de Meijere / Banert / Bellus | Science of Synthesis: Houben-Weyl Methods of Molecular Transformations  Vol. 24 | E-Book | sack.de
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E-Book, Englisch, 1194 Seiten, PDF, Format (B × H): 170 mm x 240 mm

Reihe: Science of Synthesis

de Meijere / Banert / Bellus Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol. 24

Three Carbon-Heteroatom Bonds: Ketene Acetals and Yne-X Compounds

E-Book, Englisch, 1194 Seiten, PDF, Format (B × H): 170 mm x 240 mm

Reihe: Science of Synthesis

ISBN: 978-3-13-171981-2
Verlag: Thieme
Format: PDF
Kopierschutz: Adobe DRM (»Systemvoraussetzungen)



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 400 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.
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24.1 Product Class 1: 1,1-Bis(heteroatom-functionalized) Allenes
24.1.1 Product Subclass 1: 1,1-Dihaloallenes
24.1.2 Product Subclass 2: 1-Halo-1-(organooxy)allenes
24.1.3 Product Subclass 3: 1-Halo-1-(organochalcogeno)allenes and 1-Halo-1-(organochalcogeno)butatrienes
24.1.4 Product Subclass 4: 1-Nitrogen-Functionalized 1-Haloallenes
24.1.5 Product Subclass 5: 1-Phosphorus-Functionalized 1-Haloallenes
24.1.6 Product Subclass 6: 1,1-Bis(organooxy)allenes, 1,1-Bis(organooxy)butatrienes, 1-(Organooxy)-1-siloxyallenes, and 1-(Organooxy)allen-1-olates
24.1.7 Product Subclass 7: 1-(Organochalcogeno)-1-(organooxy)allenes
24.1.8 Product Subclass 8: 1-Nitrogen-Functionalized 1-(Organooxy)allenes and Allen-1-olates
24.1.9 Product Subclass 9: 1-Phosphorus-Functionalized 1-(Organooxy)allenes-Siloxyallenes
24.1.10 Product Subclass 10: 1,1-Bis(organochalcogeno)allenes and 1,1-Bis(organochalcogeno)butatrienes
24.1.11 Product Subclass 11: 1-Nitrogen-Functionalized 1-(Organochalcogeno)allenes
24.1.12 Product Subclass 12: 1-Phosphorus-Functionalized 1-(Organochalcogeno)allenes
24.1.13 Product Subclass 13: 1,1-Bis(nitrogen-functionalized) Allenes and Butatrienes
24.1.14 Product Subclass 14: 1-Nitrogen-Functionalized 1-Phosphorus-Functionalized Allenes
24.1.15 Product Subclass 15: 1,1-Bis(phosphorus-functionalized) Allenes
24.2 Product Class 2: 1,1-Bis(heteroatom-functionalized) Alk-1-enes
24.2.1 Product Subclass 1: 1,1-Dihaloalk-1-enes
24.2.2 Product Subclass 2: 1-Halo-1-(organooxy)alk-1-enes
24.2.3 Product Subclass 3: 1-Halo-1-(organochalcogeno)alk-1-enes
24.2.4 Product Subclass 4: 1-Nitrogen-Functionalized 1-Haloalk-1-enes
24.2.5 Product Subclass 5: 1-Phosphorus-Functionalized 1-Haloalk-1-enes
24.2.6 Product Subclass 6: 1,1-Bis(organooxy)alk-1-enes
24.2.7 Product Subclass 7: 1-(Organooxy)-1-(organosulfanyl)alk-1-enes
24.2.8 Product Subclass 8: 1-(Organooxy)-1-(organoselanyl)- and 1-(Organooxy)-1-(organotellanyl)alk-1-enes
