Comprehensive Chirality. Vol.2 : Synthetic methods I – Chiral pool and diastereoselective methods / Erick M. Carreira

Public ISBD Titre de série : Comprehensive Chirality Titre : Vol.2 : Synthetic methods I – Chiral pool and diastereoselective methods Type de document : texte imprimé Auteurs : Erick M. Carreira, Éditeur scientifique ; Hisashi Yamamoto, Éditeur scientifique ; Johann H. Mulzer, Éditeur scientifique Editeur : Amsterdam : Elsevier Année de publication : 2012 Collection : Comprehensive Chirality Importance : xxiii, 782 p. Format : 28 cm ISBN/ISSN/EAN : 978-0-08-095167-6 Langues : Anglais (eng) Note de contenu : "* Introductory remarks: Chiral pool syntheses and diastereoselective reactions * General principles of diastereoselective reactions: Rigid templates * General principles of diastereoselective reactions: Diastereoselectivity via substrate-directable reactions (internal delivery) and heterocyclizations * General principles of diastereoselective reactions: Acyclic control of diastereoselectivity * General principles of diastereoselective reactions: Diastereoselective domino reactions * Chiral pool synthesis: From ?-amino acids and derivatives * Chiral pool synthesis: Starting from terpenes * Chiral pool synthesis: Chiral pool syntheses starting from carbohydrates * Chiral pool synthesis: Chiral pool syntheses from cis-cyclohexadiene diols * Chiral pool synthesis: Chiral pool synthesis from hydroxy acids: Lactic acid, tartaric acid, malic acid, and 2-methyl-3-hydroxypropionic acid * Chiral pool synthesis: Chiral pool synthesis from quinic acid * Selected diastereoselective reactions: Additions of achiral carbanions to chiral aldehydes and ketones * Selected diastereoselective reactions: Aldoltype additions * Selected diastereoselective reactions: Enolate alkylation * Selected diastereoselective reactions: Substrate controlled stereoselective conjugate addition reactions with organocopper reagents * Selected diastereoselective reactions: Free radical additions and cyclizations * Selected diastereoselective reactions: Intramolecular diels–alder reactions * Selected diastereoselective reactions: diastereoselective intra- and intermolecular 1,3-dipolar cycloadditions in natural product synthesis * Selected diastereoselective reactions: Electrocyclizations * Selected diastereoselective reactions: Ionic and zwitterionic cyclizations * Selected diastereoselective reactions: Diastereoface-differentiating claisen, cope, and [2,3]-wittig rearrangements in contemporary natural product synthesis * Selected diastereoselective reactions: Heck type cyclizations * Selected diastereoselective reactions: Gold catalyzed cyclizations * Selected diastereoselective reactions: C–H insertions." Cote : EXCLU (SdL) Num_Inv : 3291 Comprehensive Chirality. Vol.2 : Synthetic methods I – Chiral pool and diastereoselective methods [texte imprimé] / Erick M. Carreira, Éditeur scientifique ; Hisashi Yamamoto, Éditeur scientifique ; Johann H. Mulzer, Éditeur scientifique . - Amsterdam : Elsevier, 2012 . - xxiii, 782 p. ; 28 cm. - (Comprehensive Chirality) . ISBN : 978-0-08-095167-6 Langues : Anglais (eng) Note de contenu : "* Introductory remarks: Chiral pool syntheses and diastereoselective reactions * General principles of diastereoselective reactions: Rigid templates * General principles of diastereoselective reactions: Diastereoselectivity via substrate-directable reactions (internal delivery) and heterocyclizations * General principles of diastereoselective reactions: Acyclic control of diastereoselectivity * General principles of diastereoselective reactions: Diastereoselective domino reactions * Chiral pool synthesis: From ?-amino acids and derivatives * Chiral pool synthesis: Starting from terpenes * Chiral pool synthesis: Chiral pool syntheses starting from carbohydrates * Chiral pool synthesis: Chiral pool syntheses from cis-cyclohexadiene diols * Chiral pool synthesis: Chiral pool synthesis from hydroxy acids: Lactic acid, tartaric acid, malic acid, and 2-methyl-3-hydroxypropionic acid * Chiral pool synthesis: Chiral pool synthesis from quinic acid * Selected diastereoselective reactions: Additions of achiral carbanions to chiral aldehydes and ketones * Selected diastereoselective reactions: Aldoltype additions * Selected diastereoselective reactions: Enolate alkylation * Selected diastereoselective reactions: Substrate controlled stereoselective conjugate addition reactions with organocopper reagents * Selected diastereoselective reactions: Free radical additions and cyclizations * Selected diastereoselective reactions: Intramolecular diels–alder reactions * Selected diastereoselective reactions: diastereoselective intra- and intermolecular 1,3-dipolar cycloadditions in natural product synthesis * Selected diastereoselective reactions: Electrocyclizations * Selected diastereoselective reactions: Ionic and zwitterionic cyclizations * Selected diastereoselective reactions: Diastereoface-differentiating claisen, cope, and [2,3]-wittig rearrangements in contemporary natural product synthesis * Selected diastereoselective reactions: Heck type cyclizations * Selected diastereoselective reactions: Gold catalyzed cyclizations * Selected diastereoselective reactions: C–H insertions." Cote : EXCLU (SdL) Num_Inv : 3291

