01548nam--2200445---450-99000058328020331620101210121940.088-217-0888-80058328USA010058328(ALEPH)000058328USA01005832820010724d1996----km-y0itay0103----baitaIT||||||||001yyGuida al nuovo processo tributariocommentario al D.Lgs. n.546/1992 con formularioaggiornato con C.M. 98/E del 23 aprile 1996 e D.L. 16 maggio 1996, n.259Oliviero Drigani, Roberto Lunellipresentazione di Augusto FantozziMilanofiore, AssagoIPSOA1996XIII, 477 p.24 cmNuove leggi & commenti2001Nuove leggi & commentiProcesso tributarioContenzioso tributario343.45040269DRIGANI,Oliviero546944LUNELLI,Roberto414299FANTOZZI,AugustoITsalbcISBD990000583280203316XXIV.5.C. 593 (IG VII 446)13467 GXXIV.5.C. 593 (IG VII)00250078BKGIUPATTY9020010724USA011557PATTY9020010724USA01155820020403USA011707PATRY9020040406USA011640RSIAV39020090901USA011357RSIAV29020101210USA011219Guida al nuovo processo tributario883726UNISA05363nam 22006374a 450 99620534820331620230617005256.01-280-19704-897866101970400-470-98861-41-4051-4479-3(CKB)1000000000341892(EBL)233026(OCoLC)475939152(SSID)ssj0000254830(PQKBManifestationID)11213137(PQKBTitleCode)TC0000254830(PQKBWorkID)10213123(PQKB)11234658(MiAaPQ)EBC233026(EXLCZ)99100000000034189220040809d2005 uy 0engur|n|---|||||txtccrSynthesis of naturally occurring nitrogen heterocycles from carbohydrates[electronic resource] /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.1-4051-2934-4 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.547.593547/.590459572.54El Ashry El Sayed H.1942-969036El-Nemr Ahmed1962-936000MiAaPQMiAaPQMiAaPQBOOK996205348203316Synthesis of naturally occurring nitrogen heterocycles from carbohydrates2201514UNISA