Bioactive Heterocycles II

As part of the series Topics in Heterocyclic Chemistry,this volume titled Bio- tive Heterocycles II presents comprehensive and up-to-date reviews on selected topics regarding synthetic as well as naturally occurring bioactive heterocycles. The ?rst chapter, High Pressure Synthesis of Heterocycles Re...

Description complète

Enregistré dans:
Détails bibliographiques
Auteur principal : Eguchi Shoji (Éditeur scientifique)
Format : Livre
Langue : anglais
Titre complet : Bioactive Heterocycles II / edited by Shoji Eguchi.
Publié : Berlin, Heidelberg : Springer Berlin Heidelberg , [20..]
Cham : Imprint: Springer
Springer Nature
Collection : Topics in heterocyclic chemistry (Print) ; 8
Titre de l'ensemble : Topics in Heterocyclic Chemistry vol. 8
Accès en ligne : Accès Nantes Université
Accès direct soit depuis les campus via le réseau ou le wifi eduroam soit à distance avec un compte @etu.univ-nantes.fr ou @univ-nantes.fr
Note sur l'URL : Accès sur la plateforme de l'éditeur
Accès sur la plateforme Istex
Condition d'utilisation et de reproduction : Conditions particulières de réutilisation pour les bénéficiaires des licences nationales : https://www.licencesnationales.fr/springer-nature-ebooks-contrat-licence-ln-2017
Contenu : High-Pressure Synthesis of Heterocycles Related to Bioactive Molecules. Ring Transformation of Nitropyrimidinone Leading to Versatile Azaheterocyclic Compounds. Synthesis of Thalidomide. Rational Drug Design of ? Opioid Receptor Agonist TAN-67 from ? Opioid Receptor Antagonist NTI. Tetrahydrobiopterin and Related Biologically Important Pterins. Preparation, Structure, and Biological Properties of Phosphorus Heterocycles with a C? ?P Ring System. The Role of the Membrane Actions of Phenothiazines and Flavonoids as Functional Modulators
Sujets :
Documents associés : Autre format: Bioactive heterocycles II
LEADER 05071clm a2200649 4500
001 PPN123727626
003 http://www.sudoc.fr/123727626
005 20241002160300.0
010 |a 978-3-540-72592-3 
017 7 0 |a 10.1007/978-3-540-72592-3  |2 DOI 
035 |a (OCoLC)647109368 
035 |a Springer978-3-540-72592-3 
035 |a Springer-11644-978-3-540-72592-3 
035 |a SPRINGER_EBOOKS_LN_PLURI_10.1007/978-3-540-72592-3 
100 |a 20080505f20 u y0frey0103 ba 
101 0 |a eng  |2 639-2 
102 |a DE 
135 |a dr||||||||||| 
181 |6 z01  |c txt  |2 rdacontent 
181 1 |6 z01  |a i#  |b xxxe## 
182 |6 z01  |c c  |2 rdamedia 
182 1 |6 z01  |a b 
183 |6 z01  |a ceb  |2 RDAfrCarrier 
200 1 |a Bioactive Heterocycles II  |f edited by Shoji Eguchi. 
214 0 |a Berlin, Heidelberg  |c Springer Berlin Heidelberg  |c Imprint: Springer 
214 2 |a Cham  |c Springer Nature  |d [20..] 
225 1 |a Topics in Heterocyclic Chemistry  |x 1861-9282  |v 8 
327 1 |a High-Pressure Synthesis of Heterocycles Related to Bioactive Molecules  |a Ring Transformation of Nitropyrimidinone Leading to Versatile Azaheterocyclic Compounds  |a Synthesis of Thalidomide  |a Rational Drug Design of ? Opioid Receptor Agonist TAN-67 from ? Opioid Receptor Antagonist NTI  |a Tetrahydrobiopterin and Related Biologically Important Pterins  |a Preparation, Structure, and Biological Properties of Phosphorus Heterocycles with a C? ?P Ring System  |a The Role of the Membrane Actions of Phenothiazines and Flavonoids as Functional Modulators 
