Comprehensive Organic Functional Group Transformations II, 1st Edition

  • Published By:
  • ISBN-10: 0080523471
  • ISBN-13: 9780080523477
  • DDC: 547.2
  • Grade Level Range: College Freshman - College Senior
  • 6669 Pages | eBook
  • Original Copyright 2005 | Published/Released November 2007
  • This publication's content originally published in print form: 2005

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About

Overview

This new seven-volume work builds on Elsevier's impressive and established organic chemistry MRW portfolio. Comprehensive Organic Functional Group Transformations II provides the first point of entry to the literature for all scientists interested in chemical transformations. Presenting the vast subject of organic synthesis in terms of the introduction and interconversion of all known functional groups, Comprehensive Organic Functional Group Transformations II offers a unique information source documenting all methods of efficiently performing a particular transformation.

Organized by the functional group formed, Comprehensive Organic Functional Group Transformations II consists of 144 specialist reviews, written by leading scientists who will evaluate and summarize the methods available for each functional group transformation

Table of Contents

Front Cover.
Half Title Page.
Title Page.
Copyright Page.
Contents.
Preface.
Introduction to Volume 1.
Contributors to Volume 1.
Explanation of the Reference System.
Journal Abbreviations.
1: Tetracoordinated Carbon with No Attached Heteroatoms.
2: One or More CH Bond(s) Formed by Substitution: Reduction of C—Halogen and C—Chalcogen Bonds.
3: One or More C—H Bond(s) Formed by Substitution: Reduction of Carbon—Nitrogen, —Phosphorus, —Arsenic, —Antimony, —Bismuth, —Carbon, —Boron, and —Metal Bonds.
4: Two or More CH Bond(s) Formed by Addition to CC Multiple Bonds.
5: One or More CC Bond(s) Formed by Substitution: Substitution of Halogen.
6: One or More CC Bond(s) Formed by Substitution: Substitution of Chalcogen.
7: One or More CC Bond(s) Formed by Substitution: Substitution of Carbon-Nitrogen, -Phosphorus, -Arsenic, -Antimony, -Boron, -Silicon, -Germanium, and -Metal Functions.
8: One or More CC Bonds Formed by Addition: Addition of Carbon Electrophiles and Nucleophiles to CC Multiple Bonds.
9: One or More CC Bond(s) Formed by Addition: Addition of Carbon Radicals and Electrocyclic Additions to CC Multiple Bonds.
10: One or More CH and/or CC Bond(s) Formed by Rearrangement.
11: Tricoordinated Carbon with No Attached Heteroatoms.
12: One or More =CH Bond(s) Formed by Substitution or Addition.
13: One or More =C—C Bond(s) Formed by Substitution or Addition.
14: One or More C=C Bond(s) Formed by Addition.
15: One or More C=C Bond(s) by Elimination of Hydrogen, Carbon, Halogen, or Oxygen Functions.
16: One or More C=C Bond(s) by Elimination of S, Se, Te, N, P, As, Sb, Bi, Si, Ge, B, or Metal Functions.
17: One or More C=C Bond(s) Formed by Condensation: Condensation of Nonheteroatom-linked Functions, Halides, Chalcogen, or Nitrogen Functions.
18: One or More C=C Bond(s) Formed by Condensation: Condensation of P, As, Sb, Bi, Si, Ge, B, or Metal Functions.
19: One or More C=C Bond(s) by Pericyclic Processes.
20: One or More =CH, =CC, and/or C=C Bond(s) Formed by Rearrangement.
21: Tricoordinate Carbanions, Cations, and Radicals.
22: Dicoordinate and Monocoordinate Carbon with No Attached Heteroatoms.
23: Allenes and Cumulenes.
24: Alkynes.
25: Ions, Radicals, Carbenes, and Other Monocoordinated Systems.