ | |a eng |
| 082 | _ | _ | |a 540 |
| 084 | _ | _ | |2 WoS |a Chemistry, Organic |
| 100 | 1 | _ | |a Bode, S. |b 0 |u FZJ |0 P:(DE-Juel1)VDB12652 |
| 245 | _ | _ | |a Stereoselective Synthesis of 1,3-diols |
| 260 | _ | _ | |a Stuttgart [u.a.] |b Thieme |c 2006 |
| 300 | _ | _ | |a 557 - 588 |
| 336 | 7 | _ | |a Journal Article |0 PUB:(DE-HGF)16 |2 PUB:(DE-HGF) |
| 336 | 7 | _ | |a Output Types/Journal article |2 DataCite |
| 336 | 7 | _ | |a Journal Article |0 0 |2 EndNote |
| 336 | 7 | _ | |a ARTICLE |2 BibTeX |
| 336 | 7 | _ | |a JOURNAL_ARTICLE |2 ORCID |
| 336 | 7 | _ | |a article |2 DRIVER |
| 440 | _ | 0 | |a Synthesis: Journal of Synthetic Organic Chemistry |x 0039-7881 |0 5695 |y 4 |v |
| 500 | _ | _ | |a Record converted from VDB: 12.11.2012 |
| 520 | _ | _ | |a Many polyketide-derived natural products contain a synor anti-1,3-diol unit. No general and simple approach exists for the flexible synthesis of polyols and other polyketide-derived structural units, therefore a multitude of methods for the stereoselective synthesis of 1,3-diols has been developed. Asymmetric homogeneous and heterogeneous hydrogenation and diastereoselective reduction, chain elongation, enzymatic and nonenzymatic desymmetrization, or dynamic kinetic resolution are some of these methods. The development of different methods to synthesize these 1,3-diols stereoselectively is important, as often small structural changes in a molecule result in low yields or low stereoselectivity with a known method. This review article highlights some of the recent developments in this field. |
| 536 | _ | _ | |a Biotechnologie |c PBT |2 G:(DE-HGF) |0 G:(DE-Juel1)FUEK410 |x 0 |
| 588 | _ | _ | |a Dataset connected to Web of Science |
| 650 | _ | 7 | |a J |2 WoSType |
| 653 | 2 | 0 | |2 Author |a asymmetric synthesis |
| 653 | 2 | 0 | |2 Author |a reductions |
| 653 | 2 | 0 | |2 Author |a aldol reactions |
| 653 | 2 | 0 | |2 Author |a biocatalysis |
| 653 | 2 | 0 | |2 Author |a desymmetrizations |
| 653 | 2 | 0 | |2 Author |a alcohols |
| 700 | 1 | _ | |a Wolberg, M. |b 1 |u FZJ |0 P:(DE-Juel1)VDB1800 |
| 700 | 1 | _ | |a Müller, M. |b 2 |u FZJ |0 P:(DE-Juel1)VDB1106 |
| 773 | _ | _ | |a 10.1055/s-2006-926315 |g p. 557 - 588 |p 557 - 588 |q 557 - 588 |0 PERI:(DE-600)2033062-5 |t Synthesis |y 2006 |x 0039-7881 |
| 856 | 7 | _ | |u http://dx.doi.org/10.1055/s-2006-926315 |
| 909 | C | O | |o oai:juser.fz-juelich.de:52117 |p VDB |
| 913 | 1 | _ | |k PBT |v Biotechnologie |l ohne FE |b außerhalb PoF |0 G:(DE-Juel1)FUEK410 |x 0 |
| 914 | 1 | _ | |y 2006 |
| 915 | _ | _ | |0 StatID:(DE-HGF)0010 |a JCR/ISI refereed |
| 920 | 1 | _ | |k IBT-2 |l Biotechnologie 2 |g IBT |z ab 31.10.10 weitergeführt IBG-1 |0 I:(DE-Juel1)VDB56 |x 0 |
| 970 | _ | _ | |a VDB:(DE-Juel1)81854 |
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| 980 | _ | _ | |a I:(DE-Juel1)IBG-1-20101118 |
| 980 | _ | _ | |a UNRESTRICTED |
| 981 | _ | _ | |a I:(DE-Juel1)IBG-1-20101118 |
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