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Angewandte Chemie (International ed.), ISSN 1433-7851, 04/2003, Volume 42, Issue 17, pp. 1900 - 1923
Among the many types of transition‐metal‐catalyzed CC bond‐forming reactions, olefin metathesis has come to the fore in recent years owing to the wide range... 
cross‐metathesis | homogeneous catalysis | ring‐opening metathesis | olefins | synthetic methods | Cross-metathesis | Ring-opening metathesis | Synthetic methods | Homogeneous catalysis | Olefins | Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology
Journal Article
Journal of polymer science. Part A, Polymer chemistry, ISSN 0887-624X, 04/2018, Volume 56, Issue 7, pp. 741 - 748
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 02/2014, Volume 53, Issue 7, pp. 1968 - 1972
A broadly applicable Ru‐catalyzed protocol for Z‐selective ring‐opening/cross‐metathesis (ROCM) is disclosed. In addition to reactions relating to terminal... 
olefin metathesis | ring‐opening/cross‐metathesis | ruthenium | alkenes | synthetic methods | ring-opening/cross-metathesis | Surface active agents | Alkenes | Olefins | Ligands | Transformations | Terminals | Ethers | Hydrogen bonding | Alcohols
Journal Article
Synlett, ISSN 0936-5214, 03/2018, Volume 29, Issue 5, pp. 609 - 612
Abstract A concise approach to the total syntheses of racemic paniculidines B and C is described. The route features a combined Tamaru allylation/olefin... 
letter | prenylindoles | total synthesis | cross-metathesis | carbazoles | Tamaru allylation | alkaloids
Journal Article
ACS catalysis, ISSN 2155-5435, 08/2017, Volume 7, Issue 8, pp. 5443 - 5449
The active species generated from ruthenium complexes bearing N-heterocyclic carbene (NHC) ligands exhibit limited stability under certain conditions (high... 
carbenes | ruthenium | renewable resources | metathesis | cross metathesis | Physical Sciences | Chemistry | Chemistry, Physical | Science & Technology
Journal Article
Chemistry : a European journal, ISSN 0947-6539, 10/2014, Volume 20, Issue 41, pp. 13188 - 13193
Terminal acetylenes are amongst the most problematic substrates for alkyne metathesis because they tend to undergo rapid polymerization on contact with a metal... 
alkylidynes | protecting groups | cross‐metathesis | alkynes | molybdenum | Cross-metathesis | Alkylidynes | Molybdenum | Protecting groups | Alkynes | cross-metathesis | Polymerization | Silane | Acetylene | Catalysts | Aromatic compounds | Decomposition reactions | Transformations | Terminals
Journal Article
Synthesis, ISSN 0039-7881, 03/2015, Volume 47, Issue 6, pp. 845 - 853
Abstract Synthesis of the C13–C28 fragment of marinomycin A, consisting of all the five stereocenters, was achieved by asymmetric synthesis, starting from l... 
paper | Hoveyda-Grubbs | cross-metathesis | stereoselective | marinomycins
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 08/2013, Volume 52, Issue 32, pp. 8395 - 8400
Journal Article
Synlett, ISSN 1437-2096, 10/2014, Volume 25, Issue 18, pp. 2624 - 2628
Abstract An efficient approach to a new family of highly functionalized P analogues of α-trifluoromethyl-substituted phenylalanine and its homologues using... 
letter | catalysis | cross-metathesis | diynes | aminophosphonates | alkynes | Chemical Sciences | Catalysis
Journal Article
Synthesis, ISSN 0039-7881, 03/2014, Volume 46, Issue 6, pp. 822 - 827
Abstract Asymmetric total synthesis of α-isomers of ieodoglucomides A and B along with their C14-epimers has been achieved starting from d -glucose. The key... 
paper | glycosylation | glycolipids | cross-metathesis | stereoisomer | cytotoxicity
Journal Article
Synthesis, ISSN 0039-7881, 04/2016, Volume 48, Issue 8, pp. 1181 - 1190
Abstract A modular synthesis of some cyclic peptides related to a class of histone deacetylase inhibitors is reported. The synthesis utilizes a late-stage... 
paper | modular synthesis | catalysis | peptides | cross metathesis | macrocycles
Journal Article
Synthesis, ISSN 0039-7881, 03/2016, Volume 48, Issue 6, pp. 917 - 923
Abstract This communication describes the synthesis of the fully functionalized C1 to C13 segment (southern part) of highly potent cytotoxic marine natural... 
paper | cross-metathesis | mandelalide | modified Takai olefination | oxa-Michael cyclization
Journal Article
Macromolecular chemistry and physics, ISSN 1022-1352, 05/2018, Volume 219, Issue 10, pp. 1800031 - n/a
Journal Article
Synthesis, ISSN 0039-7881, 02/2019, Volume 51, Issue 3, pp. 780 - 786
Abstract The total synthesis of 5-hydroxygoniothalamin is achieved from commercially available l -xylose. The α,β-unsaturated-δ-lactone core is constructed in... 
paper | C2 Wittig reaction | C1 Wittig reaction | Yamaguchi reaction | cross-metathesis | 5-hydroxygoniothalamin
Journal Article
Journal of polymer science. Part A, Polymer chemistry, ISSN 0887-624X, 07/2018, Volume 56, Issue 14, pp. 1584 - 1592
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 04/2015, Volume 54, Issue 17, pp. 5018 - 5024
Olefin cross metathesis is a particularly powerful transformation that has been exploited extensively for the formation of complex products. Until recently,... 
olefin metathesis | natural products | Z‐alkenes | cross metathesis | Z-alkenes | Cross metathesis | Olefin metathesis | Natural products | Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology | Ruthenium | Catalysts | Olefins | Decomposition reactions | Metathesis | Alkylidene | Formations | Terminals | Catalysis
Journal Article