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

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Over 20,000
New Reactions

Science of Synthesis 3.6 is now available and contains 38 volumes with a total of 215,000 reactions. More details on the newly released version 3.6.

Award for
Barry M. Trost

We would like to congratulate Barry M. Trost, Editorial Board Member, Science of Synthesis, on being awarded the Nagoya Gold Medal of Organic Chemistry 2008.

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 will be awarded 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 and the Hans Herloff Inhoffen Medal.

Volume Publication

We are pleased to announce the publication of Science of Synthesis Volume 37 [Ethers] by Craig J. Forsyth and Eric N. Jacobsen in May 2008.

Professor
John Colin Tatlow
(1923–2008)

We are very sorry to announce that Professor John Colin Tatlow passed away 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.

Thieme IUPAC Prize

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