LEADER 05286nam 2200673Ia 450 001 9910830648403321 005 20170815110139.0 010 $a1-282-30160-8 010 $a9786612301605 010 $a0-470-18682-8 010 $a0-470-18832-4 035 $a(CKB)1000000000376540 035 $a(EBL)469085 035 $a(OCoLC)609847800 035 $a(SSID)ssj0000353967 035 $a(PQKBManifestationID)11249009 035 $a(PQKBTitleCode)TC0000353967 035 $a(PQKBWorkID)10302259 035 $a(PQKB)11076582 035 $a(MiAaPQ)EBC469085 035 $a(PPN)241414458 035 $a(EXLCZ)991000000000376540 100 $a20731212d1966 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$hPart one$b[electronic resource] /$fDavid S. Breslow, Herman Skolnik 205 $a99th ed. 210 $aNew York $cInterscience$d1966 215 $a1 online resource (635 p.) 225 1 $aChemistry of heterocyclic compounds ;$v21/1 300 $aDescription based upon print version of record. 311 $a0-470-38195-7 320 $aIncludes bibliographies. 327 $aMULTI-SULFUR AND SULFUR AND OXYGEN FIVE- AND SIXMEMBERED HETEROCYCLES; CONTENTS OF PART ONE; 1. C2O2S Ring Systems; I. C2O2S 1, 3, 2-Dioxathiolane and 1, 3, 2-Dioxathiole; A. Sulfite Esters of 1, 2-Glycols; 1. Preparation; 2. Structure and Physical Properties; 3. Reactions; 4. Uses; B. Sulfate Esters of 1, 2-Glycols; 1. Preparation; 2. Structure and Reactions; C. Sulfate Esters of Enediols; D. 1, 3, 2-Dioxathiolan-4-one 2-Oxides; II. C4-C2O2S 2, 4-Dioxa-3-thiabicyclo[3. 2. 0]heptane; III. C2O2S-C2O2S 1, 3, 2-Dioxathiolo[1, 3, 2]dioxathiole Glyoxal Sulfate 327 $aIV. C2O2S-C4O Furo[3, 4-d]-l, 3, 2-dioxathioleV. C2O2S-C4S Thieno[3, 4-d]-1, 3, 2-dioxathiole; VI. C2O2S-C5 3aH-Cyclopenta-1, 3, 2-dioxathiole; VII. C2O2S-C5O 4H-Pyrano[3, 4-d]-1, 3, 2-dioxathiole; VIII. C2O2S-C6 1, 3, 2-Benzodioxathiole; A. Sulfite Esters; B. Sulfate Esters; IX. C2O2S-C7 4H-Cyclohepta-1, 3, 2-dioxathiole; X. C2O2S-C4O-C4O 1, 7, 11, 13-Tetraoxa-12-thiadispiro-[4. 0. 4. 3]trideca-3, 9-diene-2, 8-dione; XI. C2O2S-C4N-C5N 6H-Cyclohepta-1, 3, 2-dioxathiol-4, 8-imine; XII. C2O2S-C5-C6 8H-Indeno[1, 2-d}-1, 3, 2-dioxathiole 327 $aXIII. C2O2S-C4O2-C50 4H, 6H-1, 3, 2-Dioxathiolo[4, 5]-pyrano[3, 2-d]-m-dioxinXIV. C2O2S-C6C6; A. Naphtho[1, 2-d}-1, 3, 2-dioxathiole; B. Naphtho[2, 3-d]-1, 3, 2-dioxathiole; XV. C2O2S-C6-C6-C6; A. Anthra[1, 2-d]-1, 3, 2-dioxathiole; 1. Sulfite Esters; 2. Sulfate Esters; B. Anthra[2, 3-d]-1, 3, 2-dioxathiole; C. Phenanthro[9, 10-d]-1, 3, 2-dioxathiole; XVI. C2O2S-C4N-C4N-C9O2 [1, 3, 2]Dioxathiolo-[4', 5' : 8, 9][1, 6]dioxacycloundeca[2, 3, 4-gh]-pyrrolizine; XVII. C2O2S-C4N-C4N-C10O2 Spiro[1, 6]dioxacyclododeca-[2, 3, 4-gh]-pyrrolizine-9(8H), 4'-[ 1, 3, 2]-dioxathiolane 327 $aXVIII. C2O2S-C5-C6-C6-C6A. Cyclopenta[1, 2]phenanthro[4, 4a-d][1, 3, 2]-dioxathiole; B. Cyclopenta[1, 2]phenanthro[1, 10a-d][1, 3, 2]-dioxathiole; XIX. C2O2S-C6-C6-C6-C6; A. Chryseno[5, 6-d]-1, 3, 2-dioxathiole; B. 4, 9-o-Benzenonaphtho[2, 3-d]-1, 3, 2-dioxathiole; XX. C2O2S-C4O-C4O-C5-C6-C6 3H, 9H-11b, 13a-Epoxycyclopenta[1, 2]phenanthro[4, 4a-d][1, 3, 2]dioxathiole; 2. C2OS2 Ring Systems; I. 1, 2, 5-Oxadithia Compounds; A. C2OS2 1, 2, 5-Oxadithiolane; B. C2OS2-C4SThieno[3, 4-c][1, 2, 5]oxadithiole; C. C2OS2-C6 2, 1, 3-Benzoxadithiole; D. C2OS2-C6-C6 Naphth[1, 2-c][1, 2, 5]oxadithiole 327 $aII. 1, 3, 4-Oxadithia CompoundsC2OS2 1, 3, 4-Oxadithiolane; 3. C2S3 Ring Systems; I. 1, 2, 3-Trithia Compounds; A. C2S3 1,2,3-Trithiole; B. C2S3-C6 Benzotrithiole; C. C2S3-C4N2-C6 Trithiolo[4, 5-b]quinoxaline; II. 1, 2, 4-Trithia Compounds; A. C2S3 1, 2, 4-Trithiolane; B. Spiro Derivatives of 1, 2, 4-Trithiolane; 4. C3OS Ring Systems; I. 1, 2-Oxathia Compounds; A. C3OS 5H-1, 2-Oxathiole, 3H-1, 2-Oxathiole, and 1, 2-Oxathiolane; 1. 3H-1, 2-Oxathiole; 2. 5H-1, 2-Oxathiole; 3. 1, 2-Oxathiolane; a. 1, 2-Oxathiolane 2, 2-Dioxide; (1) Preparation; (a) From 3-Chloroalkanesulfonic Acids 327 $a(b) From 3-Hydroxyalkanesulphonic Acids 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 ;$v21/1. 606 $aOrganosulfur compounds 606 $aHeterocyclic compounds 615 0$aOrganosulfur compounds. 615 0$aHeterocyclic compounds. 676 $a547.594 676 $a547/.59/05 700 $aBreslow$b David Samuel$f1916-$0893559 701 $aSkolnik$b Herman$0893560 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910830648403321 996 $aMulti-sulfur and sulfur and oxygen five- and six-membered heterocycles$91996096 997 $aUNINA