International Union of Pure and Applied Chemistry
-
Tomislav Rovis
and John Montgomery
Held in Fort Collins, CO, USA
28 July–1 August 2013
Conference Editor
John Montgomery
Department of Chemistry, University of Michigan, Ann Arbor, MI 48109-1055, USA
International Advisory Committee: A. Alexakis (Switzerland); P. Dixneuf (France); J.-P. Genet (France); R. W. Hoffmann (Germany); E. Peter Kündig (Switzerland); P. Kocovsky (Scotland); M. Lautens (Canada); B. Lipshutz (USA); K. Oshima (Japan); T.-Y. Luh (Taiwan); S. Ma (China); A. de Meijere (Germany); S.-I. Murahashi (Japan); G. van Koten (Netherlands).
The 17th International Symposium on Organometallic Chemistry Directed Towards Organic Synthesis (OMCOS-17) was held in Fort Collins, CO, USA on the outskirts of the campus of Colorado State University from 28 July to 1 August 2013. This event marked the return of OMCOS to Fort Collins following the launch of this conference series in Fort Collins in 1981 with OMCOS-1. The original OMCOS meeting was organized by Louis S. Hegedus and the late John K. Stille, and we were fortunate in the opening reception to hear remarks from Lou reminiscing about the original event. These opening remarks were of course very candid and entertaining, which comes as no surprise to those who know Lou. Following the original meeting, OMCOS has been held every other year, with meetings in Dijon (1983), Kyoto (1985), Vancouver (1987), Florence (1989), Utrecht (1991), Kobe (1993), Santa Barbara (1985), Göttingen (1997), Versailles (1999), Taipei (2001), Toronto (2003), Geneva (2005), Nara (2007), Glasgow (2009), and Shanghai (2011).
The symposium attracted 550 attendees from 40 countries across the globe. There were two award lectures presented: the OMCOS Award to Zhang-Jie Shi and the EROS Award to Huw Davies. Additionally, there were seven plenary lectures, 12 invited lectures, 12 short talks, and 347 posters. Twenty poster awards were presented, which was far too few given the superb quality of the work presented. There were fantastic excursions planned during the week, and the world-class Fort Collins microbreweries reported a marked uptake in local consumption during the event.
This issue of Pure and Applied Chemistry comprises a collection of 17 papers based on the lectures presented at OMCOS-17, thereby offering the readers a glimpse of the fascinating achievements communicated at the symposium.
We look forward to the exciting science and spectacular setting of OMCOS-18, which will be held in 2015 in Sitges, Spain, located on the Mediterranean coast south of Barcelona. The meeting will be hosted by the Institute of Chemical Research of Catalonia (ICIQ) under the leadership of Antonio Echavarren, Rubén Martín, and Kilian Muñiz. For details, please see: http://www.omcos2015.com.
©2014 by IUPAC & De Gruyter
Articles in the same Issue
- Masthead
- Masthead
- Conference papers
- International Union of Pure and Applied Chemistry
- Enantioselective palladium(0)-catalyzed C–H arylation strategy for chiral heterocycles
- Organometallic catalysis for applications in radical chemistry and asymmetric synthesis
- Rhenium(I)-catalyzed reaction of terminal alkynes with imines leading to allylamine derivatives
- Copper-catalyzed aminoboration and hydroamination of alkenes with electrophilic amination reagents
- Activation of stable σ-bonds for organic synthesis
- Pd-catalyzed reactions of unactivated Csp3−I bonds
- Pd- and Ni-catalyzed C–H arylations using C–O electrophiles
- Nickel-catalyzed oxidative cross-coupling of arylboronic acids with olefins
- Stereoselective C-glycosylation of furanosyl halides with arylzinc reagents
- Transition-metal clusters as catalysts for chemoselective transesterification of alcohols in the presence of amines
- Cu(I)/Cu(III) catalytic cycle involved in Ullmann-type cross-coupling reactions
- Beyond C–H and C–O activation: the evolution of components in cross-coupling reactions
- The effect of acceptor-substituted alkynes in gold-catalyzed intermolecular reactions
- Chemoselective silver-catalyzed nitrene insertion reactions
- The strategic generation and interception of palladium-hydrides for use in alkene functionalization reactions
- 3-Acyloxy-1,4-enyne: A new five-carbon synthon for rhodium-catalyzed [5 + 2] cycloadditions
- Cobalt-catalyzed directed alkylation of arenes with primary and secondary alkyl halides
- IUPAC Technical Report
- Assessment of international reference materials for isotope-ratio analysis (IUPAC Technical Report)
Articles in the same Issue
- Masthead
- Masthead
- Conference papers
- International Union of Pure and Applied Chemistry
- Enantioselective palladium(0)-catalyzed C–H arylation strategy for chiral heterocycles
- Organometallic catalysis for applications in radical chemistry and asymmetric synthesis
- Rhenium(I)-catalyzed reaction of terminal alkynes with imines leading to allylamine derivatives
- Copper-catalyzed aminoboration and hydroamination of alkenes with electrophilic amination reagents
- Activation of stable σ-bonds for organic synthesis
- Pd-catalyzed reactions of unactivated Csp3−I bonds
- Pd- and Ni-catalyzed C–H arylations using C–O electrophiles
- Nickel-catalyzed oxidative cross-coupling of arylboronic acids with olefins
- Stereoselective C-glycosylation of furanosyl halides with arylzinc reagents
- Transition-metal clusters as catalysts for chemoselective transesterification of alcohols in the presence of amines
- Cu(I)/Cu(III) catalytic cycle involved in Ullmann-type cross-coupling reactions
- Beyond C–H and C–O activation: the evolution of components in cross-coupling reactions
- The effect of acceptor-substituted alkynes in gold-catalyzed intermolecular reactions
- Chemoselective silver-catalyzed nitrene insertion reactions
- The strategic generation and interception of palladium-hydrides for use in alkene functionalization reactions
- 3-Acyloxy-1,4-enyne: A new five-carbon synthon for rhodium-catalyzed [5 + 2] cycloadditions
- Cobalt-catalyzed directed alkylation of arenes with primary and secondary alkyl halides
- IUPAC Technical Report
- Assessment of international reference materials for isotope-ratio analysis (IUPAC Technical Report)