{"product_id":"advanced-organic-chemistry-ii-pharmaceutical-chemistry-m-pharm-second-semester-authors-dr-p-sivakumar-prof-dr-m-sivagamy-dr-m-senthilraja-thakur-publications-pvt-ltd","title":"ADVANCED ORGANIC CHEMISTRY-II (PHARMACEUTICAL CHEMISTRY) M.PHARM SECOND SEMESTER,Authors : Dr. P. Sivakumar, (Prof.) Dr. M. Sivagamy, Dr. M. Senthilraja,  THAKUR PUBLICATIONS PVT LTD","description":"\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"Style3\"\u003e\u003ci\u003e\u003cspan\u003eSyllabus\u003c\/span\u003e\u003c\/i\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\" align=\"center\"\u003e\u003cspan\u003e \u003c\/span\u003e\u003c\/p\u003e\n\u003cp class=\"MsoNormal\" align=\"center\"\u003e\u003cb\u003e\u003cspan lang=\"en-in\"\u003eMPC 202T\u003c\/span\u003e\u003c\/b\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\" align=\"center\"\u003e\u003cb\u003e\u003cspan lang=\"en-in\"\u003eAdvanced Organic Chemistry – II\u003c\/span\u003e\u003c\/b\u003e\u003cspan lang=\"en-in\"\u003e\u003c\/span\u003e\u003cb\u003e\u003cspan lang=\"en-in\"\u003e\u003c\/span\u003e\u003c\/b\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan lang=\"en-in\"\u003e \u003c\/span\u003e\u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cb\u003eTheory                                                                                          (60 Hours)\u003c\/b\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan\u003e \u003c\/span\u003e\u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cb\u003e\u003cspan\u003eUnit-1                                                                                                                                  (12 hours)\u003c\/span\u003e\u003c\/b\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cb\u003e\u003cspan\u003eGreen Chemistry:\u003c\/span\u003e\u003c\/b\u003e\u003cspan\u003e   \u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan\u003ea)       \u003c\/span\u003e\u003cspan\u003eIntroduction, principles of green chemistry.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan\u003eb)       \u003c\/span\u003e\u003cb\u003e\u003cspan\u003eMicrowave Assisted Reactions:\u003c\/span\u003e\u003c\/b\u003e\u003cspan\u003e Merit and demerits of its use, increased reaction rates, mechanism, superheating effects of microwave, effects of solvents in microwave assisted synthesis, microwave technology in process optimization, its applications in various organic reactions and heterocycles synthesis.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan\u003ec)       \u003c\/span\u003e\u003cb\u003e\u003cspan\u003eUltrasound Assisted Reactions:\u003c\/span\u003e\u003c\/b\u003e\u003cspan\u003e Types of sonochemical reactions, homogenous, heterogeneous liquid-liquid and liquid-solid reactions, synthetic applications\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan\u003ed)       \u003c\/span\u003e\u003cb\u003e\u003cspan\u003eContinuous Flow Reactors:\u003c\/span\u003e\u003c\/b\u003e\u003cspan\u003e Working principle, advantages and synthetic applications.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan\u003e \u003c\/span\u003e\u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan\u003e \u003c\/span\u003e\u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cb\u003e\u003cspan\u003eUnit-2                                                                                                                                 (12 hours)\u003c\/span\u003e\u003c\/b\u003e\u003cspan\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cb\u003e\u003cspan\u003eChemistry of Peptides:\u003c\/span\u003e\u003c\/b\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan\u003ea)       \u003c\/span\u003e\u003cspan\u003eCoupling reactions in peptide synthesis.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan\u003eb)       \u003c\/span\u003e\u003cb\u003e\u003cspan\u003ePrinciples of Solid Phase Peptide Synthesis, T-BOC and FMOC Protocols, various Solid Supports and Linkers:\u003c\/span\u003e\u003c\/b\u003e\u003cspan\u003e Activation procedures, peptide bond formation, deprotection and cleavage from resin, low and high HF cleavage protocols, formation of free peptides and peptide amides, purification and case studies, site-specific chemical modifications of peptides.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan\u003ec)       \u003c\/span\u003e\u003cspan\u003eSegment and sequential strategies for solution phase peptide synthesis with any two case studies.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan\u003ed)       \u003c\/span\u003e\u003cb\u003e\u003cspan\u003eSide Reactions in Peptide Synthesis:\u003c\/span\u003e\u003c\/b\u003e\u003cspan\u003e Deletion peptides, side reactions initiated by proton abstraction, protonation, over activation and side reactions of individual amino acids.