LEADER 05651nam 2200697Ia 450 001 9910830721503321 005 20230617005258.0 010 $a1-280-23559-4 010 $a9786610235599 010 $a0-470-31848-1 010 $a0-471-74412-3 010 $a0-471-74411-5 035 $a(CKB)1000000000355627 035 $a(EBL)239975 035 $a(OCoLC)475951995 035 $a(SSID)ssj0000122313 035 $a(PQKBManifestationID)11132379 035 $a(PQKBTitleCode)TC0000122313 035 $a(PQKBWorkID)10123460 035 $a(PQKB)11370226 035 $a(MiAaPQ)EBC239975 035 $a(EXLCZ)991000000000355627 100 $a20050411d2005 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aCinnolines and phthalazines$b[electronic resource] $esupplement II /$fD.J. Brown 210 $aHoboken, N.J. $cWiley$dc2005 215 $a1 online resource (499 p.) 225 1 $aChemistry of heterocyclic compounds ;$vv. 64 300 $a"Covers both ring systems for the period 1973-2004 with a comprehensive compilation and discussion of the literature"--P. vii. 300 $aContinues a supplemental review by G.M. Singerman and N.R. Patel in: Condensed pyridazines including cinnolines and phthalazines / edited by Raymond N. Castle. 1973. 311 $a0-471-48587-X 320 $aIncludes bibliographical references (p. 413-443) and index. 327 $aCINNOLINES AND PHTHALAZINES Supplement II; Preface; Contents; CHAPTER 1 PRIMARY SYNTHESES OF CINNOLINES; 1.1 From a Single Carbocyclic Substrate; 1.1.1 By Formation of the N1-C8a Bond; 1.1.2 By Formation of the N1-N2 Bond; 1.1.3 By Formation of the N2-C3 Bond; 1.1.4 By Formation of the C3-C4 Bond; 1.1.5 By Formation of the C4-C4a Bond; 1.2 From a Carbocyclic Substrate and One Synthon; 1.2.1 When the Synthon Supplies N2 of the Cinnoline; 1.2.2 When the Synthon Supplies N1 + N2 of the Cinnoline; 1.2.3 When the Synthon Supplies N2 + C3 of the Cinnoline 327 $a1.2.4 When the Synthon Supplies C3 + C4 of the Cinnoline1.2.5 When the Synthon Supplies N1 + N2 + C3 + C4 of the Cinnoline; 1.3 From a Pyridazine Substrate; 1.4 From Other Heteromonocyclic Substrates; 1.5 From Heterobicyclic Substrates; 1.6 From Heteropolycyclic Substrates; 1.7 Glance Index to Typical Cinnolines Derivatives Available by Primary Syntheses; CHAPTER 2 CINNOLINE, ALKYLCINNOLINES, AND ARYLCINNOLINES; 2.1 Cinnoline; 2.1.1 Preparation of Cinnoline and Hydrocinnolines; 2.1.2 Physical Properties of Cinnoline; 2.1.3 Reactions of Cinnoline; 2.2 Alkyl- and Arylcinnolines 327 $a2.2.1 Preparation of Alkyl- and Arylcinnolines2.2.2 Reactions of Alkyl- and Arylcinnolines; CHAPTER 3 HALOGENOCINNOLINES; 3.1 Preparation of Halogenocinnolines; 3.2 Reactions of Halogenocinnolines; CHAPTER 4 OXYCINNOLINES; 4.1 Tautomeric Cinnolinones; 4.1.1 Preparation of Tautomeric Cinnolinones; 4.1.2 Reactions of Tautomeric Cinnolinones; 4.1.2.1 Alkylation of Tautomeric Cinnolinones; 4.1.2.2 Other Reactions of Tautomeric Cinnolinones; 4.2 Other Oxycinnolines; CHAPTER 5 THIOCINNOLINES; 5.1 Cinnolinethiones; 5.2 Other Thiocinnolines; CHAPTER 6 NITRO-, AMINO-, AND RELATED CINNOLINES 327 $a6.1 Nitrocinnolines6.2 Aminocinnolines and Related Compounds; 6.2.1 Preparation of Amino-, Hydrazino-, and Arylazocinnolines; 6.2.2 Reactions of Amino- and Hydrazinocinnolines; CHAPTER 7 CINNOLINECARBOXYLIC ACIDS AND RELATED DERIVATIVES; 7.1 Cinnolinecarboxylic Acids; 7.1.1 Preparation of Cinnolinecarboxylic Acids; 7.1.2 Reactions of Cinnolinecarboxylic Acids; 7.2 Cinnolinecarboxylic Esters; 7.3 Cinnolinecarboxamides and Cinnolinecarbohydrazides; 7.4 Cinnolinecarbonitriles; 7.5 Cinnoline Aldehydes and Ketones; CHAPTER 8 PRIMARY SYNTHESES OF PHTHALAZINES 327 $a8.1 From a Single Benzene Derivative as Substrate8.1.1 By Formation of the C1-C8a Bond; 8.1.2 By Formation of the C1-N2 Bond; 8.2 From a Benzene Derivative as Substrate and One Synthon; 8.2.1 Where the Synthon Supplies C1 of the Phthalazine; 8.2.2 Where the Synthon Supplies N2 + N3 of the Phthalazine; 8.2.2.1 Using 1,2-Dialkylbenzenes as Substrates; 8.2.2.2 Using 1-Alkyl-2-ketobenzenes as Substrates; 8.2.2.3 Using 1-Alkyl-2-halogenoformylbenzenes as Substrates; 8.2.2.4 Using 1,2-Dialdehydrobenzenes as Substrates; 8.2.2.5 Using 1-Aldehydo-2-ketobenzenes as Substrates 327 $a8.2.2.6 Using 1-Aldehydo-2-carboxybenzenes as Substrates 330 $aThis book provides the most comprehensive, current reference on the synthetic chemistry of cinnolines and phthalazines. Applications to the syntheses of natural products and other chiral compounds are described. Volume 64 contains chapters exploring the following topics:* Primary Syntheses of Cinnolines* Cinnoline, Alklycinnolines, and Arylcinnolines* Halogenocinnolines* Oxycinnolines* Thiocinnolines* Nitro-, Amino-, and Related Cinnolines* Cinnolinecarboxylic Acids and Related Derivatives* Primary Syntheses of Phthalazines* Phthalazine, Alklyphthalazines, a 410 0$aChemistry of heterocyclic compounds ;$vv. 64. 