Detailed table of contents (pdf)

Detailed table of contents (pdf) Detailed table of contents (pdf)

thieme.chemistry.com
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X Table of Contents 17.4.4 Product Subclass 4: Benzothiepins and Selenium/Tellurium Analogues A. L. Schwan ............................................................. 717 17.4.5 Product Subclass 5: Azepines, Cyclopentazepines, and Phosphorus Analogues M. D. Surman and R. H. Hutchings ......................................... 749 17.4.6 Product Subclass 6: Benzazepines and Their Group 15 Analogues J.-P. K. Meigh ............................................................. 825 17.5 Product Class 5: Seven-Membered Hetarenes with Two or More Heteroatoms R. J. Herr ................................................................. 929 17.6 Product Class 6: Eight- and Nine-Membered Hetarenes and Heteroannulenes with One or More Heteroatoms R. M. Borzilleri ............................................................ 979 17.7 Product Class 7: Cyclazines Y. Tominaga ............................................................. 1025 17.8 Product Class 8: Porphyrins and Related Compounds K. M. Smith and M. G. H. Vicente ......................................... 1081 17.9 Product Class 9: Phthalocyanines and Related Compounds N. B. McKeown .......................................................... 1237 Keyword Index ......................................................... 1369 Author Index ........................................................... 1417 Abbreviations .......................................................... 1495

Table of Contents XI Table of Contents Introduction S. M. Weinreb and Y. R. Mahajan Introduction ............................................................ 1 17.1 Product Class 1: Six-Membered Hetarenes with Two Unlike Heteroatoms 17.1.1 Product Subclass 1: Two Unlike Oxygen, Sulfur, Selenium, or Tellurium Atoms S. Yamazaki and K. Yamamoto 17.1.1 Product Subclass 1: Two Unlike Oxygen, Sulfur, Selenium, or Tellurium Atoms ....................................................... 19 17.1.1.1 1,4-Oxathiins .............................................................. 21 17.1.1.1.1 Synthesis by Ring-Closure Reactions ........................................ 21 17.1.1.1.1.1 Method 1: Reaction of Sulfur Dichloride with Divinyl Ether .............. 21 17.1.1.1.2 Synthesis by Ring Transformation ........................................... 22 17.1.1.1.2.1 Method 1: Rearrangement of 1,3-Oxathiolanes ......................... 22 17.1.1.1.3 Aromatization ............................................................. 22 17.1.1.1.3.1 Method 1: Dehydrochlorination ....................................... 22 17.1.1.1.3.2 Method 2: Pummerer Reaction ........................................ 22 17.1.1.1.4 Synthesis by Substituent Modification ...................................... 23 17.1.1.1.4.1 Addition of Heteroatoms .................................................. 23 17.1.1.1.4.1.1 Method 1: Oxidation of a Ring Sulfur .................................. 23 17.1.1.1.4.2 Modification of Substituents ............................................... 24 17.1.1.1.4.2.1 Method 1: Condensation Reaction of the Carboxy Group with Aniline Derivatives ................................................ 24 17.1.1.2 Annulated 1,4-Oxathiins ................................................... 24 17.1.1.2.1 Synthesis by Ring-Closure Reactions ........................................ 24 17.1.1.2.1.1 By Annulation to an Arene ................................................. 24 17.1.1.2.1.1.1 By Formation of Three Heteroatom—Carbon Bonds .......................... 24 17.1.1.2.1.1.1.1 Fragments O—C—C, C—C, and S ............................................ 24 17.1.1.2.1.1.1.1.1 Method 1: Reaction of Monoimines with Phosphorus Pentasulfide ....... 24 17.1.1.2.1.1.2 By Formation of Two Heteroatom—Carbon Bonds ........................... 25 17.1.1.2.1.1.2.1 Fragments S—C—C—O and C—C ............................................ 25 17.1.1.2.1.1.2.1.1 Method 1: Reactions Involving Nucleophilic Sulfur and Oxygen .......... 25 17.1.1.2.1.1.2.1.2 Method 2: Cycloaddition Reactions .................................... 27 17.1.1.2.1.1.2.2 Fragments S—C—C and O—C—C ............................................ 28

X Table <strong>of</strong> Contents<br />

17.4.4 Product Subclass 4: Benzothiepins and Selenium/Tellurium Analogues<br />

A. L. Schwan ............................................................. 717<br />

17.4.5 Product Subclass 5: Azepines, Cyclopentazepines,<br />

and Phosphorus Analogues<br />

M. D. Surman and R. H. Hutchings ......................................... 749<br />

17.4.6 Product Subclass 6: Benzazepines and Their Group 15 Analogues<br />

J.-P. K. Meigh ............................................................. 825<br />

17.5 Product Class 5: Seven-Membered Hetarenes with Two or More<br />

Heteroatoms<br />

R. J. Herr ................................................................. 929<br />

17.6 Product Class 6: Eight- and Nine-Membered Hetarenes and<br />

Heteroannulenes with One or More Heteroatoms<br />

R. M. Borzilleri ............................................................ 979<br />

17.7 Product Class 7: Cyclazines<br />

Y. Tominaga ............................................................. 1025<br />

17.8 Product Class 8: Porphyrins and Related Compounds<br />

K. M. Smith and M. G. H. Vicente ......................................... 1081<br />

17.9 Product Class 9: Phthalocyanines and Related Compounds<br />

N. B. McKeown .......................................................... 1237<br />

Keyword Index ......................................................... 1369<br />

Author Index ........................................................... 1417<br />

Abbreviations .......................................................... 1495

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