| Introducing “ynene” metathesis: ring-expansion metathesis polymerization leads to highly cis and syndiotactic cyclic polymers of norbornene SS Nadif, T Kubo, SA Gonsales, S VenkatRamani, I Ghiviriga, ... Journal of the American Chemical Society 138 (20), 6408-6411, 2016 | 84 | 2016 |
| An easily accessible Re-based catalyst for the selective conversion of methanol: Evidence for an unprecedented active site structure through combined operando techniques A Yoboué, A Susset, A Tougerti, D Gallego, SV Ramani, M Kalyanikar, ... Chemical communications 47 (14), 4285-4287, 2011 | 24 | 2011 |
| A catalytically relevant intermediate in the synthesis of cyclic polymers from alkynes CD Roland, T Zhang, S VenkatRamani, I Ghiviriga, AS Veige Chemical Communications 55 (91), 13697-13700, 2019 | 23 | 2019 |
| Synthesis and Characterization of a Molybdenum Alkylidyne Supported by a Trianionic OCO3– Pincer Ligand CD Roland, S VenkatRamani, VK Jakhar, I Ghiviriga, KA Abboud, ... Organometallics 37 (23), 4500-4505, 2018 | 19 | 2018 |
| Syntheses of Molybdenum Adamantylimido and t-Butylimido Alkylidene Chloride Complexes Using HCl and Diphenylmethylphosphine KV Bukhryakov, S VenkatRamani, C Tsay, A Hoveyda, RR Schrock Organometallics 36 (21), 4208-4214, 2017 | 18 | 2017 |
| Trianionic pincer complexes of niobium and tantalum as precatalysts for ROMP of norbornene S VenkatRamani, CD Roland, JG Zhang, I Ghiviriga, KA Abboud, ... Organometallics 35 (16), 2675-2682, 2016 | 17 | 2016 |
| A new ONO 3− trianionic pincer ligand with intermediate flexibility and its tungsten alkylidene and alkylidyne complexes S VenkatRamani, I Ghiviriga, KA Abboud, AS Veige Dalton Transactions 44 (42), 18475-18486, 2015 | 17 | 2015 |
| Single versus double Cu (I) catalyzed [3+ 2] azide/platinum diacetylide cycloaddition reactions X Yang, S VenkatRamani, CC Beto, TJ Del Castillo, I Ghiviriga, ... Organometallics 36 (7), 1352-1357, 2017 | 13 | 2017 |
| New Alkylidyne Complexes Featuring a Flexible Trianionic ONO3– Pincer-Type Ligand: Inorganic Enamine Effect versus Sterics in Electrophilic Additions S VenkatRamani, NB Huff, MT Jan, I Ghiviriga, KA Abboud, AS Veige Organometallics 34 (12), 2841-2848, 2015 | 13 | 2015 |
| Synthesis and characterization of trianionic pincer-type complexes of tantalum (V) including solid (X-ray) and solution (NMR) state assignment of an intraligand N–H—F hydrogen … S VenkatRamani, ME Pascualini, I Ghiviriga, KA Abboud, AS Veige Polyhedron 64, 377-387, 2013 | 12 | 2013 |
| Synthesis of tungsten oxo alkylidene biphenolate complexes and ring-opening metathesis polymerization of norbornenes and norbornadienes T Yan, S VenkatRamani, RR Schrock, P Müller Organometallics 38 (16), 3144-3150, 2019 | 11 | 2019 |
| Synthesis of High-Oxidation-State Mo═CHX Complexes, Where X = Cl, CF3, Phosphonium, CN S VenkatRamani, RR Schrock, AH Hoveyda, P Müller, C Tsay Organometallics 37 (11), 1641-1644, 2018 | 9 | 2018 |
| Synthesis and Characterization of Tungsten Alkylidene and Alkylidyne Complexes Featuring a New Carbazole-Based Rigid Trianionic ONO3– Pincer-Type Ligand U Mandal, S VenkatRamani, I Ghiviriga, KA Abboud, AS Veige Organometallics 39 (12), 2207-2213, 2020 | 6 | 2020 |
| Syntheses of Molybdenum and Tungsten Imido Alkylidene Complexes that Contain a Bidentate Oxo/Thiolato Ligand H Tafazolian, S VenkatRamani, C Tsay, RR Schrock, P Müller Helvetica Chimica Acta 103 (6), e2000068, 2020 | 1 | 2020 |
| Syntheses of Molybdenum and Tungsten Imido Alkylidene Complexes that Contain a H Tafazolian, S VenkatRamani, C Tsay | | 2020 |
| Synthesis of high oxidation state Mo= CHX complexes (X= Cl, CF3, CN) relevant to Z-selective electron poor olefin metathesis S VenkatRamani, K Bukhryakov, R Schrock, A Hoveyda, C Tsay, ... ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY 256, 2018 | | 2018 |
| Dialkyl Complexes of Ta and Nb supported by the [CF3-ONO] 3-trianionic pincer ligand and ROMP of norbornene S VenkatRamani, I Ghiviriga, K Abboud, A Veige ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY 252, 2016 | | 2016 |
Adam Steven VeigeUniversity of Florida確認したメール アドレス: chem.ufl.edu
