LEADER 05341nam 2200673 450 001 9910830898903321 005 20220307143555.0 010 $a1-282-30161-6 010 $a9786612301612 010 $a0-470-18683-6 010 $a0-470-18833-2 035 $a(CKB)1000000000376541 035 $a(EBL)469086 035 $a(OCoLC)689995572 035 $a(SSID)ssj0000353968 035 $a(PQKBManifestationID)11236648 035 $a(PQKBTitleCode)TC0000353968 035 $a(PQKBWorkID)10302236 035 $a(PQKB)10334247 035 $a(MiAaPQ)EBC469086 035 $a(MiAaPQ)EBC5215025 035 $a(Au-PeEL)EBL5215025 035 $a(PPN)241417619 035 $a(EXLCZ)991000000000376541 100 $a20220307d1966 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aMulti-sulfur and sulfur and oxygen five-and six-membered heterocycles$hVolume 21$iPart 2 /$fDavid S. Breslow, Herman Skolnik 205 $a99th ed. 210 1$aNew York :$cInterscience Publishers,$d[1966] 210 4$dİ1966 215 $a1 online resource (814 p.) 225 1 $aChemistry of Heterocyclic Compounds ;$vVolume 21 300 $aDescription based upon print version of record. 311 $a0-470-38196-5 320 $aIncludes bibliographies. 327 $aMULTI-SULFUR AND SULFUR AND OXYGEN FIVE- AND SIX-MEMBERED HETEROCYCLES; CONTENTS OF PART TWO; 6. C24S2 Ring Systems; I. C2O2S2; A. 1,3, 2,4-Dioxadithiane; 1. Preparation; 2. Mechanism of Formation; 3. Reactions; B. 1,3,2,4-Dioxadithiin; II. C,-C202S, 5H-Cyclopenta-l,3,2,4 -dioxaclithiin; III. Cz02S2-Cz0,S2 1,3,2,4-Dioxadithihd5,6- 1,3,2,4-dioxadithh .; IV. C,O, -C, 1,3,2,4 -Benzodioxadithiin; 7. C8S4 Ringsystems; I. C2S4; A. s-Tetrathiane; B. Spiro Derivatives; 1. C,-C,-C S, 6,7,13,14-Tetrathiadispiro f4.2.4.2jL-tetradecane; 2. C2S4-C,-C, 7,8,15,16-Tetrathiadispiro [5.2.5.2]-hexadecane 327 $aII. C,N,S-C2S4 2,3,4,8-Tetrathia-6, '7-diazabicyclo 13.2.11 octane8. C,O,SRingSystems; I. 1,3,2-Dioxathia Compounds; A. CSO2S; 1. lY3,2-Dioxathiane; a. Sulfite Esters; (1) Preparation; (2) Structure and Physical Properties; (3) Reactions; b. Sulfate Esters; (1) Preparation and Properties; (2) Reactions; c. Spiro Derivatives; 2. 4H- 1,3,2-Dioxathiin; B. C,0-C302S 4H-Fur43,2-d]-l1 3,2-dioxathiin; C. C3O2S-C5O; 1. 4H, 8H-Pyrano(3, 2-d]-1,3, 2-dioxathiin; 2. 48,5H-Pyran44,3-d]-1,3,2-dioxathiin; D. c@~s-c6-c, Naphthdl, 8-de]-1,3,2-dioxathiin; E. c,o2s-c6-c,-c6; 1. Anthrdl, 9-de]-1,3,2-dioxathiin 327 $a2. 4,10-Ethan0-4H-11aphthtZ, 3-d]-1,3,2- dioxathiin3. Decahydro-5,9-methanobenzocycl&tene-4a, 11 (W)-diol Cyclic Sulfite; F. Cyclic Sulfites of Steroids and Related Com- pounds; II. 1,3,4-Dimthia Compounds C,O,S-C, 2,4,1- Benzodioxathiin; IIl. 1,3, 5-Dioxathia Compounds C302S 1,3,5- Dioxathiane; 9. C3OS2 Ring Systems; I. 1,2,6-Oxadithia Compounds; A. C3W2 1,2,6-Oxadithiane and 3H-1,2,6-oxadithiin; 1. 1,2,6-0xadithiane; 2. 