LEADER 05286nam 2200673Ia 450 001 9910144284003321 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. 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