Basic concepts in organic stereochemistry / / Sunil Kumar Talapatra, Bani Talapatra
| Basic concepts in organic stereochemistry / / Sunil Kumar Talapatra, Bani Talapatra |
| Autore | Talapatra Sunil Kumar |
| Edizione | [1st ed. 2022.] |
| Pubbl/distr/stampa | Cham, Switzerland : , : Springer, , [2022] |
| Descrizione fisica | 1 online resource (266 pages) |
| Disciplina | 547.1223 |
| Soggetto topico | Stereochemistry |
| ISBN | 3-030-95990-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Symmetry and Molecular Chirality. Conformation, Stability, and Physical Properties -- Configurational Nomenclature. Physical Properties of Geometrical Isomers -- Projection (Fischer, Newman, Sawhorse) and Perspective (Flying Wedge and Zigzag) Formulas, Working out Stereoisomers -- Prochirality and Prostereoisomerism. Topicity of Ligands and Faces Nomenclature [1–5] -- Asymmetric Synthesis -- Some Other Aspects of Dynamic Stereochemistry: Conformation and Reactivity -- Conformation of Saturated Six-Membered Ring Compounds -- Cyclohexanone -- Fused Ring Systems -- Stereoisomerism: Axial Chirality, Planar Chirality, (R,S) Notations Helicity -- Chiroptical Properties I: Optical Rotation. ORD, CD [1-4] -- Chiroptical Properties II: Helicity Rule or Chirality Rule. |
| Record Nr. | UNINA-9910637715803321 |
Talapatra Sunil Kumar
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| Cham, Switzerland : , : Springer, , [2022] | ||
| Lo trovi qui: Univ. Federico II | ||
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Chemistry of Plant Natural Products : Stereochemistry, Conformation, Synthesis, Biology, and Medicine / / by Sunil Kumar Talapatra, Bani Talapatra
| Chemistry of Plant Natural Products : Stereochemistry, Conformation, Synthesis, Biology, and Medicine / / by Sunil Kumar Talapatra, Bani Talapatra |
| Autore | Talapatra Sunil Kumar |
| Edizione | [1st ed. 2015.] |
| Pubbl/distr/stampa | Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2015 |
| Descrizione fisica | 1 online resource (1196 p.) |
| Disciplina | 547.7 |
| Soggetto topico |
Chemistry, Organic
Pharmaceutical chemistry Pharmacology Biochemistry Pharmacy Organic Chemistry Medicinal Chemistry Pharmacology/Toxicology Biochemistry, general |
| ISBN | 3-642-45410-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Introduction: enzymes, cofactors/coenzymes, primary and secondary metabolites, natural products and their functions, plant chemical ecology, biosynthesis, metabolic pathways -- Fundamental Stereochemical Concepts and Nomenclatures -- Important Biological Events Occurring in Plants -- Natural Products Chemistry -- Biosynthesis of Terpenoids, The Oldest Natural Products -- Monoterpenoids (C10) -- Sesquiterpenoids (C15) -- Diterpenoids (C20) -- Sesterpenoids (C25) -- Triterpenes -- Steroids: Cholesterol and Other Phytosterols -- Carotenoids-GGPP Derived Polyisoprenoid (C40) Coloring Pigments -- Shikimic Acid Pathway -- Polyketide Pathway, Biosynthesis of Diverse Clases of Aromatic Compounds -- Alkaloids: General Introduction -- Hygrine, Hygroline and Cuscohygrine (Ornithine-Derived Alkaloids) -- Coniine, Conhydrine and Pseudoconhydrine -- Nicotine -- Atropine [(±)-Hyoscyamine] and Cocaine -- Ephedrine and Pseudoephedrine -- Pilocarpine and Isopilocarpine -- Papaverine -- Morphine, Codeine, Thebaine -- Colchicine -- Quinine: Cinchona Alkalods -- Reserpine -- Strychnine, an Alkaloid with Heptacyclic Dense Molecular Scaffold -- Dimeric Indole Alkaloids:Vinblastine (Vincaleukoblastine), Vineristine (Leurocristine) and Their Derivatives -- Some More Alkaloids Having Diverse Skeletal Patterns -- Important Outcomes of Chemical Studies on Natural Products -- Chiral Recognition in Biological Systems and Natural Chiral Auxiliaries -- Natural Products in the Parlor of Pharmaceuticals -- Organic Phytonutrients and Their Functions -- Appendices. . |
| Record Nr. | UNINA-9910298628003321 |
Talapatra Sunil Kumar
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| Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2015 | ||
| Lo trovi qui: Univ. Federico II | ||
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