Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol. 35

Ernst Schaumann

Ernst Schaumann
Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol. 35 [EPUB ebook]
Chlorine, Bromine, and Iodine

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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 an...

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35.1 Product Class 1: One Saturated Carbon—Chlorine Bond 35.1.1 Product Subclass 1: Chloroalkanes 35.1.1.1 Synthesis by Sub...

Innehållsförteckning

35.1 Product Class 1: One Saturated Carbon—Chlorine Bond 35.1.1 Product Subclass 1: Chloroalkanes 35.1.1.1 Synthesis by Substitution of Hydrogen 35.1.1.2 Synthesis by Substitution of Metals 35.1.1.3 Synthesis by Substitution of Carbon Functionalities 35.1.1.4 Synthesis by Substitution of Other Halogens 35.1.1.5 Synthesis by Substitution of Oxygen Functionalities 35.1.1.6 Synthesis by Substitution of Sulfur, Selenium, or Tellurium Functionalities 35.1.1.7 Synthesis by Substitution of Nitrogen Functionalities 35.1.1.8 Synthesis by Addition to π-Type C—C Bonds 35.1.1.9 Synthesis from Other Chlorine Compounds 35.1.2 Product Subclass 2: Propargylic Chlorides 35.1.3 Product Subclass 3: Benzylic Chlorides 35.1.3.1 Synthesis by Substitution of Hydrogen 35.1.3.2 Synthesis by Substitution of Carbonyl Oxygen 35.1.3.3 Synthesis by Substitution of σ-Bonded Heteroatoms 35.1.4 Product Subclass 4: Allylic Chlorides 35.1.4.1 Synthesis by Substitution of Hydrogen α to a C=C Bond 35.1.4.2 Synthesis by Substitution of σ-Bonded Heteroatoms 35.1.5 Product Subclass 5: 1-Chloro-n-Heteroatom-Functionalized Alkanes (n ≥2) with Both Functions Formed Simultaneously 35.1.5.1 Synthesis by Addition across C=C Bonds 35.1.5.2 Synthesis by Addition across C—O Bonds 35.1.5.3 Synthesis by Addition across C—S Bonds 35.1.5.4 Synthesis by Addition across C—N Bonds 35.1.5.5 Synthesis by Addition across C—C Bonds 35.2 Product Class 2: One Saturated Carbon—Bromine Bond 35.2.1 Product Subclass 1: Bromoalkanes 35.2.1.1 Synthesis by Substitution of Hydrogen 35.2.1.2 Synthesis by Substitution of Metals 35.2.1.3 Substitution of Carbon Functionalities 35.2.1.4 Synthesis by Substitution of Other Halogens 35.2.1.5 Synthesis by Substitution of Oxygen Functionalities 35.2.1.6 Synthesis by Substitution of Sulfur, Selenium, or Tellurium Functionalities 35.2.1.7 Synthesis by Substitution of Nitrogen Functionalities 35.2.1.8 Synthesis by Addition to π-Type C—C Bonds 35.2.1.9 Synthesis from Other Bromo Compounds 35.2.2 Product Subclass 2: Propargylic Bromides 35.2.3 Product Subclass 3: Benzylic Bromides 35.2.3.1 Synthesis by Substitution of Hydrogen 35.2.3.2 Synthesis by Substitution of Carbonyl Oxygen 35.2.3.3 Synthesis by Substitution of σ-Bonded Heteroatoms 35.2.4 Product Subclass 4: Allylic Bromides 35.2.4.1 Synthesis by Substitution of Hydrogen α to a C=C Bond 35.2.4.2 Synthesis by Substitution of σ-Bonded Heteroatoms 35.2.5 Product Subclass 5: 1-Bromo-n-Heteroatom-Functionalized Alkanes (n ≥2) with Both Functions Formed Simultaneously 35.2.5.1 Synthesis by Addition across C=C Bonds 35.2.5.2 Synthesis by Addition across C—O Bonds 35.2.5.3 Synthesis by Addition across C—S Bonds 35.2.5.4 Synthesis by Addition across C—N Bonds 35.2.5.5 Synthesis by Addition across C—C Bonds 35.3 Product Class 3: One Saturated Carbon—Iodine Bond 35.3.1 Product Subclass 1: Iodoalkanes 35.3.1.1 Synthesis by Substitution of Hydrogen 35.3.1.2 Synthesis by Substitution of Metals 35.3.1.3 Synthesis by Substitution of Carbon Functionalities 35.3.1.4 Synthesis by Substitution of Other Halogens 35.3.1.5 Synthesis by Substitution of Oxygen Functionalities 35.3.1.6 Synthesis by Substitution of Sulfur, Selenium, or Tellurium Functionalities 35.3.1.7 Synthesis by Substitution of Nitrogen Functionalities 35.3.1.8 Synthesis by Addition to π-Type C—C Bonds 35.3.1.9 Synthesis from Other Iodo Compounds 35.3.2 Product Subclass 2: Propargylic Iodides 35.3.3 Product Subclass 3: Benzylic Iodides 35.3.3.1 Synthesis by Substitution of Carbonyl Oxygen 35.3.3.2 Substitution of σ-Bonded Heteroatoms 35.3.4 Product Subclass 4: Allylic Iodides 35.3.5 Product Subclass 5: 1-Iodo-n-Heteroatom-Functionalized Alkanes (n ≥2) with Both Functions Formed Simultaneously 35.3.5.1 Synthesis by Addition across C=C Bonds 35.3.5.2 Synthesis by Addition across C—O Bonds 35.3.5.3 Synthesis by Addition across C—S Bonds 35.3.5.4 Synthesis by Addition across C—N Bonds 35.3.5.5 Synthesis by Addition across C—C Bonds

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Språk Engelska ● Formatera EPUB ● Sidor 850 ● ISBN 9783131783110 ● Filstorlek 27.2 MB ● Redaktör Ernst Schaumann ● Utgivare Thieme ● Stad Stuttgart ● Land DE ● Publicerad 2014 ● Utgåva 1 ● Nedladdningsbara 24 månader ● Valuta EUR ● ID 3140715 ● Kopieringsskydd Social DRM