Exemplaires(1)

Code-barres	Cote	Support	Localisation	Section	Disponibilité
3291	EXCLU	Texte imprimé	Salle de lecture	Encyclopédie	Consultation sur place Exclu du prêt

Topics in Current Chemistry. Vol.243 : Natural product synthesis I: Targets, methods, concepts / Johann H. Mulzer

Public ISBD Titre de série : Topics in Current Chemistry Titre : Vol.243 : Natural product synthesis I: Targets, methods, concepts Type de document : texte imprimé Auteurs : Johann H. Mulzer, Éditeur scientifique Editeur : Berlin, Heidelberg : Springer Année de publication : 2005 Collection : Topics in Current Chemistry, ISSN 0340-1022 num. 243 Importance : x, 239 p. Format : 24 cm ISBN/ISSN/EAN : 978-3-540-21125-9 Langues : Anglais (eng) Note de contenu : "* Total synthesis of kalsoene and preussin * Paraconic acids- the natural products from lichen symbiont * Recent progress in the total synthesis of dolabellane and dolastane diterpenes * Strategies for total and diversity-oriented synthesis of natural product (-Like) macrolides * Enantioselective synthesis of C(8)-hydroxylated lignans: Early approaches and recent advances." Cote : EXCLU (SdL) Num_Inv : 2704 Topics in Current Chemistry. Vol.243 : Natural product synthesis I: Targets, methods, concepts [texte imprimé] / Johann H. Mulzer, Éditeur scientifique . - Berlin, Heidelberg : Springer, 2005 . - x, 239 p. ; 24 cm. - (Topics in Current Chemistry, ISSN 0340-1022; 243) . ISBN : 978-3-540-21125-9 Langues : Anglais (eng) Note de contenu : "* Total synthesis of kalsoene and preussin * Paraconic acids- the natural products from lichen symbiont * Recent progress in the total synthesis of dolabellane and dolastane diterpenes * Strategies for total and diversity-oriented synthesis of natural product (-Like) macrolides * Enantioselective synthesis of C(8)-hydroxylated lignans: Early approaches and recent advances." Cote : EXCLU (SdL) Num_Inv : 2704

Exemplaires(1)

Code-barres	Cote	Support	Localisation	Section	Disponibilité
2704	EXCLU	Texte imprimé	Salle de lecture	Série	Consultation sur place Exclu du prêt

Topics in Current Chemistry. Vol.244 : Natural product synthesis II: Targets, methods, concepts / Johann H. Mulzer

Public ISBD Titre de série : Topics in Current Chemistry Titre : Vol.244 : Natural product synthesis II: Targets, methods, concepts Type de document : texte imprimé Auteurs : Johann H. Mulzer, Éditeur scientifique Editeur : Berlin, Heidelberg : Springer Année de publication : 2005 Collection : Topics in Current Chemistry, ISSN 0340-1022 num. 244 Importance : x, 270 p. Format : 24 cm ISBN/ISSN/EAN : 978-3-540-21124-2 Langues : Anglais (eng) Note de contenu : "* Marine natural products from Pseudopterogorgia elisabethae: Structures, biosynthesis, pharmacology and total synthesis * Vinylogous aldol reactions and their applications in the syntheses of natural products * Methanophenazine and other natural biologically active phenazines * Occurrence, biological activity, and convergent organometallic synthesis of carbazole alkaloids * Charge accelerated aza-claisen rearrangements * Synthetic studies on the pamamycin macrodiolides." Cote : EXCLU (SdL) Num_Inv : 2722 Topics in Current Chemistry. Vol.244 : Natural product synthesis II: Targets, methods, concepts [texte imprimé] / Johann H. Mulzer, Éditeur scientifique . - Berlin, Heidelberg : Springer, 2005 . - x, 270 p. ; 24 cm. - (Topics in Current Chemistry, ISSN 0340-1022; 244) . ISBN : 978-3-540-21124-2 Langues : Anglais (eng) Note de contenu : "* Marine natural products from Pseudopterogorgia elisabethae: Structures, biosynthesis, pharmacology and total synthesis * Vinylogous aldol reactions and their applications in the syntheses of natural products * Methanophenazine and other natural biologically active phenazines * Occurrence, biological activity, and convergent organometallic synthesis of carbazole alkaloids * Charge accelerated aza-claisen rearrangements * Synthetic studies on the pamamycin macrodiolides." Cote : EXCLU (SdL) Num_Inv : 2722

Exemplaires(1)

Code-barres	Cote	Support	Localisation	Section	Disponibilité
2722	EXCLU	Texte imprimé	Salle de lecture	Série	Consultation sur place Exclu du prêt

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