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan\u003e \u003c\/span\u003e\u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cb\u003e\u003cspan\u003eUnit-3                                                                                                                                 (12 hours)\u003c\/span\u003e\u003c\/b\u003e\u003cspan\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cb\u003e\u003cspan\u003ePhotochemical Reactions:\u003c\/span\u003e\u003c\/b\u003e\u003cspan\u003e Basic principles of photochemical reactions. Photo-oxidation, photo-addition and photo-fragmentation.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan\u003e \u003c\/span\u003e\u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cb\u003e\u003cspan\u003ePericyclic Reactions: \u003c\/span\u003e\u003c\/b\u003e\u003cspan\u003eMechanism, Types of pericyclic reactions such as cyclo addition, electrocyclic reaction and sigmatrophic rearrangement reactions with examples\u003cb\u003e:\u003c\/b\u003e\u003c\/span\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e \u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cb\u003e\u003cspan\u003eUnit-4                                                                                                                                 (12 hours)\u003c\/span\u003e\u003c\/b\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cb\u003e\u003cspan\u003eCatalysis:\u003c\/span\u003e\u003c\/b\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan\u003ea)       \u003c\/span\u003e\u003cspan\u003eTypes of catalysis, heterogeneous and homogenous catalysis, advantages and disadvantages.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan\u003eb)       \u003c\/span\u003e\u003cb\u003e\u003cspan\u003eHeterogeneous Catalysis:\u003c\/span\u003e\u003c\/b\u003e\u003cspan\u003e Preparation, characterization, kinetics, supported catalysts, catalyst deactivation and regeneration, some examples of heterogeneous catalysis used in synthesis of drugs.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan\u003ec)       \u003c\/span\u003e\u003cspan\u003eHomogenous catalysis, hydrogenation, hydroformylation, hydrocyanation, Wilkinson catalysts, chiral ligands and chiral induction, Ziegler‐Natta catalysts, some examples of homogenous catalysis used in synthesis of drugs.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan\u003ed)       \u003c\/span\u003e\u003cb\u003e\u003cspan\u003eTransition-Metal and Organo-catalysis in Organic Synthesis: \u003c\/span\u003e\u003c\/b\u003e\u003cspan\u003eMetal-catalyzed reactions.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan\u003ee)       \u003c\/span\u003e\u003cb\u003e\u003cspan\u003eBiocatalysis:\u003c\/span\u003e\u003c\/b\u003e\u003cspan\u003e Use of enzymes in organic synthesis, immobilized enzymes\/cells in organic reaction.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan\u003ef)        \u003c\/span\u003e\u003cb\u003e\u003cspan\u003ePhase Transfer Catalysis:\u003c\/span\u003e\u003c\/b\u003e\u003cspan\u003e Theory and applications.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan\u003e \u003c\/span\u003e\u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cb\u003e\u003cspan\u003eUnit-5                                                                                                                                  (12 hours)\u003c\/span\u003e\u003c\/b\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cb\u003e\u003cspan\u003eStereochemistry \u0026amp; Asymmetric Synthesis: \u003c\/span\u003e\u003c\/b\u003e\u003cspan\u003e \u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan\u003ea)       \u003c\/span\u003e\u003cb\u003e\u003cspan\u003eBasic Concepts in Stereochemistry:\u003c\/span\u003e\u003c\/b\u003e\u003cspan\u003e optical activity, specific rotation, racemates and resolution of \u003c\/span\u003e\u003cspan\u003eracemates, the Cahn, Ingold, Prelog (CIP) sequence rule, meso compounds, pseudo asymmetric centres, axes of symmetry, Fischers D and L notation, cis-trans isomerism, E and Z notation.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"MsoNormal\"\u003e\u003cspan\u003eb)       \u003c\/span\u003e\u003cspan\u003eMethods of asymmetric synthesis using chiral pool, chiral auxiliaries and catalytic asymmetric synthesis, enantiopure separation and Stereo selective synthesis with examples. \u003c\/span\u003e\u003c\/p\u003e","brand":"New Vidyasagar Book Mart","offers":[{"title":"Default Title","offer_id":53438070423849,"sku":null,"price":300.0,"currency_code":"INR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0867\/4367\/9273\/files\/Screenshot2026-05-28131640.png?v=1787154919","url":"https:\/\/www.onetouchbook.com\/products\/advanced-organic-chemistry-ii-pharmaceutical-chemistry-m-pharm-second-semester-authors-dr-p-sivakumar-prof-dr-m-sivagamy-dr-m-senthilraja-thakur-publications-pvt-ltd","provider":"OneTouch Book","version":"1.0","type":"link"}