Organic Syntheses Based on Name Reactions /

By: Hassner, AMaterial type: TextTextPublication details: Elsevier, 2012ISBN: 9780080966304Online resources: Click here to access online
Contents:
ABIKO–MASAMUNE Asymmetric Aldol Reaction to AUWERS–INHOFFEN Dienone-Phenol Rearrangement BAER–FISCHER Amino Sugar Synthesis to BURTON Aromatic Trifluoromethylation CADOGAN Nitroaromatics Cyclization to CURTIUS Acyl Azide Rearrangement DAKIN Phenol Oxidation to DUTT–WORMALL Azide Synthesis EATON Acid Reagent to EVANS Chiral Auxiliary FAVORSKI α-Haloketone Rearrangement to FŰRSTNER Fe Catalyzed CC Coupling GABRIEL–HEINE Aziridine Isomerization to GUY–LEMAIRE–GUETTE Halogenation Reagent HADDADIN–ISSIDORIDES Quinoxaline Synthesis to HUNSDIECKER Halodecarboxylation IRELAND Allyl Ester Rearrangement to IVANOV Carboxy-Grignard Reagent JACOBSEN Asymmetric Epoxidation to JUNG–OLAH–VORONKOV Ether Cleavage KABACHNIK–FIELD Aminophosphonate Synthesis to KURSANOV–PARNES Ionic Hydrogenation LADENBURG Pyridine Benzylation to LUCHE Zn Allylation MACDONALD Porphyrin Synthesis to MYERS–SAITO Cycloaromatization NAGATA Aluminium Cyanide Reagent to NUGENT–RAJANBABU Epoxide Homolysis O'DONNELL Amino Acid Synthesis to Oxy-COPE Hydroxydiene Rearrangement PAAL–KNORR Pyrrole Synthesis to PURDIE Sugar OH Methylation RAMBERG–BACKLUND Olefin Synthesis to RUZICKA–FUKUSHIMA Ketosteroid Rearrangement SAEGUSA Enone Synthesis to SZARVASY–SCHÖPF Carbomethoxylation TAKAI Zn CO Olefination to TSUJI–TROST Allylation UEMURA–DOYLE Rh Allylic Oxidation to URECH Cyanohydrin Synthesis VAN BOOM Phosphorylating Reagent to VORBRÜGGEN Nucleoside Synthesis WACKER–TSUJI Olefin Oxidation to WÜRTZ Coupling YAMADA Peptide Coupling to YONEMITSU 3-Component Condensation ZARD Radical Aminomethylation via Xanthates to ZVILICHOVSKY Heterocycle Synthesis
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ABIKO–MASAMUNE Asymmetric Aldol Reaction to AUWERS–INHOFFEN Dienone-Phenol Rearrangement

BAER–FISCHER Amino Sugar Synthesis to BURTON Aromatic Trifluoromethylation

CADOGAN Nitroaromatics Cyclization to CURTIUS Acyl Azide Rearrangement

DAKIN Phenol Oxidation to DUTT–WORMALL Azide Synthesis

EATON Acid Reagent to EVANS Chiral Auxiliary

FAVORSKI α-Haloketone Rearrangement to FŰRSTNER Fe Catalyzed CC Coupling

GABRIEL–HEINE Aziridine Isomerization to GUY–LEMAIRE–GUETTE Halogenation Reagent

HADDADIN–ISSIDORIDES Quinoxaline Synthesis to HUNSDIECKER Halodecarboxylation

IRELAND Allyl Ester Rearrangement to IVANOV Carboxy-Grignard Reagent

JACOBSEN Asymmetric Epoxidation to JUNG–OLAH–VORONKOV Ether Cleavage

KABACHNIK–FIELD Aminophosphonate Synthesis to KURSANOV–PARNES Ionic Hydrogenation

LADENBURG Pyridine Benzylation to LUCHE Zn Allylation

MACDONALD Porphyrin Synthesis to MYERS–SAITO Cycloaromatization

NAGATA Aluminium Cyanide Reagent to NUGENT–RAJANBABU Epoxide Homolysis

O'DONNELL Amino Acid Synthesis to Oxy-COPE Hydroxydiene Rearrangement

PAAL–KNORR Pyrrole Synthesis to PURDIE Sugar OH Methylation

RAMBERG–BACKLUND Olefin Synthesis to RUZICKA–FUKUSHIMA Ketosteroid Rearrangement

SAEGUSA Enone Synthesis to SZARVASY–SCHÖPF Carbomethoxylation

TAKAI Zn CO Olefination to TSUJI–TROST Allylation

UEMURA–DOYLE Rh Allylic Oxidation to URECH Cyanohydrin Synthesis

VAN BOOM Phosphorylating Reagent to VORBRÜGGEN Nucleoside Synthesis

WACKER–TSUJI Olefin Oxidation to WÜRTZ Coupling

YAMADA Peptide Coupling to YONEMITSU 3-Component Condensation

ZARD Radical Aminomethylation via Xanthates to ZVILICHOVSKY Heterocycle Synthesis


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