Nantilus
Heterocycles from Carbohydrate Precursors
This book is a volume in the series Topics in Heterocyclic Chemistry.Itc- ers the key methods used for designing synthetic approaches to heterocycles from carbohydrates and the value and scope of these methods. Carbohydrates are widely distributed in nature and constitute the largest part of renewab...
Enregistré dans:
| Auteur principal : | |
|---|---|
| Autres auteurs : | |
| Format : | Livre |
| Langue : | anglais |
| Titre complet : | Heterocycles from Carbohydrate Precursors / edited by El Sayed H. El Ashry. |
| Publié : |
Berlin, Heidelberg :
Springer Berlin Heidelberg
, [20..] Cham : Springer e-books Springer Nature |
| Collection : | Topics in heterocyclic chemistry (Print) ; 7 |
| Titre de l'ensemble : | Topics in Heterocyclic Chemistry vol. 7 |
| 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 : | Manipulation of Carbohydrate Carbon Atoms for the Synthesis of Heterocycles. Synthesis of Heterocycles from Glycosylamines and Glycosyl Azides. Heterocycles from Carbohydrate Isothiocyanates. ?-Lactams from Carbohydrates. Azide Alkyne 1,3-Dipolar Cycloadditions: a Valuable Tool in Carbohydrate Chemistry. Synthesis of Glycoporphyrins. New Developments in the Synthesis of Anisomycin and Its Analogues. 1,3-Dipolar Cycloadditions of Sugar-Derived Nitrones and their Utilization in Synthesis. Anhydro Sugars: Useful Tools for Chiral Syntheses of Heterocycles |
| Sujets : | |
| Documents associés : | Autre format:
Heterocycles from carbohydrate precursors |
| LEADER | 04857clm a2200625 4500 | ||
|---|---|---|---|
| 001 | PPN123162866 | ||
| 003 | http://www.sudoc.fr/123162866 | ||
| 005 | 20241002160300.0 | ||
| 010 | |a 978-3-540-72957-0 | ||
| 017 | 7 | 0 | |a 10.1007/978-3-540-72957-0 |2 DOI |
| 035 | |a (OCoLC)647108202 | ||
| 035 | |a Springer978-3-540-72957-0 | ||
| 035 | |a Springer-11644-978-3-540-72957-0 | ||
| 035 | |a SPRINGER_EBOOKS_LN_PLURI_10.1007/978-3-540-72957-0 | ||
| 100 | |a 20080410f20 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 Heterocycles from Carbohydrate Precursors |f edited by El Sayed H. El Ashry. | |
| 214 | 0 | |a Berlin, Heidelberg |c Springer Berlin Heidelberg |c Springer e-books | |
| 214 | 2 | |a Cham |c Springer Nature |d [20..] | |
| 225 | 1 | |a Topics in Heterocyclic Chemistry |x 1861-9282 |v 7 | |
| 327 | 1 | |a Manipulation of Carbohydrate Carbon Atoms for the Synthesis of Heterocycles |a Synthesis of Heterocycles from Glycosylamines and Glycosyl Azides |a Heterocycles from Carbohydrate Isothiocyanates |a ?-Lactams from Carbohydrates |a Azide Alkyne 1,3-Dipolar Cycloadditions: a Valuable Tool in Carbohydrate Chemistry |a Synthesis of Glycoporphyrins |a New Developments in the Synthesis of Anisomycin and Its Analogues |a 1,3-Dipolar Cycloadditions of Sugar-Derived Nitrones and their Utilization in Synthesis |a Anhydro Sugars: Useful Tools for Chiral Syntheses of Heterocycles | |
| 330 | |a This book is a volume in the series Topics in Heterocyclic Chemistry.Itc- ers the key methods used for designing synthetic approaches to heterocycles from carbohydrates and the value and scope of these methods. Carbohydrates are widely distributed in nature and constitute the largest part of renewable biomasses. Moreover, many carbohydrates and their derivatives are comm- cially available at relatively cheap prices. Consequently their utilization is highly encouraged and economically they are of great signi?cance. Moreover, carbohydrates are highly functionalized compounds that can be readily deri- tized and/or cyclized to provide heterocyclic compounds. This book provides a modern account and an up-to-date description of the advancement in the synthesis of diverse heterocycles from carbohydrates. Carbohydrates can be considered as a source of chiral centers in addition to the variable modi?cation thereof. Herein the elaboration of the carbohydrate molecules for providing different heterocycles is the main objective and team efforts from leaders of the topics has been gathered in this volume. This book is designed to be suitable for students and researchers. It is highly recommended as a reference book and for teaching the fascinating topics related to carbohydrates, heterocycles and organic synthesis. In addition to its importance in academia, it is also an excellent source for information about the variety of methods used in the synthesis of heterocycles important to industry | ||
| 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 7 | |
| 452 | | | |0 128522011 |t Heterocycles from carbohydrate precursors |f Volume Editor : El Sayed H. El Ashry |c Berlin |n Springer |d 2007 |p 1 vol. (X- 354 p.) |s Topics in heterocyclic chemistry |y 978-3-540-72956-3 | |
| 517 | | | |a With contributions by numerous experts | |
| 610 | 1 | |a Chemistry | |
| 610 | 2 | |a Organic Chemistry | |
| 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 | ||
| 676 | |a 547 |v 23 | ||
| 680 | |a QD415-436 | ||
| 700 | 1 | |a El Ashry |b El Sayed H. |4 070 | |
| 702 | 1 | |a Ashry |b El Sayed H. El |4 340 | |
| 801 | 3 | |a FR |b Abes |c 20231011 |g AFNOR | |
| 801 | 1 | |a DE |b Springer |c 20160105 |g AACR2 | |
| 856 | 4 | |q PDF |u https://doi.org/10.1007/978-3-540-72957-0 |z Accès sur la plateforme de l'éditeur | |
| 856 | 4 | |u https://revue-sommaire.istex.fr/ark:/67375/8Q1-30TZH1G0-C |z Accès sur la plateforme Istex | |
| 856 | 4 | |5 441099901:830931279 |u https://budistant.univ-nantes.fr/login?url=https://doi.org/10.1007/978-3-540-72957-0 | |
| 915 | |5 441099901:830931279 |b SPRING4-00447 | ||
| 930 | |5 441099901:830931279 |b 441099901 |j g | ||
| 979 | |a NUM | ||
| 991 | |5 441099901:830931279 |a Exemplaire créé en masse par ITEM le 01-10-2024 15:47 | ||
| 997 | |a NUM |b SPRING4-00447 |d NUMpivo |e EM |s d | ||
| 998 | |a 980384 | ||