Thieme Chemistry - Science of Synthesis


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Volume 33

The table of contents and authors for Volume 33 are given below.

TABLE OF CONTENTS		AUTHOR
	Introduction	G. A. Molander
33.1	Product Class 1: Alk-1-enyl Sulfur Compounds
33.1.1	Product Subclass 1: Alk-1-enesulfonic Acids and Derivatives	J. C. Carretero R. G. Arrayás
33.1.2	Product Subclass 2: Alk-1-enyl Sulfones	J. C. Carretero R. G. Arrayás
33.1.3	Product Subclass 3: S-Alk-1-enylsulfoximides	J. C. Carretero R. G. Arrayás
33.1.4	Product Subclass 4: Alk-1-enesulfinic Acids and Derivatives	J. C. Carretero R. G. Arrayás
33.1.5	Product Subclass 5: Alk-1-enyl Sulfoxides, Sulfimides, and Related Compounds	J. C. Carretero R. G. Arrayás
33.1.6	Product Subclass 6: Alk-1-enethiols	J. Drabowicz P.Kiełbasiński M.Mikołajczyk
33.1.7	Product Subclass 7: Metal Alk-1-enethiolates	J. Drabowicz P.Kiełbasiński M.Mikołajczyk
33.1.8	Product Subclass 8: Alk-1-enyl Sulfides	J. Drabowicz P.Kiełbasińskik M.Mikołajczyk
33.1.9	Product Subclass 9: Alk-1-enyl sulfonium Salts	J. Drabowicz P.Kiełbasińskik M.Mikołajczyk
33.1.10	Product Subclass 10: Alk-1-enesulfenic Acid Derivatives	J. Drabowicz P.Kiełbasińskik M.Mikołajczyk
33.1.11	Product Subclass 11: Alk-1-enyl Disulfides	J. Drabowicz P.Kiełbasińskik M.Mikołajczyk
33.1.12	Product Subclass 12: Thietes and Derivatives	E. Block
33.1.13	Product Subclass 13: 2,3-Dihydrothiophenes and Derivatives	E. Block
33.1.14	Product Subclass 14: 3,4-Dihydro-2H-thiopyrans and Derivatives	E. Block
33.1.15	Product Subclass 15: 2,3,4,5-Tetrahydrothiepins, Larger Rings, and Derivatives	E. Block
33.2	Product Class 2: Alk-1-enyl Selenium Compounds	D. Avilov D. Dittmer
33.3	Product Class 3: Alk-1-enyl Tellurium Compounds	D. Avilov D. Dittmer
33.4	Product Class 4: Alk-1-enyl Nitrogen Compounds
33.4.1	Product Subclass 1: 1-Nitroalkenes	N. Ono
33.4.2	Product Subclass 2: 1-Nitrosoalkenes	H.-U. Reissig R. Zimmer
33.4.3	Product Subclass 3: N-Alk-1-enyliminosulfur Compounds
33.4.4	Product Subclass 4: Alk-1-enediazonium Salts, Alkeneazoxy, and Alkeneazo Compounds	H.-U. Reissig R. Zimmer
33.4.5	Product Subclass 5: N-Alk-1-enyliminophosphorus Compounds	H.-U. Reissig R. Zimmer
33.4.6	Product Subclass 6: Enamines	T. Sammakia J. A. Abramite M. F. Sammons
33.4.7	Product Subclass 7: Enammonium Salts	T. Sammakia J. A. Abramite M. F. Sammons
33.4.8	Product Subclass 8: N-Silylenamines	S. J. Collier
33.4.9	Product Subclass 9: N-Borylenamines	S. J. Collier
33.4.10	Product Subclass 10: N-Haloenamines	S. J. Collier
33.4.11	Product Subclass 11: N-Alk-1-enylhydroxylamines	S. J. Collier
33.4.12	Product Subclass 12: N-Alk-1-enylaminosulfur Compounds	S. J. Collier
33.4.13	Product Subclass 13: Alk-1-enylhydrazines	S. J. Collier M. D. McLaws
33.4.14	Product Subclass 14: Alk-1-enylAzides	S. J. Collier
33.4.15	Product Subclass 15: N-Alk-1-enylaminophosphorus Compounds	S. J. Collier
33.4.16	Product Subclass 16: 1,2-Dihydroazetes and Derivatives	P. Jubault E. Leclerc J.-C. Quirion
33.4.17	Product Subclass 17: 2,3-Dihydro-1H-pyrroles and Derivatives	P. Jubault E. Leclerc J.-C. Quirion
33.4.18	Product Subclass 18: 1,2-Dihydropyridines, 1,4-Dihydropyridines, and Derivatives	J.-C. Quirion E. Leclerc P. Jubault
33.4.19	Product Subclass 19: 1,2,3,4-Tetrahydropyridines and Derivatives	J.-C. Quirion
33.4.20	Product Subclass 20: 2,3,4,5-Tetrahydro-1H-azepines, Larger Rings, and Derivatives	J.-C. Quirion E. Leclerc P. Jubault
33.5	Product Class 5: Alk-1-enyl Phosphorus Compounds
33.5.1	Product Subclass 1: Alk-1-enylphosphonic Acids and Derivatives	A. C. Gaumont M. Gulea
33.5.2	Product Subclass 2: Alk-1-enylphosphinic Acids and Derivatives	A. C. Gaumont M. Gulea
33.5.3	Product Subclass 3: Alk-1-enylphosphine Oxides and Derivatives	A. C. Gaumont M. Gulea
33.5.4	Product Subclass 4: Alk-1-enylphosphines	A. C. Gaumont M. Gulea
33.5.5	Product Subclass 5: Alk-1-enylphosphonium Salts	A. C. Gaumont M. Gulea
33.5.6	Product Subclass 6: P-Heteroatom-Substituted Alk-1-enylphosphines	A. C. Gaumont M. Gulea
33.5.7	Product Subclass 7: 1,2-Dihydrophosphetes and Derivatives	Gy. Keglevich H. Szelke
33.5.8	Product Subclass 8: 2,3-Dihydro-1H-phospholes and Derivatives	Gy. Keglevich H. Szelke
33.5.9	Product Subclass 9: 1,2,3,4-Tetrahydrophosphinines and Derivatives	Gy. Keglevich H. Szelke
33.5.10	Product Subclass 10: 1,4-Dihydrophosphinines and Derivatives	Gy. Keglevich H. Szelke

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.