1 - 1 |
16th International Symposium on Olefin Metathesis and Related Chemistry - Preface Marciniec B |
2 - 19 |
Ring closing metathesis employing organometallic substrates and the templated synthesis of macrocycles Chase PA, Lutz M, Spek AL, van Klink GPM, van Koten G |
20 - 28 |
Generation of trans-spanning diphosphine ligands via alkene metathesis: Synthesis, structure, and dynamic behavior of a missing link in a series of square-planar platinum complexes Lewanzik N, Oeser T, Blumel J, Gladysz JA |
29 - 42 |
Metal carbenes in enyne metathesis: Synthetic and mechanistic studies Diver ST |
43 - 52 |
Application of ring closing metathesis in efficient synthesis of macrocyclic crown compounds Ibrahim YA |
53 - 57 |
Olefin metathesis and isomerization: From undesired side reactions to useful synthetic methodology Schmidt B |
58 - 63 |
Highly stereoselective synthesis of E-4-chlorostilbene and its derivatives via tandem cross-metathesis (or silylative coupling) and Hiyama coupling Prukala W, Majchrzak M, Pietraszuk C, Marciniec B |
64 - 67 |
ROM-RCM of azabicycloheptene derivatives - Study of products distribution by the substituent on alkyne Mori M, Wakamatsu H, Sato Y, Fujita R |
68 - 77 |
Alkene- and alkyne-bridged mimics of nisin as potential peptide-based antibiotics Ghalit N, Rijkers DTS, Liskamp RMJ |
78 - 84 |
Exploiting catalyst characteristics: A protocol for increasing diastereoselectivity in a double ring-closing metathesis reaction Wallace DJ |
85 - 92 |
Alkoxy group facilitated ring closing metathesis (RCM) of acyclic 1,6-dienes - Facile synthesis of non-racemic highly substituted cyclopentenols Banerjee S, Nayek A, Sinha S, Bhaumik T, Ghosh S |
93 - 95 |
Unsymmetrical maleates from stereoselective decomposition of diazoesters using Grubbs' 2nd-generation Ru carbene catalyst Hodgson DM, Angrish D |
96 - 104 |
Alkyne metathesis catalysts: Scope and future Mortreux A, Coutelier O |
105 - 110 |
Ruthenium aryloxide catalysts: Synthesis and applications in ring-closing metathesis Conrad JC, Snelgrove JL, Eeelman MD, Hall S, Fogg DE |
111 - 117 |
The utility of Hoveyda-type catalysts in ADMET chemistry: Sterics versus electronics Courchay FC, Sworen JC, Coronado A, Wagener KB |
118 - 123 |
New tunable catalysts for olefin metathesis: Controlling the initiation through electronic factors Gulajski L, Michrowska A, Bujok R, Grela K |
124 - 130 |
Nitrogen ligand-containing Rh catalysts for the polymerization of substituted acetylenes Saeed I, Shiotsuki M, Masuda T |
131 - 137 |
Preparation and characterization of iminopyrrolyl hafnium complexes as catalyst precursors for alpha-olefin polymerization Tsurugi H, Matsuo Y, Mashima K |
138 - 144 |
Supporting ruthenium initiator on PolyHIPE Cetinkaya S, Khosravi E, Thompson R |
145 - 154 |
Experimental and DFT investigation of the 1-octene metathesis reaction mechanism with the Grubbs 1 precatalyst Jordaan M, van Helden P, van Sittert CGCE, Vosloo HCM |
155 - 164 |
Recent mechanistic developments in atom transfer radical polymerization Braunecker WA, Matyjaszewski K |
165 - 173 |
In situ NMR investigations into the ADMET-reaction of 1,4-diheptyloxy-2,5-divinylbenzene via a Schrock-type molybdenum alkylidene complex Peetz RM, Sinnwell V, Thorn-Csanyi E |
174 - 179 |
Photosensitive polynorbornene containing the benzyl thiocyanate group -Synthesis and patterning Lex A, Trimmel G, Kern W, Stelzer F |
180 - 185 |
Qualitative FT-Raman investigation of the ring opening metathesis polymerization of dicyclopentadiene Schaubroeck D, Brughmans S, Vercaemst C, Schaubroeck J, Verpoort F |
186 - 191 |
Synthesis and characterization of Ge- and Sn-containing ADMET polymers Solmaz K, Cemil A, Bulent D, Imamoglu Y |
192 - 196 |
Effect of phenoxy ligands on catalytic properties of titanium half-sandwich complexes/MAO systems Jamanek D, Nicinski K, Kazimierczuk R, Wozniewski T, Wieczorek Z, Skupinski W |
197 - 205 |
Effect of aryloxide ligand in 1-hexene, styrene polymerization catalyzed by nonbridged half-titanocenes of the type, Cp' TiCl2(OAr) (Cp' = C5Me5, (BuC5H4)-Bu-t) - Structural analyses for Cp*TiCl2(O-2,6-(Bu2C6H3)-Bu-t) and Cp*TiCl2(O-2,6-Pr-i(2)-4-(BuC6H2)-Bu-t) Nomura K, Tanaka A, Katao S |