3H-1,2,6-Oxadithiin; B. c@8,-C,-c6 Naphwl, B - c ~ ] [I, 2,610xadithiin; II. 1,2,4-Oxadithia Compounds; C3oS2 1,2,4-Oxadithiane; III. 1,3,4-oxadithia Compounds 327 $aC,06,-C6 -C, Naphth[ 1,2-e] [ 1,3,4]oxadithiin and Spiro [naphthalene-1(W), 3'-naphtMl, 2-e] [ 1,3,4]oxadithiin]IV. 1,3,5dkadithia Compounds; C,OS, 1,3, fi-oxadithiane; 10. C3S3 Ring Systems; I. 1,2,3-Trithia Compounds 1,2,3-Trithiane and Related Spiro Derivatives; II. 1,3,5-Trithia Compounds; A. s-Trithiane; 1. Preparation; 2. Structure; 3. Reactions; a. General Properties; b. Complexes with Heavy Metal Salts; c. Thermal Reactions; d. Halogenation'; e. Oxidation; f. Miscellaneous Reactions; g. Methylene Derivative; 4. Uses; B. C,S,-C@,-C,S, 2,4,6,8,9,10-HWthia-adarnantane 327 $aC. C,S,-C,NS-C,NS 4,6,1O-Trithia-l-azaadaman-tane11. C4O6 Ring Systems; I. o-Oxathia Compounds; A. C,oS o-Oxathiane and o-oxathiin; 1. o-Oxathiane; a. Preparation; b. Properties, Reactions, and Uses; 2. Dihydro-o-oxathiin; 3. o-Oxathiin; B. C,-C,OS 5H-Cyclopentfc] [ 1,210xathiin; C. C4OS-C6; 1. l,%-Benzoxathiin; 2. 2,l-Benzoxathiin; 3. 2,3-Benzoxathiin; D. C4oS-C,-C6; 1. W-NaphNl, 2-4-2, &oxathiin; 2. 3H-Naphtql, 8-cd]-[lJ 2I-oxathiin; 3. Dibenz[ ce]-[ 1, 21 -oxathiin; E. c,~-c6-c6-c6; 1. Benzo[c]aaphth[2,l-e]-[ 1,2]-01mthiin 327 $a2. Benzo[c]naphth[1, 2-e]-[1, 2]-oxathiin and Benzo[c]naphth[2, 3-e]-[1, 2]-oxathiin 330 $aChemistry of Heterocyclic Compounds publishes articles, letters to the Editor, reviews, and minireviews on the synthesis, structure, reactivity, and biological activity of heterocyclic compounds including natural products. The journal covers investigations in heterocyclic chemistry taking place in scientific centers of all over the world, including extensively the scientific institutions in Russia, Ukraine, Latvia, Lithuania and Belarus. 410 0$aChemistry of heterocyclic compounds ;$vVolume 21. 606 $aOrganosulfur compounds 615 0$aOrganosulfur compounds. 676 $a547.06 700 $aBreslow$b David S.$01214833 702 $aSkolnik$b Herman 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910830898903321 996 $aMulti-sulfur and sulfur and oxygen five-and six-membered heterocycles$92805017 997 $aUNINA LEADER 01524oam 2200433zu 450 001 9910375808803321 005 20210807002222.0 035 $a(CKB)3170000000004029 035 $a(SSID)ssj0000812534 035 $a(PQKBManifestationID)12368954 035 $a(PQKBTitleCode)TC0000812534 035 $a(PQKBWorkID)10878586 035 $a(PQKB)11599843 035 $a(Association for Computing Machinery)10.1145/1595836 035 $a(EXLCZ)993170000000004029 100 $a20160829d2009 uy 101 0 $aeng 135 $aurnn|008mam|a 181 $ctxt 182 $cc 183 $acr 200 00$aProceedings of the 2nd International Workshop on Social Software Engineering and Applications 210 31$a[Place of publication not identified]$cAssociation for Computing Machinery$d2009 215 $a1 online resource (40 p.;) 225 1 $aACM Conferences 300 $aBibliographic Level Mode of Issuance: Monograph 311 $a1-60558-682-X 410 0$aACM Conferences 517 3 $aSoSEA '09 606 $aInformation Technology$xComputer Science (Hardware & Networks) 615 4$aInformation Technology$xComputer Science (Hardware & Networks) 700 $aHammouda$b Imed$0855705 702 $aHammouda$b Imed 712 02$aAssociation for Computing Machinery-Digital Library. 801 0$bPQKB 906 $aBOOK 912 $a9910375808803321 996 $aProceedings of the 2nd International Workshop on Social Software Engineering and Applications$92264451 997 $aUNINA