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Houben–Weyl

 

Volume 5

The table of contents and authors for Volume 5 are given in the table below.

TABLE OF CONTENTSAUTHOR
IntroductionThomas and Moloney
5.1Germanium CompoundsThomas
5.1.1Germanium HydridesOshima
5.1.2Digermenes and DigermanesTakeda/Tokitoh/Okazaki
5.1.3Metalated Germanium CompoundsTakeda/Tokitoh/Okazaki
5.1.4Germanium Oxides, Sulfides, Selenides, and Tellurides (Double Bonded)Takeda/Tokitoh/Okazaki
5.1.5IminogermanesTakeda/Tokitoh/Okazaki
5.1.6GermenesTakeda/Tokitoh/Okazaki
5.1.7GermylenesTakeda/Tokitoh/Okazaki
5.1.8Organogermanium HalidesTakeda/Tokitoh/Okazaki
5.1.9Germanium OxidesThornton
5.1.10Germanium Carboxylates, Phosphates, and Related CompoundsThornton
5.1.11Germanium Sulfides, Sulfoxides, and Related CompoundsThornton
5.1.12Germanium Selenides, Tellurides, and Related CompoundsThornton
5.1.13GermylaminesThornton
5.1.14Germanium Phosphines, Arsines, and StibinesThornton
5.1.15Germanium CyanidesSpivey/Diaper
5.1.16AcylgermanesSpivey/Diaper
5.1.17Imidoylgermanes (a-Iminoalkylgermanes) and a-DiazoalkylgermanesSpivey/Diaper
5.1.18a-Halo- and a-AlkoxyvinylgermanesSpivey/Diaper
5.1.19a-Halo, a-Hydroxy-, a-Alkoxy-, and -AminoalkylgermanesSpivey/Diaper
5.1.20AlkynylgermanesSpivey/Diaper
5.1.21Germylketenes and GermylketeniminesSpivey/Diaper
5.1.22Aryl- and HeteroarylgermanesSpivey/Diaper
5.1.23VinylgermanesSpivey/Diaper
5.1.24Propargyl- and AllenylgermanesSpivey/Diaper
5.1.25BenzylgermanesSpivey/Diaper
5.1.26AllylgermanesSpivey/Diaper
5.1.27AlkylgermanesSpivey/Diaper
5.2Tin CompoundsThomas
5.2.1Tin HydridesClark
5.2.2Distannenes and DistannanesPodlech
5.2.3Metalated Tin CompoundsPodlech
5.2.4Tin Oxides, Sulfides, Selenides, and Tellurides (Double Bonded)Takeda/Tokitoh/Okazaki
5.2.5IminostannanesTakeda/Tokitoh/Okazaki
5.2.6StannenesTakeda/Tokitoh/Okazaki
5.2.7StannylenesTakeda/Tokitoh/Okazaki
5.2.8Tin Halides and Organotin HalidesWood
5.2.9Tin OxidesJousseaume
5.2.10Tin Carboxylates and PhosphatesJousseaume
5.2.11Tin Enol EthersJousseaume
5.2.12Tin Sulfides, Thioalkoxides, and Related CompoundsJousseaume
5.2.13Tin Selenides and TelluridesJousseaume
5.2.14Organostannylamines and Related CompoundsJousseaume
5.2.15OrganostannylphosphinesJousseaume
5.2.16Tin Cyanides and FulminatesWyatt
5.2.17Acylstannanes (Including S, Se, and Te Analogues)Wyatt
5.2.18Imidoylstannanes, Diazoalkylstannanes, Tin Isocyanates, and Tin IsothiocyanatesWyatt
5.2.191-Halo-, 1-Alkoxy-, and 1-AminovinylstannanesColdham/Vennall
5.2.201-Halo-, 1-Hydroxy-, 1-Alkoxy-, and 1-AminoalkylstannanesColdham/Vennall
5.2.21AlkynylstannanesCrisp
5.2.22Ketenylstannanes and DerivativesCrisp
5.2.23AllenylstannanesCrisp
5.2.24ArylstannanesCrisp
5.2.25Alk-1-enylstannanesCrisp
5.2.26PropargylstannanesYoung
5.2.27BenzylstannanesMarshall
5.2.28AllylstannanesMarshall
5.2.29AlkylstannanesYoung
5.3Lead CompoundsMoloney
5.3.1Lead HydridesMoloney
5.3.2Diplumbenes and DiplumbanesTakeda/Tokitoh/Okazaki
5.3.3Metalated Lead CompoundsTakeda/Tokitoh/Okazaki
5.3.4Organoplumbyl Oxides, Sulfides, Selenides, and Tellurides (Double Bonded)Takeda/Tokitoh/Okazaki
5.3.5PlumbylenesTakeda/Tokitoh/Okazaki
5.3.6Halo(organo)plumbanesGuiry/McCormack
5.3.7Organoplumboxanes and Related CompoundsGuiry/McCormack
5.3.8Acyloxy(organo)plumbanesGuiry/McCormack
5.3.9Plumbyl Enol EthersGuiry/McCormack
5.3.10Organoplumbane Sulfur CompoundsGuiry/McCormack
5.3.11Organoplumbyl Selenides, Tellurides, and Related CompoundsGuiry/McCormack
5.3.12Organoplumbanamines and Related CompoundsGuiry/McCormack
5.3.13Organoplumbyl Phosphines and Phosphine OxidesGuiry/McCormack
5.3.14Triorganolead Cyanides and Triorganolead CyanatesEagle
5.3.15AcylplumbanesEagle
5.3.16Lead Isocyanates, Isothiocyanates, Diazoplumbanes, and IminoplumbanesEagle
5.3.171- or 2-Alkoxy- and 1- or 2-(Alkylsulfanyl) and 1- or 2-Aminoalkenyl(triorgano)plumbanesEagle
5.3.181-Halo, 1-Alkoxy-, 1-Hydroxy, and 1-AminoalkylplumbanesEagle
5.3.19AlkynylplumbanesEagle
5.3.20AllenylplumbanesEagle
5.3.21ArylplumbanesEagle
5.3.22VinylplumbanesEagle
5.3.23BenzylplumbanesEagle
5.3.24AllylplumbanesEagle
5.3.25AlkylplumbanesEagle
 

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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