24.2.9 Product Subclass 9: 1-Nitrogen-Functionalized 1-(Organooxy)alk-1-enes (Ketene O,N-Acetals)
24.2.10 Product Subclass 10: 1-Phosphorus-Functionalized 1-(Organooxy)alk-1-enes
24.2.11 Product Subclass 11: 1,1-Bis(organosulfanyl)alk-1-enes (Ketene S,S-Acetals)
24.2.12 Product Subclass 12: 1-(Organoselanyl)-1-(organosulfanyl)alk-1-enes and 1-(Organosulfanyl)-1-(organotellanyl)alk-1-enes
24.2.13 Product Subclass 13: 1-Nitrogen-Functionalized 1-(Organosulfanyl)alk-1-enes
24.2.14 Product Subclass 14: 1-Phosphorus-Functionalized 1-(Organosulfanyl)alk-1-enes
24.2.15 Product Subclass 15: 1,1-Bis(organoselanyl)alk-1-enes and Derivatives
24.2.16 Product Subclass 16: 1,1-Bis(organotellanyl)alk-1-enes and Derivatives
24.2.17 Product Subclass 17: 1,1-Bis(nitrogen-functionalized) Alk-1-enes
24.2.17.1 Alk-1-ene-1,1-diamines
24.2.17.2 Alk-1-ene-1,1-diamines with Retention of the Functional Group
24.2.17.3 1,1-Bisazo-, 1,1-Diazido-, and 1,1-Dinitroalk-1-enes
24.2.18 Product Subclass 18: 1-Nitrogen-Functionalized 1-Phosphorus-Functionalized Alk-1-enes
24.2.19 Product Subclass 19: 1,1-Bis(phosphorus-functionalized) Alk-1-enes
24.3 Product Class 3: Bis(heteroatom-functionalized) Acetylenes
24.3.1 Product Subclass 1: Dihaloacetylenes
24.3.2 Product Subclass 2: 1-Heteroatom-Functionalized 2-Haloacetylenes
24.3.3 Product Subclass 3: Bis(organooxy)acetylenes
24.3.4 Product Subclass 4: 1-(Organochalcogeno)-2-(organooxy)acetylenes
24.3.5 Product Subclass 5: 1-Nitrogen-Functionalized 2-(Organooxy)acetylenes
24.3.6 Product Subclass 6: 1-Phosphorus-Functionalized 2-(Organooxy)acetylenes
24.3.7 Product Subclass 7: Bis(organochalcogeno)acetylenes
24.3.8 Product Subclass 8: 1-Nitrogen-Functionalized 2-(Organochalcogeno)acetylenes
24.3.9 Product Subclass 9: 2-Phosphorus-Functionalized 1-(Organochalcogeno)acetylenes
24.3.10 Product Subclass 10: Bis(nitrogen-functionalized) Acetylenes
24.3.11 Product Subclass 11: 1-Nitrogen-Functionalized 2-Phosphorus-Functionalized Acetylenes and Bis(phosphorus-functionalized) Acetylenes
24.4 Product Class 4: 1-Heteroatom-Functionalized Alk-1-ynes
24.4.1 Product Subclass 1: 1-Haloalk-1-ynes and Alk-1-yn-1-ols
24.4.2 Product Subclass 2: 1-(Organooxy)alk-1-ynes and 1-(Heterooxy)alk-1-ynes
24.4.3 Product Subclass 3: 1-(Organosulfanyl)-, 1-(Organoselanyl)-, and 1-(Organotellanyl)alk-1-ynes
24.4.4 Product Subclass 4: 1-Nitrogen-Functionalized Alk-1-ynes
24.4.4.1 Alk-1-yn-1-amines
24.4.4.2 N-Acyl- and N-Sulfonylalk-1-yn-1-amines
24.4.4.3 Alk-1-ynyldiazonium Salts, 1-Azidoalk-1-ynes, and 1-Nitroalk-1-ynes
24.4.5 Product Subclass 5: 1-Phosphorus-Functionalized Alk-1-ynes


Armin de Meijere, Ernst Schaumann


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