 |
 |
 | ANNUAL REPORTS IN ORGANIC SYNTHESIS, 2004
|  |
 |  |  |
 |
 |
To order this title, and for more information, click here
Edited By
Philip Weintraub, Hoechst Marion Roussel, Bridgewater, New Jersey, USA
Jeffrey Sabol, Aventis Pharmaceuticals, Bridgewater, New Jersey, USA
Peter Norris, Youngstown State University, Youngstown, Ohio, USA
Kenneth Turnbull, Wright State University, Department of Chemistry, Dayton, Ohio, USA
Included in series
Annual Reports in Organic Synthesis,
Description
Annual Reports in Organic Synthesis 2004 provides an organized annual review of synthetically useful information that proves beneficial
to organic chemists, both specialists and nonspecialists in synthesis.
Information appears as promptly as possible after the close
of the abstracting period and is presented in an organized manner.
Chapters I to III are organized by reaction type.
Chapter
IV deals with methods of synthesizing heterocyclic systems.
Chapter V covers the use of protecting groups.
Chapter VI deals
with those synthetically useful transformations that do not fit easily into the first three chapters.
In Chapter VII, the reviews
have been divided into sections to help the reader to quickly find a review on a specific topic.
Audience
For organic, medicinal and polymer chemists in academia and industry
Contents
CARBON–CARBON BOND FORMING REACTIONS
A. Carbon–Carbon Single Bonds.
B. Carbon–Carbon Double Bonds.
C. Carbon–Carbon Triple Bonds.
D. Cyclopropanations.
E. Thermal and Photochemical Reactions.
F. Aromatic Substitutions
Forming a New Carbon-Carbon Bond.
G. Synthesis via Organometallics.
H. Rearrangements.
OXIDATIONS
A.
C-O Oxidations.
B. C-H Oxidations.
C. C-N Oxidations.
D. Amine Oxidations.
E. Sulfur Oxidations.
F. Oxidative
Additions to C-C Multiple Bonds.
G. Phenol-Quinone Oxidation.
H. Dehydrogenation.
I. Other Oxidations.
REDUCTIONS
A. C=O Reductions.
B. C-N Multiple Bond Reductions.
C. Reduction of Sulfur Compounds.
D. N-O Reductions.
E.
C-C Multiple Bond Reductions.
F. Hetero Bond Reductions.
G. Reductive Cleavages.
H. Reduction of Azides.
I.
Other Reductions.
SYNTHESIS OF HETEROCYCLES
A. Oxiranes, Aziridines, and Thiiranes.
B. Oxetanes, Azetidines,
and Thietanes.
C. Lactams.
D. Lactones.
E. Furans and Thiophenes.
F. Pyrroles, Indoles, etc.
G. Pyridines,
Quinolines, etc.
H. Pyrans, Pyrones, and Sulfur Analogues.
I. Other Heterocycles with One Heteroatom.
J. Heterocycles
with a Bridgehead Heteroatom.
K. Heterocycles with Two or More Heteroatoms.
L. Other Heterocyles.
M. Reviews.
PROTECTING
GROUPS
A. Aldehyde and Ketone Protecting Groups.
B. Amino Acid Protection.
C. Amine Protecting Groups.
D. Carboxyl
Protecting Groups.
E. Hydroxyl Protecting Groups.
F. Other Protecting Groups.
USEFUL SYNTHETIC PREPARATIONS
A. Functional Group Preparations.
B. Additions to Alkenes and Alkynes.
C. Boron Compounds.
D. Nucleosides, Nucleotides
etc.
E. Phosphorus, Selenium and Tellurium Compounds.
F. Silicon Compounds.
G. Sulfur Compounds.
H. Tin Compounds.
REVIEWS
A. Techniques.
B. Asymmetric Synthesis and Molecular Recognition.
C. Reactions.
D. Reactive
Intermediates.
E. Organometallics and Metalloids.
F. Halogen Compounds and Halogenation.
G. Natural Products.
H. Others.
SELECTED TOPICAL AREAS
A. Fullerene Chemistry.
B. Taxol and Related Taxane Chemistry.
C. Dendrimers,
Calixarenes and Other Unnatural Products.
D. Total Syn. of Selected Natural Products.
E. Reactions in Polar Media.
F.
Combinatorial Chemistry.
| Bibliographic details |
Paperback, 440 pages, publication date: DEC-2004
ISBN-13: 978-0-12-040834-4
ISBN-10: 0-12-040834-1
Imprint: ACADEMIC PRESS
|
| Price and Ordering |
Price:
GBP 78.99 EUR 92.95 USD 130
|  |
Books and book related electronic products are priced in US dollars (USD), euro (EUR), and Great Britain Pounds (GBP). USD prices apply to the Americas and Asia Pacific. EUR prices apply in Europe and the Middle East. GBP prices apply to the UK and all other countries.
|
See also information about conditions of sale & ordering procedures, and links to our regional sales offices.
|
030/302
Last update: 30 Nov 2009
|
 |
|  |
 |  |  |
 |
|
|  |