Schaumann / Bellus / Boyd | Science of Synthesis: Houben-Weyl Methods of Molecular Transformations  Vol. 11 | E-Book | sack.de
E-Book

E-Book, Englisch, 1160 Seiten, PDF, Format (B × H): 170 mm x 240 mm

Reihe: Science of Synthesis

Schaumann / Bellus / Boyd Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol. 11

Five-Membered Hetarenes with One Chalcogen and One Additional Heteroatom
1. Auflage 2014
ISBN: 978-3-13-171831-0
Verlag: Thieme
Format: PDF
Kopierschutz: Adobe DRM (»Systemvoraussetzungen)

Five-Membered Hetarenes with One Chalcogen and One Additional Heteroatom

E-Book, Englisch, 1160 Seiten, PDF, Format (B × H): 170 mm x 240 mm

Reihe: Science of Synthesis

ISBN: 978-3-13-171831-0
Verlag: Thieme
Format: PDF
Kopierschutz: Adobe DRM (»Systemvoraussetzungen)



Turning Information into Knowledge

Science of Synthesis: Houben-Weyl Methods of Molecular Transformations is the entirely new edition of the acclaimed reference series, Houben-Weyl, the standard synthetic chemistry resource since 1909. This new edition is published in English and will comprise of 48 volumes published between the years 2000 and 2008.

Science of Synthesis is a quality reference work developed by a highly esteemed editorial board to provide a comprehensive and critical selection of reliable organic and organometallic synthetic methods. Science of Synthesis is designed to be the first point of reference when searching for a synthesis strategy.

This volume is the third in Category 2 (Hetarenes and Related Ring Systems) of Science of Synthesis and deals with five-membered hetarenes with one chalcogen and one additional heteroatom. Throughout this category, a hetarene is considered to be a heterocyclic ring with a fully conjugated perimeter of pi- or nonbonding electrons. Additionally, potentially tautomeric systems with a hydroxy, sulfanyl, or amino substituent are included when conjugation is possible at least in one tautomer. In the Volume 11, this formal definition leads to quite different types of five-membered heterocyclic ring systems including the 1,2- or 1,3-arrangement of two chalcogen atoms to give cationic rings, as well as 1,2- or 1,3-combinations of a chalcogen atom and a nitrogen or phosphorus atom. The latter group comprises well-known ring systems such as oxazoles or thiazoles, but also less well-studied ring systems.

For full information on the Science of Synthesis series, visit the Science of Synthesis Homepage. Series Editors: D. Bellus, S. V. Ley, R. Noyori, M. Regitz, E. Schaumann, I. Shinkai, E. J. Thomas, B. M. Trost, P. J. Reider

Schaumann / Bellus / Boyd Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol. 11 jetzt bestellen!

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11.1 Product Class 1: 1,3-Dioxolium Salts and Annulated Analogues11.2 Product Class 2: 1,2-Oxathiolium Salts11.3 Product Class 3: 1,3-Oxathiolium Salts and Related Compounds11.4 Product Class 4: 1,2-Oxaselenolium Salts11.5 Product Class 5: 1,3-Oxaselenolium Salts11.6 Product Class 6: 1,2-Oxatellurolium Compounds and Benzoannulated Analogues11.7 Product Class 7: 1,2-Dithiolium Salts and Related Compounds11.8 Product Class 8: 1,3-Dithiolium Salts, Se and Te Analogues, and Benzoannulated Analogues11.9 Product Class 9: Isoxazoles11.10 Product Class 10: 1,2-Benzisoxazoles and Related Compounds11.11 Product Class 11: 2,1-Benzisoxazoles and Related Compounds11.12 Product Class 12: Oxazoles11.13 Product Class 13: Benzoxazoles and Other Annulated Oxazoles11.14 Product Class 14: 1,3-Oxaphospholes and Benzoannulated Analogues11.15 Product Class 15: Isothiazoles11.16 Product Class 16: Benzisothiazoles11.17 Product Class 17: Thiazoles11.18 Product Class 18: Benzothiazoles and Related Compounds11.19 Product Class 19: 1,2- and 1,3-Thiaphospholes and Benzoannulated Analogues11.20 Product Class 20: Isoselenazoles11.21 Product Class 21: Annulated Isoselenazole Compounds11.22 Product Class 22: Selenazoles11.23 Product Class 23: Annulated Selenazole Compounds11.24 Product Class 24: 1,3-Selenaphospholes11.25 Product Class 25: Isotellurazoles, and Annulated Isotellurazole and Tellurazole Compounds


Ernst Schaumann



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