606 $aPyridazines 606 $aOrganic compounds$xSynthesis 606 $aChirality 615 0$aPyridazines. 615 0$aOrganic compounds$xSynthesis. 615 0$aChirality. 676 $a547.2 676 $a547.593 700 $aBrown$b D. J$0383088 701 $aCastle$b Raymond N$g(Raymond Nielson),$f1916-$01606444 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910830721503321 996 $aCinnolines and phthalazines$93932243 997 $aUNINA LEADER 03703nam 2200697 450 001 9910812884903321 005 20201023111955.0 010 $a1-4742-8533-3 010 $a1-4725-6932-6 010 $a1-4725-6931-8 024 7 $a10.5040/9781474285339 035 $a(CKB)3710000000726342 035 $a(EBL)4542873 035 $a(OCoLC)951977324 035 $a(SSID)ssj0001677619 035 $a(PQKBManifestationID)16488550 035 $a(PQKBTitleCode)TC0001677619 035 $a(PQKBWorkID)14958400 035 $a(PQKB)11200591 035 $a(MiAaPQ)EBC4542873 035 $a(OCoLC)1201426283 035 $a(CaBNVSL)mat74285339 035 $a(CaBNVSL)9781474285339 035 $a(EXLCZ)993710000000726342 100 $a20201023d2020 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aAfrican lace-bark in the Caribbean $ethe construction of race, class and gender /$fSteeve O. Buckridge 210 1$aLondon, England :$cBloomsbury Academic, an imprint of Bloomsbury Publishing, Plc,$d2020. 210 2$aLondon, England :$cBloomsbury Publishing,$d2020 215 $a1 online resource (217 p.) 300 $aDescription based upon print version of record. 311 $a1-350-05850-5 311 $a1-4725-6930-X 320 $aIncludes bibliographical references and index. 327 $aPre-history to early slave trade : "people of the forest" -- Plantation Jamaica : "controlling the silver" -- Victorian Jamaica : "fancy fans and doilies". 330 $aIn Caribbean history, the European colonial plantocracy created a cultural diaspora in which African slaves were torn from their ancestral homeland. In order to maintain vital links to their traditions and culture, slaves retained certain customs and nurtured them in the Caribbean. The creation of lace-bark cloth from the lagetta tree was a practice that enabled slave women to fashion their own clothing, an exercise that was both a necessity, as clothing provisions for slaves were poor, and empowering, as it allowed women who participated in the industry to achieve some financial independence. This is the first book on the subject and, through close collaboration with experts in the field including Maroon descendants, scientists and conservationists, it offers a pioneering perspective on the material culture of Caribbean slaves, bringing into focus the dynamics of race, class and gender. Focusing on the time period from the 1660s to the 1920s, it examines how the industry developed, the types of clothes made, and the people who wore them. The study asks crucial questions about the social roles that bark cloth production played in the plantation economy and colonial society, and in particular explores the relationship between bark cloth production and identity amongst slave women. 606 $aTapa$xSocial aspects$zCaribbean Area 606 $aWomen slaves$xClothing$zCaribbean Area 606 $aBlacks$xClothing$zCaribbean Area 606 $aBlacks$xMaterial culture$zCaribbean Area 606 $aClothing and dress$zCaribbean Area$xHistory 606 $aTextile design & theory$2bicssc 615 0$aTapa$xSocial aspects 615 0$aWomen slaves$xClothing 615 0$aBlacks$xClothing 615 0$aBlacks$xMaterial culture 615 0$aClothing and dress$xHistory. 615 7$aTextile design & theory 676 $a391/.208625098611 700 $aBuckridge$b Steeve O.$01714786 801 0$bDLC 801 1$bCaBNVSL 801 2$bCaBNVSL 906 $aBOOK 912 $a9910812884903321 996 $aAfrican lace-bark in the Caribbean$94108902 997 $aUNINA LEADER 01423nas 2200421-a 450 001 996202360803316 005 20240413021611.0 035 $a(CKB)963018322295 035 $a(CONSER)sn-89024092- 035 $a(EXLCZ)99963018322295 100 $a19890328b19uu2010 --- a 101 0 $aeng 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 00$aBank loan report 210 $aNew York, N.Y. $cDealers' Digest, Inc 215 $a1 online resource 300 $aPublished: Securities Data Pub., ; Thomson Media, 311 $aPrint version: Bank loan report. 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