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Chackalamannil Samuel
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http://hub.abes.fr/acs/periodical/joceah/1983/volume_48/issue_20/101021jo00168a067/authorship/2
http://hub.abes.fr/acs/periodical/ancham/2003/volume_75/issue_8/101021ac020630e/authorship/4
http://hub.abes.fr/acs/periodical/joceah/2000/volume_65/issue_17/101021jo991928g/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_21/101021jm070704k/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_8/101021jm701519h/authorship/4
http://hub.abes.fr/acs/periodical/jmcmar/2002/volume_45/issue_25/101021jm0255163/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_18/101021jm0603670/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_19/101021jm0502236/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_1/101021jm061043e/authorship/2
http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_4/101021jo0160322/authorship/6
http://hub.abes.fr/acs/periodical/jacsat/2006/volume_128/issue_39/101021ja065198n/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_11/101021jm800180e/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1982/volume_47/issue_26/101021jo00147a020/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/1985/volume_107/issue_8/101021ja00294a046/authorship/2
http://hub.abes.fr/acs/periodical/joceah/1982/volume_47/issue_11/101021jo00132a064/authorship/2
http://hub.abes.fr/acs/periodical/joceah/1988/volume_53/issue_2/101021jo00237a050/authorship/1
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Synthetic studies toward aflavinine: a synthesis of 3-demethylaflavinine via a [2 + 2 + 2] annulation
An efficient synthesis of (3R,4R)-3-(1-(R)-hydroxyethyl)-4-(benzoyloxy)-2-azetidinone from L-threonine. Use of phenylalkoxymethyl as a novel N-protecting group
Reductive cyclization of mercurial enones
Heterotricyclic Himbacine Analogs as Potent, Orally Active Thrombin Receptor (ProteaseActivated Receptor-1) Antagonists
Discovery of a Novel, Orally Active Himbacine-Based Thrombin Receptor Antagonist (SCH 530348) with Potent Antiplatelet Activity
Direct Plasma Analysis of Drug Compounds UsingMonolithic Column Liquid Chromatography andTandem Mass Spectrometry
Total Synthesis of (−)-Himgaline
Stereochemistry of the Oxidation of Imines Derived fromSubstituted Cyclohexanones: Axial vs Equatorial Attack andEvidence for Delivery by an Adjacent Hydroxyl Group
Discovery of Potent Orally ActiveThrombin Receptor (Protease ActivatedReceptor 1) Antagonists as NovelAntithrombotic Agents
Thrombin Receptor (Protease Activated Receptor-1) Antagonists as Potent AntithromboticAgents with Strong Antiplatelet Effects
Synthesis of Mono- and Difluoronaphthoic Acids
Improving the Oral Efficacy of CNS DrugCandidates: Discovery of Highly OrallyEfficacious Piperidinyl Piperidine M2Muscarinic Receptor Antagonists
Metabolism-Based Identification of a Potent Thrombin Receptor Antagonist
Identification of Novel Cannabinoid CB1 Receptor Antagonists by Using Virtual Screening with a Pharmacophore Model
Stereospecific 2 + 2 + 2 annulation
Hofmann degradation of .beta.-hydroxy ammonium salts. .alpha.- and .beta.-Hydroxylaudanosine, 7-hydroxyglaucine, and 13-hydroxyxylopinine
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