Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol. 32: X-Ene-X (X=F, Cl, Br, I, O, S, Se, Te, N, P), Ene-Hal, and Ene-O Compounds

by J. Mulzer (Editor)

Overview

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.

Product Details

ISBN-13:	9783131782717
Publisher:	Thieme
Publication date:	05/14/2014
Series:	Science of Synthesis , #32
Sold by:	Barnes & Noble
Format:	eBook
Pages:	914
File size:	34 MB
Note:	This product may take a few minutes to download.

Table of Contents

32.1 Product Class 1: 1,3-Bis(heteroatom-substituted) Allenes and Analogous Higher Cumulenes
32.2 Product Class 2: Monofunctionalized Allenes and Higher Cumulenes
32.3 Product Class 3: 1,2-Bis(heteroatom-substituted) Alkenes
32.3.1 Product Subclass 1: 1,2-Dihaloalkenes
32.3.2 Product Subclass 2: 1-Halo-2-(organooxy)alkenes
32.3.3 Product Subclass 3: 1-Halo-2-(organochalcogeno)alkenes
32.3.4 Product Subclass 4: 1-Nitrogen-Functionalized 2-Haloalkenes
32.3.5 Product Subclass 5: 1-Phosphorus-Functionalized 2-Haloalkenes
32.3.6 Product Subclass 6: 1,2-Bis(organooxy)alkenes
32.3.7 Product Subclass 7: 1-(Organochalcogeno)-2-(organooxy)alkenes
32.3.8 Product Subclass 8: 1-Nitrogen-Functionalized 2-(Organooxy)alkenes
32.3.9 Product Subclass 9: 1-Phosphorus-Functionalized 2-(Organooxy)alkenes
32.3.10 Product Subclass 10: 1,2-Bis(sulfur-functionalized) Alkenes
32.3.11 Product Subclass 11: 1-Sulfur-Functionalized 2-(Organochalcogeno)-alkenes
32.3.12 Product Subclass 12: 1-Sulfur-Functionalized 2-Nitrogen-Functionalized Alkenes
32.3.13 Product Subclass 13: 1-Sulfur-Functionalized 2-Phosphorus-Functionalized Alkenes
32.3.14 Product Subclass 14: 1,2-Bis(nitrogen-functionalized) Alkenes
32.3.15 Product Subclass 15: 1-Nitrogen-Functionalized 2-Phosphorus-Functionalized Alkenes
32.3.16 Product Subclass 16: 1,2-Bis(phosphorus-functionalized) Alkenes
32.4 Product Class 4: Haloalkenes
32.5 Product Class 5: (Organooxy)alkenes
32.5.1 Product Subclass 1: Enols
32.5.2 Product Subclass 2: Enolates
32.5.3 Product Subclass 3: Enol Ethers
32.5.4 Product Subclass 4: Ene-OX Compounds (X = O, S, Se, Te)
32.5.5 Product Subclass 5: Ene-ON Compounds
32.5.6 Product Subclass 6: Ene-OP Compounds