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Houben–Weyl

 

Volume 24

The table of contents and authors for Volume 24 are given below.

TABLE OF CONTENTSAUTHOR
IntroductionA. de Meijere
24.1.11,1-DihaloallenesR. R. Kostikov
24.1.21-Halo-1-(organooxy)allenesR. Zimmer
24.1.31-Halo-1-(organochalcogeno)allenes and 1-Halo-1-(organochalcogeno)butatrienesR. Zimmer
24.1.41-Nitrogen-Functionalized 1-HaloallenesR. Zimmer
24.1.51-Phosphorus-Functionalized 1-HaloallenesR. Zimmer
24.1.61,1-Bis(organooxy)allenes, 1,1-Bis(organooxy)butatrienes, 1-(Organooxy)-1-siloxyallenes, and 1-(Organooxy)allen-1-olatesR. Zimmer
24.1.71-(Organochalcogeno)-1-(organooxy)allenesR. Zimmer
24.1.81-Nitrogen-Functionalized 1-(Organooxy)allenes and Allen-1-olatesR. Zimmer
24.1.91-Phosphorus-Functionalized 1-(Organooxy)allenes and 1-SiloxyallenesR. Zimmer
24.1.101,1-Bis(organochalcogeno)allenes and 1,1-Bis(organochalcogeno)butatrienesR. Zimmer
24.1.111-Nitrogen-Functionalized 1-(Organochalcogeno)allenesR. Zimmer
24.1.121-Phosphorus-Functionalized 1-(Organochalcogeno)allenesR. Zimmer
24.1.131,1-Bis(nitrogen-functionalized) Allenes and ButatrienesR. Zimmer
24.1.141-Nitrogen-Functionalized 1-Phosphorus-Functionalized AllenesR. Zimmer
24.1.151,1-Bis(phosphorus-functionalized) AllenesM. Stankevic/
K. M. Pietrusiewicz
24.2.11,1-Dihaloalk-1-enesR. R. Kostikov
24.2.21-Halo-1(organooxy)alk-1-enesA. P. Molchanov/
R. R. Kostikov
24.2.31-Halo-1-(organochalcogeno)alk-1-enesA. F. Khlebnikov/
R. R. Kostikov
24.2.41-Nitrogen-Functionalized 1-Haloalk-1-enesJ. G. Schantl
24.2.51-Phosphorus-Functionalized 1-Haloalk-1-enesM. Stankevic/
K. M. Pietrusiewicz
24.2.61,1-Bis(organooxy)alk-1-enesC. Schneider
24.2.71-(Organooxy)-1-(organosulfanyl)alk-1-enesW. Dölling
24.2.81-(Organooxy)-1-(organoselanyl)- and 1-(Organooxy)-1-(organotellanyl)alk-1-enesW. Dölling
24.2.91-Nitrogen-Functionalized 1-(Organooxy)alk-1-enes (Ketene O,N-Acetals)W. Kantlehner
24.2.101-Phosphorus-Functionalized 1-(Organooxy)alk-1-enesH. Heydt
24.2.111,1-Bis(organosulfanyl)alk-1-enes (Ketene S,S-Acetals)W. Dölling
24.2.121-(Organoselanyl)-1-(organosulfanyl)alk-1-enes and 1-(Organosulfanyl)-1-(organotellanyl)alk-1-enesM. Yoshimatsu
24.2.131-Nitrogen-Functionalized 1-(Organosulfanyl)alk-1-enesW. Dölling
24.2.141-Phosphorus-Functionalized 1-(Oragnosulfanyl)alk-1-enesJ. Romanski/
G. Mloston/
K. M. Pietrusiewicz
24.2.151,1-Bis(organoselanyl)alk-1-enes and DerivativesM. Yoshimatsu
24.2.161,1-Bis(organotellanyl)alk-1-enes and DerivativesM. Yoshimatsu
24.2.17.1Alk-1-ene-1,1-diaminesW. Kantlehner
24.2.17.2Alk-1-ene-1,1-diamines with Retention of the Functional GroupP. A. Keller/
J. Morgan
24.2.17.31,1-Bisazo-, 1,1-Diazido-, and 1,1-Dinitroalk-1-enesK. Banert
24.2.181-Nitrogen-Functionalized 1-Phosphorus-Functionalized Alk-1-enesM. Stankevic and K. M. Pietrusiewicz
24.2.191,1-Bis(phosphorus-functionalized) Alk-1-enesM. Stankevic and K. M. Pietrusiewicz
24.3.1DihaloacetylenesB. Witulski/
C. Alayrac
24.3.21-Heteroatom-Functionalized 2-HaloacetylenesB. Witulski/
C. Alayrac
24.3.3Bis(organooxy)acetylenesB. Witulski/
C. Alayrac
24.3.41-(Organochalcogeno)-2-(organooxy)acetylenesB. Witulski/
C. Alayrac
24.3.51-Nitrogen-Functionalized 2-(Organooxy)acetylenesB. Witulski/
C. Alayrac
24.3.61-Phophorus-Functionalized 2-(Organooxy)acetylenesB. Witulski/
C. Alayrac
24.3.7Bis(organochalcogeno)acetylenesT. Murai
24.3.81-Nitrogen-Functionalized 2-(Organochalcogeno)acetylenesT. Murai
24.3.92-Phosphorus-Functionalized 1-(Organochalcogeno)acetylenesT. Murai
24.3.10Bis(nitrogen-functionalized) AcetylenesB. Witulski/
C. Alayrac
24.3.111-Nitrogen-Functionalized 2-Phosphorus-Functionalized Acetylenes and Bis(phosphorus-functionalized) AcetylenesB. Witulski/
C. Alayrac
24.4.11-Haloalk-1-ynes and Alk-1-yn-1-olsB. Witulski/
C. Alayrac
24.4.21-(Organooxy)alk-1-ynes and 1-(Heterooxy)alk-1-ynesB. Witulski/
C. Alayrac
24.4.31-(Organosulfanyl)-, 1-(Organoselanyl)-, and 1-(Organotellanyl)alk-1-ynesV. A. Potapov/
B. A. Trofimov
24.4.4.1Alk-1-yn-1-aminesB. Witulski/
C. Alayrac
24.4.4.2N-Acyl- and N-Sulfonylalk-1-yn-1-aminesB. Witulski/
C. Alayrac
24.4.4.3Alk-1-ynyldiazonium Salts, 1-Azidoalk-1-ynes, and 1-Nitroalk-1-ynesK. Banert
24.4.51-Phosphorus-Functionalized Alk-1-ynesK. M. Pietrusiewicz/
M. Stankevic
 

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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