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Houben–Weyl

 

Volume 31a

The table of contents and authors for Volume 31a are given below.

TABLE OF CONTENTSAUTHOR
IntroductionC. A. Ramsden
31.1Product Class 1:
Fluoroarenes
G. Sandford
31.2Product Class 2:
Chloroarenes
S. P. Stanforth
31.3Product Class 3:
Bromoarenes
S. P. Stanforth
31.4Product Class 4:
Hypervalent Iodoarenes and Aryliodonium Salts
V. V. Zhdankin
31.4.1Product Subclass 1:
Alk-1-enesulfinic Acids and Derivatives
J. C. Carretero
R. G. Arrayás
31.4.2Product Subclass 2:
Iodoarenes
S. R. Waldvogel
K. M. Wehming
31.5Product Class 5:
Phenols and Phenolates
 
31.5.1Product Subclass 1:
Monohydric Phenols and Corresponding Phenolates
C. González-Bello
L. Castedo
31.5.1.1Synthesis by SubstitutionC. González-Bello
L. Castedo
31.5.1.2Synthesis by EliminationC. González-Bello
L. Castedo
31.5.1.3Synthesis by RearrangementC. González-Bello
L. Castedo
31.5.1.4Synthesis with Retention of the Functional GroupC. González-Bello
L. Castedo
31.5.1.5Synthesis from Nonaromatic PrecursorsA. W. Thomas
31.5.2Product Subclass 2:
Polyhydric Phenols and Corresponding Phenolates
M. A. Marsini
T. R. R. Pettus
31.5.2.1Synthesis by SubstitutionM. A. Marsini
T. R. R. Pettus
31.5.2.2Synthesis by EliminationM. A. Marsini
T. R. R. Pettus
31.5.2.3Synthesis by AdditionM. A. Marsini
T. R. R. Pettus
31.5.2.4Synthesis by RearrangementD. Avilov
M. A. Marsini
T. R. R. Pettus
31.5.2.5Synthesis with Retention of the Functional GroupM. A. Marsini
T. R. R. Pettus
31.6Product Class 6:
Aryl Ethers
 
31.6.1Product Subclass 1:
Diaryl Ethers
A. W. Thomas
31.6.2Product Subclass 2:
Alkyl Aryl Ethers
C. M. R.Low
31.6.2.1Synthesis by SubstitutionC. M. R.Low
31.6.2.2Synthesis by EliminationC. M. R.Low
31.6.2.3Synthesis by RearrangementC. M. R.Low
31.6.2.4Synthesis with Retention of the Functional GroupC. M. R.Low
31.6.2.5Synthesis from Nonaromatic PrecursorsM. Gerster
A. W. Thomas
31.7Product Class 7:
Aryl Hypohalites, Aryl Peroxides, and Aryloxy Sulfur Compounds
J. Chen
C. K.-F. Chiu
31.8Product Class 8:
CyclicArylEthers
D. Craig
31.9Product Class 9:
Arenesulfonic Acids and Derivatives
 
31.9.1Product Subclass 1:
Arenesulfonic Acids and Arenesulfonate Salts
B. Fravel
R. Murugan
E. F. V. Scriven
31.9.2Product Subclass 2:
Arenesulfonic Acid Derivatives
I. Shcherbakova
31.10Product Class 10:
Aryl Sulfones and Nitrogen Derivativess
S. Nakamura
T. Toru
31.11Product Class 11:
Arenesulfinic Acids and Derivatives
S. Nakamura
T. Toru
31.12Product Class 12:
Aryl Sulfoxides and S-Arylsulfimides
S. G. Collins
A. R. Maguire
31.13Product Class 13:
Arenethiols and Arenethiolates
O. A. Rakitin
31.14Product Class 14:
Aryl Sulfides
O. A. Rakitin
31.15Product Class 15:
Arylsulfonium Salts and Derivatives
I. Fernnádez
N. Khiar
31.16Product Class 16:
Arenesulfenic Acids and Derivatives
S. Perrio
V. Reboul
P. Metzner
31.17Product Class 17:
Aryl Polysulfides
O. A. Rakitin
31.18Product Class 18:
Cyclic Aryl Sulfides
O. A. Rakitin
31.19Product Class 19:
Aryl Selenium Compounds
S. Watanabe
T. Kataoka
31.20Product Class 20:
Aryl Tellurium Compounds
T. Kataoka
S. Watanabe
 

News

Award for
Eric N. Jacobsen

We would like to congratulate Eric N. Jacobsen, Editorial Board Member, Science of Synthesis, on being awarded the Yamada–Koga Prize 2008 which is awarded every year to a scientist whose research has a major impact in the fields of the synthesis of optically active compounds. The Yamada–Koga Prize will be awarded to Professor Eric N. Jacobsen on November 14, 2008, at the 18th Symposium on Optically Active Compounds held in Tokyo, Japan.

Awards for
Steven V. Ley

We would like to congratulate Steven V. Ley, Editorial Board Member, Science of Synthesis, on receiving the Prous Institute-Overton and Meyer Award for New Technologies in Drug Discovery, European Federation of Medicinal Chemistry, Vienna (2008) and the Hans Heroff Inhoffen Medal, Helmholtz Zentrum für Infectionsforschung (2008).

Professor
John Colin Tatlow
(1923–2008)

We are very sorry to announce that Professor John Colin Tatlow passed away in the UK on April 9th, 2008. Professor Tatlow was the Editor-in-Chief of the E10 Organo-Fluorine Compounds (Houben–Weyl) series and made a major contribution to fluorine chemistry during his career. He was the recipient of the American Chemical Society Award for Creative Work in Fluorine Chemistry in 1990. We would like to extend our sincere condolences to his family and friends.

Over 18,000
New Reactions
Added to

Science of Synthesis
Version 3.5
New York/Stuttgart – Thieme is pleased to announce that Science of Synthesis Version 3.5 is now available. The electronic information resource now contains 34 volumes, out of what will eventually be a total of 48 volumes. This upgraded version has a total of 195,000 reactions, with over 18,000 new reactions, and holds significant synthetic methods for a wide range of classes of compounds. The newly added content consists of volumes 29 and 31

Volume Publication

Science of Synthesis
Volume 37
We are very pleased to announce the publication of Science of Synthesis Volume 37 [Compounds with One Saturated Carbon¾Heteroatom Bond: Ethers] by Craig J. Forsyth and Eric N. Jacobsen in May 2008. The volume is 992 pages in length and provides a critical review of methods for the synthesis of ethers.

Thieme IUPAC Prize

Congratulations to
F. Dean Toste,
recipient of the 2008 Thieme–IUPAC Prize.

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