LEADER 03281nam 22006015 450 001 9910768162203321 005 20200704175759.0 010 $a3-319-31554-4 024 7 $a10.1007/978-3-319-31554-6 035 $a(CKB)3710000000711718 035 $a(DE-He213)978-3-319-31554-6 035 $a(MiAaPQ)EBC6286261 035 $a(MiAaPQ)EBC5577476 035 $a(Au-PeEL)EBL5577476 035 $a(OCoLC)949921629 035 $a(PPN)194077373 035 $a(EXLCZ)993710000000711718 100 $a20160512d2016 u| 0 101 0 $aeng 135 $aurnn|008mamaa 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 14$aThe Chemistry of Benzotriazole Derivatives $eA Tribute to Alan Roy Katritzky /$fedited by Jean-Christophe M. Monbaliu 205 $a1st ed. 2016. 210 1$aCham :$cSpringer International Publishing :$cImprint: Springer,$d2016. 215 $a1 online resource (XI, 289 p. 431 illus., 19 illus. in color.) 225 1 $aTopics in Heterocyclic Chemistry,$x1861-9282 ;$v43 311 $a3-319-31552-8 327 $aPreparation, properties and utility of simple benzotriazole derivatives -- Acylbenzotriazoles: new allies for short linear and cyclic peptide constructs -- Benzotriazole-based strategies towards peptidomimetics, conjugates and other peptide derivatives -- Benzotriazole-mediated synthesis of oxygen containing heterocycles -- Benzotriazole-mediated synthesis of nitrogen containing heterocycles -- Benzotriazole: much more than just synthetic heterocyclic chemistry. 330 $aThe series Topics in Heterocyclic Chemistry presents critical reviews on present and future trends in the research of heterocyclic compounds. Overall the scope is to cover topics dealing with all areas within heterocyclic chemistry, both experimental and theoretical, of interest to the general heterocyclic chemistry community. The series consists of topic related volumes edited by renowned editors with contributions of experts in the field. All chapters from Topics in Heterocyclic Chemistry are published Online First with an individual DOI. In references, Topics in Heterocyclic Chemistry is abbreviated as Top Heterocycl Chem and cited as a journal. 410 0$aTopics in Heterocyclic Chemistry,$x1861-9282 ;$v43 606 $aBioorganic chemistry 606 $aCarbohydrates 606 $aMedicinal chemistry 606 $aBioorganic Chemistry$3https://scigraph.springernature.com/ontologies/product-market-codes/C19010 606 $aCarbohydrate Chemistry$3https://scigraph.springernature.com/ontologies/product-market-codes/C19030 606 $aMedicinal Chemistry$3https://scigraph.springernature.com/ontologies/product-market-codes/C28000 615 0$aBioorganic chemistry. 615 0$aCarbohydrates. 615 0$aMedicinal chemistry. 615 14$aBioorganic Chemistry. 615 24$aCarbohydrate Chemistry. 615 24$aMedicinal Chemistry. 676 $a572 702 $aMonbaliu$b Jean-Christophe M$4edt$4http://id.loc.gov/vocabulary/relators/edt 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910768162203321 996 $aThe Chemistry of Benzotriazole Derivatives$93655306 997 $aUNINA