@article{SchmidtHauke2014,
  author    = {Schmidt, Bernd and Hauke, Sylvia},
  title     = {Olefin cross metathesis based de novo synthesis of a partially protected L-amicetose and a fully protected L-cinerulose derivative},
  series = {Beilstein journal of organic chemistry},
  volume    = {10},
  journal   = {Beilstein journal of organic chemistry},
  publisher = {Beilstein-Institut zur F{\"o}rderung der Chemischen Wissenschaften},
  address   = {Frankfurt, Main},
  issn      = {1860-5397},
  doi       = {10.3762/bjoc.10.102},
  pages     = {1023 -- 1031},
  year      = {2014},
  abstract  = {Cross metathesis of a lactate derived allylic alcohol and acrolein is the entry point to a de novo synthesis of 4-benzoate protected L-amicetose and a cinerulose derivative protected at C5 and C1.},
  language  = {en}
}
@article{SchmidtHauke2014,
  author    = {Schmidt, Bernd and Hauke, Sylvia},
  title     = {Metathesis-Based de novo synthesis of noviose},
  series = {European journal of organic chemistry},
  volume    = {2014},
  journal   = {European journal of organic chemistry},
  number    = {9},
  publisher = {Wiley-VCH},
  address   = {Weinheim},
  issn      = {1434-193X},
  doi       = {10.1002/ejoc.201301615},
  pages     = {1951 -- 1960},
  year      = {2014},
  abstract  = {The rare carbohydrate L-(+)-noviose was synthesized from enantiomerically pure L-lactate. The configuration at C-4 was established by diastereoselective nucleophilic addition to an in-situ-generated lactaldehyde. The resulting homoallylic alcohol was further transformed into a set of ring-closing metathesis (RCM) precursors. These compounds were converted into noviose in few steps using RCM and RCM-allylic-oxidation sequences.},
  language  = {en}
}
@article{SchmidtHaukeMuehlenberg2014,
  author    = {Schmidt, Bernd and Hauke, Sylvia and Muehlenberg, Nino},
  title     = {Imino glycals via Ruthenium-catalyzed RCM and isomerization},
  series = {Synthesis},
  volume    = {46},
  journal   = {Synthesis},
  number    = {12},
  publisher = {Thieme},
  address   = {Stuttgart},
  issn      = {0039-7881},
  doi       = {10.1055/s-0033-1338615},
  pages     = {1648 -- 1658},
  year      = {2014},
  abstract  = {N-Allyl-N-homoallylamines were converted in one step into cyclic enamides via a ruthenium-catalyzed assisted tandem catalytic ring-closing metathesis-isomerization sequence. The sequence relies on the in situ transformation of a metathesis active Ru-carbene into an isomerization active Ru-hydride by addition of hydroxide as a chemical trigger.},
  language  = {en}
}
@phdthesis{Hauke2013,
  author    = {Hauke, Sylvia},
  title     = {De novo Synthese von L-6-Desoxyzuckern via Ruthenium-Katalysierter Olefinmetathese},
  address   = {Potsdam},
  pages     = {168 S.},
  year      = {2013},
  language  = {de}
}
@article{SchmidtHauke2014,
  author    = {Schmidt, Bernd and Hauke, Sylvia},
  title     = {Cross metathesis of allyl alcohols: how to suppress and how to promote double bond isomerization},
  issn      = {1477-0520},
  doi       = {10.1039/c3ob40167g},
  year      = {2014},
  abstract  = {Under standard conditions the cross metathesis of allyl alcohols and methyl acrylate is accompanied by the formation of ketones, resulting from uncontrolled and undesired double bond isomerization. By conducting the CM in the presence of phenol, the catalyst loading and the reaction time required for quantiative conversion can be reduced, and isomerization can be suppressed. On the other hand, consecutive isomerization can be deliberately promoted by evaporating excess methyl acrylate after completing cross metathesis and by adding a base or silane as chemical triggers.},
  language  = {en}
}
@article{SchmidtHauke2013,
  author    = {Schmidt, Bernd and Hauke, Sylvia},
  title     = {Cross metathesis of allyl alcohols how to suppress and how to promote double bond isomerization},
  series = {Organic \& biomolecular chemistry : an international journal of synthetic, physical and biomolecular organic chemistry},
