LEADER 03329oam 2200637zu 450 001 9911020359103321 005 20230421042412.0 010 $a1-280-55850-4 010 $a9786610558506 010 $a3-527-60083-3 035 $a(CKB)1000000000019217 035 $a(SSID)ssj0000289567 035 $a(PQKBManifestationID)11221486 035 $a(PQKBTitleCode)TC0000289567 035 $a(PQKBWorkID)10385530 035 $a(PQKB)11341298 035 $a(MiAaPQ)EBC4957763 035 $a(Au-PeEL)EBL4957763 035 $a(CaONFJC)MIL55850 035 $a(OCoLC)85820525 035 $a(NjHacI)991000000000019217 035 $a(EXLCZ)991000000000019217 100 $a20160829d1998 uy 101 0 $aeng 135 $aurcnu|||||||| 181 $ctxt 182 $cc 183 $acr 200 10$aAzolides in Organic Synthesis and Biochemistry 210 31$a[Place of publication not identified]$cWiley VCH Imprint$d1998 215 $a1 online resource (503 pages) 300 $aBibliographic Level Mode of Issuance: Monograph 311 $a3-527-29314-0 327 $aReactivity of azolides -- Preparation and properties of azolides -- Syntheses of carboxylic and carbonic esters -- Syntheses of amides and analogous compounds with CO-NR functions -- Synthesis of peptides -- Modification and immobilization of proteins (enzymes) -- Syntheses of heterocycles -- Synthesis of isocyanates, isothiocyanates, aminoisocyanates, aminoisothiocyanates, and N-sulfinylamines -- Reactions of imino analogues of azolides -- Syntheses of sulfonates, sulfinates, sulfonamides, sulfoxylates, sulfones, sulfoxides, sulfites, sulfates, and sulfanes -- Reaction of phosphines with N, N1-carbonyldiimidazole (CDI) -- Phosphorylation and nucleotide-syntheses -- Syntheses of acid anhydrides and acyl chlorides -- C-Acylations by azolides -- Reduction of azolides to aldehydes and alcohols -- Deoxygenation of alcohols and C-C coupling reactions -- Synthesis of glycosides and ethers -- Dehydration reactions -- Substitution reactions on azoles -- Azoic-transfer reactions to carbon atoms -- Syntheses of organic halides/pseudohalides and aromatic amines -- Reactions of vinylogous azolides -- Photochemical reactions -- Azolides in medicinal and industrial fields and in analytical methods. 330 $aPreparation, properties and the manifold synthetic applications of "azolides" in organic syntheses are the topics of this book. Since the first review in "Angewandte Chemie" in 1962, shortly after the discovery of this class of compounds by H. Staab, they became widely used in different fields of organic chemistry. 606 $aAmides 606 $aAzo compounds 606 $aHeterocyclic compounds$xSynthesis 606 $aChemistry, Organic 606 $aOrganic compounds$xSynthesis 606 $aPyrroles 615 0$aAmides. 615 0$aAzo compounds. 615 0$aHeterocyclic compounds$xSynthesis. 615 0$aChemistry, Organic. 615 0$aOrganic compounds$xSynthesis. 615 0$aPyrroles. 676 $a547.0430459 700 $aStaab$b Heinz A$01841749 702 $aSchneider$b K. M 702 $aBauer$b H 801 0$bPQKB 906 $aBOOK 912 $a9911020359103321 996 $aAzolides in Organic Synthesis and Biochemistry$94421584 997 $aUNINA