Storr / Gilchrist / Begtrup Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol. 13

Five-Membered Hetarenes with Three or More Heteroatoms
1. Auflage 2014
ISBN: 978-3-13-171851-8
Verlag: Thieme
Format: PDF
Kopierschutz: Adobe DRM (»Systemvoraussetzungen)

E-Book, Englisch, 1010 Seiten, PDF, Format (B × H): 170 mm x 240 mm

Reihe: Science of Synthesis

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 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. This unique resource is designed to be the first point of reference when searching for a synthesis strategy.
- Contains the expertise of presently 450 leading chemists worldwide. - Critically evaluates the preparative applicability and significance of the synthetic methods. - Discusses relevant background information and provides detailed experimental procedures

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

Zielgruppe

Wissenschaftler

Autoren/Hrsg.

Begtrup, Mikael

Bellus, Daniel

Bradley, Paul

Storr, Richard C.

Gilchrist, Thomas L.

Fachgebiete

• Naturwissenschaften Chemie Organische Chemie

Inhaltsverzeichnis

13.1 Product Class 1: 1,2,5-Oxathiazoles, 1,2,3-Dithiazoles, and Related Compounds
13.2 Product Class 2: 1,2,4-Dioxazoles, 1,2,4-Oxathiazoles, and 1,2,4-Dithiazoles
13.3 Product Class 3: 1,3,2-Oxathiazoles, 1,3,2-Dithiazoles, and Related Compounds
13.4 Product Class 4: 1,4,2-Oxathiazoles and Related Compounds
13.5 Product Class 5: 1,2,3-Oxadiazoles
13.6 Product Class 6: 1,2,4-Oxadiazoles
13.7 Product Class 7: 1,2,5-Oxadiazoles
13.8 Product Class 8: 1,3,4-Oxadiazoles
13.9 Product Class 9: 1,2,3-Thiadiazoles
13.10 Product Class 10: 1,2,4-Thiadiazoles
13.11 Product Class 11: 1,2,5-Thiadiazoles and Related Compounds
13.12 Product Class 12: 1,3,4-Thiadiazoles
13.13 Product Class 13: 1,2,3-Triazoles
13.14 Product Class 14: 1,2,4-Triazoles
13.15 Product Class 15: Dithiaphospholes and Their Analogues
13.16 Product Class 16: Oxazaphospholes and Thiazaphospholes
13.17 Product Class 17: Oxadiphospholes and Their Analogues
13.18 Product Class 18: Diazaphospholes and Diazarsoles
13.19 Product Class 19: Azadiphospholes and Their Analogues
13.20 Product Class 20: Triphospholes and Diphospharsoles
13.21 Product Class 21: Thiadiazaphospholes
13.22 Product Class 22: Triazaphospholes
13.23 Product Class 23: Diazadiphospholes
13.24 Product Class 24: Tetraphospholes
13.25 Product Class 25: Tetraazaphospholes
13.26 Product Class 26: Pentaphospholes and Pentarsoles
13.27 Product Class 27: Selenazoles and Tellurazoles Containing One or More Other Heteroatoms
13.28 Product Class 28: Oxatriazoles
13.29 Product Class 29: Thiatriazoles
13.30 Product Class 30: Tetrazoles
13.31 Product Class 31: Pentazoles

Über Autor(innen)

Richard C. Storr, Tom L. Gilchrist