  volume    = {11},
  journal   = {Organic \& biomolecular chemistry : an international journal of synthetic, physical and biomolecular organic chemistry},
  number    = {25},
  publisher = {Royal Society of Chemistry},
  address   = {Cambridge},
  issn      = {1477-0520},
  doi       = {10.1039/c3ob40167g},
  pages     = {4194 -- 4206},
  year      = {2013},
  abstract  = {Under standard conditions the cross metathesis of allyl alcohols and methyl acrylate is accompanied by the formation of ketones, resulting from uncontrolled and undesired double bond isomerization. By conducting the CM in the presence of phenol, the catalyst loading and the reaction time required for quantiative conversion can be reduced, and isomerization can be suppressed. On the other hand, consecutive isomerization can be deliberately promoted by evaporating excess methyl acrylate after completing cross metathesis and by adding a base or silane as chemical triggers.},
  language  = {en}
}
@misc{SchmidtHauke2013,
  author    = {Schmidt, Bernd and Hauke, Sylvia},
  title     = {Cross metathesis of allyl alcohols},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-95037},
  pages     = {4194 -- 4206},
  year      = {2013},
  abstract  = {Under standard conditions the cross metathesis of allyl alcohols and methyl acrylate is accompanied by the formation of ketones, resulting from uncontrolled and undesired double bond isomerization. By conducting the CM in the presence of phenol, the catalyst loading and the reaction time required for quantiative conversion can be reduced, and isomerization can be suppressed. On the other hand, consecutive isomerization can be deliberately promoted by evaporating excess methyl acrylate after completing cross metathesis and by adding a base or silane as chemical triggers.},
  language  = {en}
}
@article{KafkaHaukeSalcinovicetal.2011,
  author    = {Kafka, Stanislav and Hauke, Sylvia and Salcinovic, Arjana and Soidinsalo, Otto and Urankar, Damijana and Kosmrlj, Janez},
  title     = {Copper(I)-Catalyzed [3+2] Cycloaddition of 3-Azidoquinoline-2,4(1H,3H)-diones with terminal alkynes},
  series = {Molecules},
  volume    = {16},
  journal   = {Molecules},
  number    = {5},
  publisher = {MDPI},
  address   = {Basel},
  issn      = {1420-3049},
  doi       = {10.3390/molecules16054070},
  pages     = {4070 -- 4081},
  year      = {2011},
  abstract  = {3-Azidoquinoline-2,4(1H,3H)-diones 1, which are readily available from 4-hydroxyquinolin-2(1H)-ones 4 via 3-chloroquinoline-2,4(1H, 3H)-diones 5, afford, in copper(I)-catalyzed [3 + 2] cycloaddition reaction with terminal acetylenes, 1,4-disubstituted 1,2,3-triazoles 3 in moderate to excellent yields. The structures of compounds 3 were confirmed by (1)H and (13)C-NMR spectroscopy, combustion analyses and mass spectrometry.},
  language  = {en}
}
@article{SchmidtKrehlHauke2013,
  author    = {Schmidt, Bernd and Krehl, Stefan and Hauke, Sylvia},
  title     = {Assisted tandem catalytic cross metathesis-oxidation in one flask from styrenes to 1,2-Diketones and further to quinoxalines},
  series = {The journal of organic chemistry},
  volume    = {78},
  journal   = {The journal of organic chemistry},
  number    = {11},
  publisher = {American Chemical Society},
  address   = {Washington},
  issn      = {0022-3263},
  doi       = {10.1021/jo4005684},
  pages     = {5427 -- 5435},
  year      = {2013},
  abstract  = {1,2-Diketones were synthesized from styrenes by combining a cross metathesis and a Ru-catalyzed alkene oxidation to an assisted tandem catalytic sequence. The synthesis relies on the use of just one metathesis precatalyst, which was in situ converted to the oxidation catalyst by addition of an alkyl hydroperoxide as a chemical trigger and oxidant. The one-flask sequence can be extended beyond 1,2-diketones to quinoxalines, by condensation of the oxidation products with ortho-phenylenediamine.},
  language  = {en}
}