Search Results - "Turpin, Victor"

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    Bioinspired Oxidative Cyclization of the Geissoschizine Skeleton for Enantioselective Total Synthesis of Mavacuran Alkaloids by Jarret, Maxime, Turpin, Victor, Tap, Aurélien, Gallard, Jean‐François, Kouklovsky, Cyrille, Poupon, Erwan, Vincent, Guillaume, Evanno, Laurent

    Published in Angewandte Chemie International Edition (15-07-2019)
    “…Reported is the enantioselective total syntheses of mavacuran alkaloids, (+)‐taberdivarine H, (+)‐16‐hydroxymethyl‐pleiocarpamine, and…”
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    Journal Article
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    OceanGliders: A Component of the Integrated GOOS by Testor, Pierre, de Young, Brad, Rudnick, Daniel L., Glenn, Scott, Hayes, Daniel, Lee, Craig M., Pattiaratchi, Charitha, Hill, Katherine, Heslop, Emma, Turpin, Victor, Alenius, Pekka, Barrera, Carlos, Barth, John A., Beaird, Nicholas, Bécu, Guislain, Bosse, Anthony, Bourrin, François, Brearley, J. Alexander, Chao, Yi, Chen, Sue, Chiggiato, Jacopo, Coppola, Laurent, Crout, Richard, Cummings, James, Curry, Beth, Curry, Ruth, Davis, Richard, Desai, Kruti, DiMarco, Steve, Edwards, Catherine, Fielding, Sophie, Fer, Ilker, Frajka-Williams, Eleanor, Gildor, Hezi, Goni, Gustavo, Gutierrez, Dimitri, Haugan, Peter, Hebert, David, Heiderich, Joleen, Henson, Stephanie, Heywood, Karen, Hogan, Patrick, Houpert, Loïc, Huh, Sik, E. Inall, Mark, Ishii, Masso, Ito, Shin-ichi, Itoh, Sachihiko, Jan, Sen, Kaiser, Jan, Karstensen, Johannes, Kirkpatrick, Barbara, Klymak, Jody, Kohut, Josh, Krahmann, Gerd, Krug, Marjolaine, McClatchie, Sam, Marin, Frédéric, Mauri, Elena, Mehra, Avichal, P. Meredith, Michael, Meunier, Thomas, Miles, Travis, Morell, Julio M., Mortier, Laurent, Nicholson, Sarah, O'Callaghan, Joanne, O'Conchubhair, Diarmuid, Oke, Peter, Pallàs-Sanz, Enric, Palmer, Matthew, Park, JongJin, Perivoliotis, Leonidas, Poulain, Pierre-Marie, Perry, Ruth, Queste, Bastien, Rainville, Luc, Rehm, Eric, Roughan, Moninya, Rome, Nicholas, Ross, Tetjana, Ruiz, Simon, Saba, Grace, Schaeffer, Amandine, Schönau, Martha, Schroeder, Katrin, Shimizu, Yugo, Sloyan, Bernadette M., Smeed, David, Snowden, Derrick, Song, Yumi, Swart, Sebastian, Tenreiro, Miguel, Thompson, Andrew, Tintore, Joaquin, Todd, Robert E., Toro, Cesar, Venables, Hugh, Wagawa, Taku, Waterman, Stephanie

    Published in Frontiers in Marine Science (02-10-2019)
    “…The OceanGliders program started in 2016 to support active coordination and enhancement of global glider activity. OceanGliders contributes to the…”
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    Journal Article
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    Best practices for Core Argo floats - part 1: getting started and data considerations by Morris, Tamaryn, Scanderbeg, Megan, West-Mack, Deborah, Gourcuff, Claire, Poffa, Noé, Bhaskar, T. V. S. Udaya, Hanstein, Craig, Diggs, Steve, Talley, Lynne, Turpin, Victor, Liu, Zenghong, Owens, Breck

    Published in Frontiers in Marine Science (27-03-2024)
    “…Argo floats have been deployed in the global ocean for over 20 years. The Core mission of the Argo program (Core Argo) has contributed well over 2 million…”
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    Best practices for Core Argo floats - Part 2: physical handling, deployment and metadata considerations by Morris, Tamaryn, Scanderbeg, Megan, West-Mack, Deborah, Gourcuff, Claire, Poffa, Noé, Udaya Bhaskar, Tata V. S., Hanstein, Craig, Diggs, Steve, Talley, Lynne, Turpin, Victor, Liu, Zenghong, Owens, Breck

