00750nam2-2200289---450 99000082440020331620230116102651.02-7283-0009-90082440USA010082440(ALEPH)000082440USA01008244020011221f1992----|||||ita|01 bafreIT|||| |||||Planches2RomaÉcole française de Rome1992XII, 429 p.tavole31 cm00100824342001<<Le>> Palais FarneseITsalbcISBD990000824400203316XII.2.B. 176/2(VII A 137 2)96538 L.M.VII ABKUMAPlanches929252UNISA01086nam0-22003491i-450 99000324132040332120230421144026.088-7104-214-X000324132FED01000324132(Aleph)000324132FED0100032413220030910d1990----km-y0itay50------baitaITy-------001yyAspetti metodologici della programmazione regionale nel piano di sviluppo del MolisePier Luigi AmorosoNapoliEdizioni Scientifiche Italiane1990105 p.24 cmPubblicazioni dell'Università degli studi del Molise. Sez. Monografie, studi economici1MoliseProgrammazione economica338.945719Amoroso,Pier Luigi361318ITUNINARICAUNIMARCBK990003241320403321050.002.AMO1529DECGEO1-O2.13810299DECTSDECGEDECTSASPETTI METODOLOGICI449000UNINA05433nam 22006734a 450 991102020990332120200520144314.09786610197040978128019704812801970489780470988619047098861497814051447971405144793(CKB)1000000000341892(EBL)233026(OCoLC)475939152(SSID)ssj0000254830(PQKBManifestationID)11213137(PQKBTitleCode)TC0000254830(PQKBWorkID)10213123(PQKB)11234658(MiAaPQ)EBC233026(Perlego)2776858(EXLCZ)99100000000034189220040809d2005 uy 0engur|n|---|||||txtccrSynthesis of naturally occurring nitrogen heterocycles from carbohydrates /El Sayed H. El Ashry, Ahmed El NemrOxford, UK ;Ames, Iowa Blackwell Pub.20051 online resource (466 p.)Description based upon print version of record.9781405129343 1405129344 Includes bibliographical references and indexes.Synthesis of Naturally Occurring Nitrogen Heterocycles from Carbohydrates; Contents; Preface; Author details; List of abbreviations and acronyms used in this book; Introduction; 1. Five-membered nitrogen heterocycles; 1.1 Hydroxymethylpyrrolidines; 1.1.1 2-Hydroxymethylpyrrolidines; 1.1.1.1 Synthesis from D-glucose; 1.1.1.2 Synthesis from D-mannose; 1.1.1.3 Synthesis from L-arabinose; 1.1.1.4 Synthesis from D-xylose; 1.1.1.5 Synthesis from D-threose; 1.1.1.6 Synthesis from D-lyxonolactone; 1.1.1.7 Synthesis from D-gulonolactone; 1.1.2 Dihydro-2-hydroxymethylpyrrole (nectrisine)1.1.2.1 Synthesis from D-glucose1.1.2.2 Synthesis from D-arabinose; 1.1.2.3 Synthesis from D-glyceraldehyde; 1.1.2.4 Synthesis from L-threitol; 1.1.3 2,5-Dihydroxymethylpyrrolidines; 1.1.3.1 Synthesis from D-glucose; 1.1.3.2 Synthesis from D-glucosamine; 1.1.3.3 Synthesis from D-fructose; 1.1.3.4 Synthesis from L-sorbose; 1.1.3.5 Synthesis from D-arabinose; 1.1.3.6 Synthesis from L-xylose; 1.1.3.7 Synthesis from D-iditol; 1.1.3.8 Synthesis from D-mannitol; 1.1.3.9 Synthesis from D-glucosamic acid; 1.1.3.10 Synthesis from D-glyconolactone; 1.2 2-Carboxypyrrolidines; 1.2.1 Hydroxyprolines1.2.1.1 Synthesis from D-glucose1.2.1.2 Synthesis from D-mannitol; 1.2.1.3 Synthesis from L-arabinono- and L-lyxono-lactones; 1.2.1.4 Synthesis from D-ribonolactone; 1.2.1.5 Synthesis from D-gulonolactones; 1.2.1.6 Synthesis from D-gluconolactone; 1.2.1.7 Synthesis from D-glucoronolactone; 1.2.1.8 Synthesis from D-xylonolactone; 1.2.2 Bulgecins; 1.2.2.1 Synthesis from D-glucose; 1.2.2.2 Synthesis from D-glucuronolactone; 1.3 2-Aralkyl pyrrolidines; 1.3.1 (-)-Anisomycin; 1.3.1.1 Synthesis from D-galactose; 1.3.1.2 Synthesis from L-arabinose; 1.3.1.3 Synthesis from D-ribose1.3.1.4 Synthesis from L-threose1.3.1.5 Synthesis from L-threitol; 1.3.1.6 Synthesis from D-mannitol; 1.3.2 (+)-Preussin; 1.3.2.1 Synthesis from D-glucose; 1.3.2.2 Synthesis from D-mannose; 1.3.2.3 Synthesis from D-arabinose; 1.4 2-Aryl pyrrolidines; 1.4.1 Codonopsinine and codonopsine; 1.5 Miscellaneous; 1.5.1 Detoxins; 1.5.1.1 Synthesis from D-glucose; 1.5.1.2 Synthesis from L-ascorbic acid; 1.5.2 Gualamycin; 1.5.3 Lactacystin; 2. Five-membered heterocycles with two heteroatoms; 2.1 (+)-Hydantocidin; 2.1.1 Synthesis from D-fructose; 2.1.2 Synthesis from D-ribose2.1.3 Synthesis from D-threose2.1.4 Synthesis from D-ribonolactone; 2.2 Bleomycin; 2.2.1 Synthesis from D-glucosamine; 2.2.2 Synthesis from L-rhamnose; 2.2.3 Total synthesis of bleomycin A2; 2.3 Calyculins; 2.3.1 Synthesis from D-lyxose; 2.3.2 Synthesis from D-gulonolactone; 2.3.3 Synthesis from L-idonolactone; 2.3.4 Synthesis from D-ribonolactone; 2.3.5 Synthesis from D-erythronolactone; 2.4 Acivicin; 2.5 Bengazole; 3. Six-membered nitrogen heterocycles; 3.1 Hydroxymethylpiperidines; 3.1.1 Nojirimycin; 3.1.1.1 Synthesis from D-glucose; 3.1.1.2 Synthesis from L-sorbose3.1.1.3 Synthesis from L-threoseCarbohydrates are widely distributed in nature and widely available, and so are considered as a promising feedstock for the preparation of many organic chemical compounds. They are particularly useful in the preparation of nitrogen heterocycles because of their related structural characteristics and easy availability. Synthesis of Naturally Occurring Nitrogen Heterocycles from Carbohydrates will review the recent literature dealing with use of carbohydrates as raw materials in the synthesis of these materials. The text contains six chapters arranged according to the compleHeterocyclic compoundsSynthesisCarbohydratesHeterocyclic compoundsSynthesis.Carbohydrates.547/.590459El Ashry El Sayed H.1942-969036El-Nemr Ahmed1962-936000MiAaPQMiAaPQMiAaPQBOOK9911020209903321Synthesis of naturally occurring nitrogen heterocycles from carbohydrates2201514UNINA