330 |a As part of the series Topics in Heterocyclic Chemistry,this volume titled Bio- tive Heterocycles II presents comprehensive and up-to-date reviews on selected topics regarding synthetic as well as naturally occurring bioactive heterocycles. The ?rst chapter, High Pressure Synthesis of Heterocycles Related to Bio- tive Molecules by Kiyoshi Matsumoto, presents a unique high-pressure s- thetic methodology in heterocyclic chemistry. Basic principles and fruitful examples for pericyclic reactions, such as Diels-Alder reactions, 1,3-dipolar reactions, and also for ionic reactions, such as S and addition reactions, are N discussed. The review will be of considerable interest to heterocyclic chemists and synthetic chemists. The second chapter, Ring Transformation of Nitropyrimidinone Leading to Versatile Azaheterocyclic Compounds by Nagatoshi Nishiwaki and Masahiro Ariga, presents a very critical review on novel ring transformations of di- tropyridones and nitropyrimidinones based on the work of his group. - dressed in this review is the synthesis of functionalized molecules, such as nitroanilines, nitropyridines, and nitrophenols, by the ring transformation of dinitropyridones as the nitromalonaldehyde equivalent. Ring transformations of nitropyrimidinones with dinucleophiles to 4-pyridones, pyrimidines and 4-aminopyridines, and to polyfunctinal pyridones with 1,3-dicarbonyl c- pounds, etc., are also discussed. This review may attract the interest of synthetic chemists as well as heterocyclic chemists in the life science ?elds. The third chapter, Synthesis of Thalidomide by Norio Shibata, Takeshi Yamamoto and Takeshi Toru, describes a modern synthetic aspect of thali- mide 
371 0 |a Accès en ligne pour les établissements français bénéficiaires des licences nationales 
371 0 |a Accès soumis à abonnement pour tout autre établissement 
371 1 |a Conditions particulières de réutilisation pour les bénéficiaires des licences nationales  |c https://www.licencesnationales.fr/springer-nature-ebooks-contrat-licence-ln-2017 
410 | |0 113725590  |t Topics in heterocyclic chemistry (Print)  |x 1861-9282  |v 8 
452 | |0 129809705  |t Bioactive heterocycles II  |f Volume Editor : Shoji Eguchi  |c Berlin  |n Springer  |d 2007  |p 1 vol. (X- 309 p.)  |s Topics in heterocyclic chemistry  |y 978-3-540-72591-6 
517 | |a With contributions by numerous experts 
610 1 |a Chemistry 
610 2 |a Organic Chemistry 
610 2 |a Biochemistry, general 
610 2 |a Medicinal Chemistry 
615 |a @Chemistry and Materials Science  |n 11644; ZDB-2-CMS  |2 Springer 
615 |a @Chemistry and Materials Science  |n 11644  |2 Springer 
615 |a Chemistry and Materials Science  |n 11644  |2 Springer 
676 |a 547  |v 23 
680 |a QD415-436 
700 1 |a Eguchi  |b Shoji  |4 070 
702 1 |a Eguchi  |b Shoji  |4 340 
801 3 |a FR  |b Abes  |c 20240911  |g AFNOR 
801 1 |a DE  |b Springer  |c 20191002  |g AACR2 
856 4 |q PDF  |u https://doi.org/10.1007/978-3-540-72592-3  |z Accès sur la plateforme de l'éditeur 
856 4 |u https://revue-sommaire.istex.fr/ark:/67375/8Q1-3LGPXSMK-2  |z Accès sur la plateforme Istex 
856 4 |5 441099901:830931252  |u https://budistant.univ-nantes.fr/login?url=https://doi.org/10.1007/978-3-540-72592-3 
915 |5 441099901:830931252  |b SPRING4-00445 
930 |5 441099901:830931252  |b 441099901  |j g 
979 |a NUM 
991 |5 441099901:830931252  |a Exemplaire créé en masse par ITEM le 01-10-2024 15:47 
997 |a NUM  |b SPRING4-00445  |d NUMpivo  |e EM  |s d 
998 |a 980423