    Published in Frontiers in Marine Science (03-04-2024)
    “…Following on from Part 1: Best Practices for Core Argo floats - Getting started and data considerations, we present Part 2: Best Practices for Core Argo floats…”
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    Journal Article
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    Corrigendum: OceanGliders: A Component of the Integrated GOOS by Testor, Pierre, Young, Brad de, Rudnick, Daniel L., Glenn, Scott, Hayes, Daniel, Lee, Craig M., Pattiaratchi, Charitha, Hill, Katherine, Heslop, Emma, Turpin, Victor, Alenius, Pekka, Barrera, Carlos, Barth, John A., Beaird, Nicholas, Bécu, Guislain, Bosse, Anthony, Bourrin, François, Brearley, J. Alexander, Chao, Yi, Chen, Sue, Chiggiato, Jacopo, Coppola, Laurent, Crout, Richard, Cummings, James, Curry, Beth, Curry, Ruth, Davis, Richard, Desai, Kruti, DiMarco, Steve, Edwards, Catherine, Fielding, Sophie, Fer, Ilker, Frajka-Williams, Eleanor, Gildor, Hezi, Goni, Gustavo, Gutierrez, Dimitri, Haugan, Peter, Hebert, David, Heiderich, Joleen, Henson, Stephanie, Heywood, Karen, Hogan, Patrick, Houpert, Loïc, Huh, Sik, Inall, Mark E., Ishii, Masso, Ito, Shin-ichi, Itoh, Sachihiko, Jan, Sen, Kaiser, Jan, Karstensen, Johannes, Kirkpatrick, Barbara, Klymak, Jody, Kohut, Josh, Krahmann, Gerd, Krug, Marjolaine, McClatchie, Sam, Marin, Frédéric, Mauri, Elena, Mehra, Avichal, Meredith, Michael P., Meunier, Thomas, Miles, Travis, Morell, Julio M., Mortier, Laurent, Nicholson, Sarah, O'Callaghan, Joanne, O'Conchubhair, Diarmuid, Oke, Peter, Pallàs-Sanz, Enric, Palmer, Matthew, Park, JongJin, Perivoliotis, Leonidas, Poulain, Pierre-Marie, Perry, Ruth, Queste, Bastien, Rainville, Luc, Rehm, Eric, Roughan, Moninya, Rome, Nicholas, Ross, Tetjana, Ruiz, Simon, Saba, Grace, Schaeffer, Amandine, Schönau, Martha, Schroeder, Katrin, Shimizu, Yugo, Sloyan, Bernadette M., Smeed, David, Snowden, Derrick, Song, Yumi, Swart, Sebastian, Tenreiro, Miguel, Thompson, Andrew, Tintore, Joaquin, Todd, Robert E., Toro, Cesar, Venables, Hugh, Wagawa, Taku, Waterman, Stephanie

    Published in Frontiers in Marine Science (24-05-2021)
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    Journal Article
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    Biosynthetically Relevant Reactivity of Polyneuridine Aldehyde by Turpin, Victor, Poupon, Erwan, Jullian, Jean‐Christophe, Evanno, Laurent

    Published in European journal of organic chemistry (07-12-2020)
    “…Polyneuridine aldehyde is a key intermediate in the biosynthetic routes of monoterpene indole alkaloids family of natural products. The molecule is the first…”
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    In Silico Anticipation of Metabolic Pathways Extended to Organic Chemistry Reactions: A Case Study with Caffeine Alkaline Hydrolysis and The Origin of Camellimidazoles by Turpin, Victor, Beniddir, Mehdi, Genta-Jouve, Grégory, Skiredj, Adam, Gallard, Jean‐françois, Leblanc, Karine, Le Pogam, Pierre, Poupon, Erwan

    Published in Chemistry : a European journal (17-09-2020)
    “…Abstract Camellimidazoles A–C were recently reported as natural substances in Keemun black tea. Although a “biosynthetic” route to these intriguing imidazole…”
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    Journal Article
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    In Silico Anticipation of Metabolic Pathways Extended to Organic Chemistry Reactions: A Case Study with Caffeine Alkaline Hydrolysis and The Origin of Camellimidazoles by Turpin, Victor, Beniddir, Mehdi A., Genta‐Jouve, Grégory, Skiredj, Adam, Gallard, Jean‐François, Leblanc, Karine, Le Pogam, Pierre, Poupon, Erwan

    Published in Chemistry : a European journal (09-10-2020)
    “…Camellimidazoles A–C were recently reported as natural substances in Keemun black tea. Although a “biosynthetic” route to these intriguing imidazole dimers was…”
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    Journal Article
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    The CORA dataset: validation and diagnostics of in-situ ocean temperature and salinity measurements by Cabanes, C, Grouazel, A, von Schuckmann, K, Hamon, M, Turpin, V, Coatanoan, C, Paris, F, Guinehut, S, Boone, C, Ferry, N, de Boyer Montégut, C, Carval, T, Reverdin, G, Pouliquen, S, Le Traon, P.-Y

    Published in Ocean science (10-01-2013)
    “…The French program Coriolis, as part of the French operational oceanographic system, produces the COriolis dataset for Re-Analysis (CORA) on a yearly basis…”
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    Bioinspired Oxidative Cyclization of the Geissoschizine Skeleton for Enantioselective Total Synthesis of Mavacuran Alkaloids by Jarret, Maxime, Turpin, Victor, Tap, Aurélien, Gallard, Jean‐François, Kouklovsky, Cyrille, Poupon, Erwan, Vincent, Guillaume, Evanno, Laurent

    Published in Angewandte Chemie (15-07-2019)
    “…Reported is the enantioselective total syntheses of mavacuran alkaloids, (+)‐taberdivarine H, (+)‐16‐hydroxymethyl‐pleiocarpamine, and…”
    Get full text
    Journal Article
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    How essential are Argo observations to constrain a global ocean data assimilation system? by Turpin, V, Remy, E, Le Traon, P. Y

    Published in Ocean science (16-02-2016)
    “…Observing system experiments (OSEs) are carried out over a 1-year period to quantify the impact of Argo observations on the Mercator Ocean 0.25° global ocean…”
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    Journal Article
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