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Volume 39

The table of contents and authors for Volume 35 are given below.

TABLE OF CONTENTS		AUTHOR
	Introduction	N. Kambe
35.1	Product Class 1: One Saturated Carbon¾Chlorine Bond
35.1.1	Product Subclass 1: Chloroalkanes	E. Schaumann
35.1.1.1	Synthesis by Substitution of Hydrogen	J. Hartung
35.1.1.2	Synthesis by Substitution of Metals	P. Margaretha
35.1.1.3	Synthesis by Substitution of Carbon Functionalities	P. Margaretha
35.1.1.4	Synthesis by Substitution of Other Halogens	P. Margaretha
35.1.1.5	Synthesis by Substitution of Oxygen Functionalities	P. Margaretha
35.1.1.6	Synthesis by Substitution of Sulfur, Selenium, or Tellurium Functionalities	P. Margaretha
35.1.1.7	Synthesis by Substitution of Nitrogen Functionalities	P. Margaretha
35.1.1.8	Synthesis by Addition to π-Type C¾C Bonds	K.-M. Roy
35.1.1.9	Synthesis from Other Chlorine Compounds	H. Ulrich
35.1.2	Product Subclass 2: Propargylic Chlorides	P. Margaretha
35.1.3	Product Subclass 3: Benzylic Chlorides
35.1.3.1	Synthesis by Substitution of Hydrogen	W. D. Pfeiffer
35.1.3.2	Synthesis by ubstitution of Carbonyl Oxygen	W. D. Pfeiffer
35.1.3.3	Synthesis by Substitution of σ-Bonded Heteroatoms	P. Margaretha
35.1.4	Product Subclass 4: Allylic Chlorides
35.1.4.1	Synthesis by Substitution of Hydrogen α to a C=C Bond	W. D. Pfeiffer
35.1.4.2	Synthesis by Substitution of σ-Bonded Heteroatoms	P. Margaretha
35.1.5	Product Subclass 5: 1-Chloro-n-Heteroatom-Functionalized Alkanes (n≥2) with Both Functions Formed Simultaneously
35.1.5.1	Synthesis by Addition across C=C Bonds	R. Göttlich
35.1.5.2	Synthesis by Addition across C¾O Bonds	K. Rück-Braun T. Freysoldt
35.1.5.3	Synthesis by Addition across C¾S Bonds	R. Göttlich
35.1.5.4	Synthesis by Addition across C¾N Bonds	K. Rück-Braun T. Freysoldt
35.1.5.5	Synthesis by Addition across C¾C Bonds	K. Rück-Braun T. Freysoldt
35.2	Product Class 2: One Saturated Carbon¾Bromine Bond
35.2.1	Product Subclass 1: Bromoalkanes	E. Schaumann
35.2.1.1	Synthesis by Substitution of Hydrogen	J. Hartung
35.2.1.2	Synthesis by Substitution of Metals	P. Margaretha
35.2.1.3	Substitution of Carbon Functionalities	P. Margaretha
35.2.1.4	Synthesis by Substitution of Other Halogens	M. Braun
35.2.1.5	Synthesis by Substitution of Oxygen Functionalities	M. Braun
35.2.1.6	Synthesis by Substitution of Sulfur, Selenium, or Tellurium Functionalities	M. Braun
35.2.1.7	Synthesis by Substitution of Nitrogen Functionalities	M. Braun
35.2.1.8	Synthesis by Addition to π-Type C¾C Bonds	K.-M. Roy
35.2.1.9	Synthesis from Other Bromo Compounds	H. Ulrich
35.2.2	Product Subclass 2: Propargylic Bromides	M. Braun
35.2.3	Product Subclass 3: Benzylic Bromides
35.2.3.1	Synthesis by Substitution of Hydrogen	W. D. Pfeiffer
35.2.3.2	Synthesis by Substitution of Carbonyl Oxygen	W. D. Pfeiffer
35.2.3.3	Synthesis by Substitution of σ-BondedHeteroatoms	W. D. Pfeiffer
35.2.4	Product Subclass 4: Allylic Bromides
35.2.4.1	Synthesis by Substitution of Hydrogen α to a C=C Bond	W. D. Pfeiffer
35.2.4.2	Synthesis by Substitution of α-Bonded Heteroatoms	M. Braun
35.2.5	Product Subclass 5: 1-Bromo-n-Heteroatom-Functionalized Alkanes (n≥2) with Both Functions Formed Simultaneously
35.2.5.1	Synthesis by Addition across C=C Bonds	T. Troll
35.2.5.2	Synthesis by Addition across C¾O Bonds	K. Rück-Braun T. Freysoldt
35.2.5.3	Synthesis by Addition across C¾S Bonds	K. Rück-Braun T. Freysoldt
35.2.5.4	Synthesis by Addition across C¾N Bonds	K. Rück-Braun T. Freysoldt
35.2.5.5	Synthesis by Addition across C¾C Bonds	K. Rück-Braun T. Freysoldt
35.3	Product Class 3: One Saturated Carbon¾Iodine Bond
35.3.1	Product Subclass 1: Iodoalkanes	E. Schaumann
35.3.1.1	Synthesis by Substitution of Hydrogen	J. Hartung
35.3.1.2	Synthesis by Substitution of Metals	S. Härtinger M. Härtinger
35.3.1.3	Synthesis by Substitution of Carbon Functionalities	S. Härtinger M. Härtinger
35.3.1.4	Synthesis by Substitution of Other Halogens	S. Härtinger M. Härtinger
35.3.1.5	Synthesis by Substitution of Oxygen Functionalities	S. Härtinger
35.3.1.6	Synthesis by Substitution of Sulfur, Selenium, or Tellurium Functionalities	S. Härtinger M. Härtinger
35.3.1.7	Synthesis by Substitution of Nitrogen Functionalities	S. Härtinger M. Härtinger
35.3.1.8	Synthesis by Addition to π-Type C¾C Bonds	S. Härtinger M. Härtinger
35.3.1.9	Synthesis from Other Iodo Compounds	H. Ulrich
35.3.2	Product Subclass 2: Propargylic Iodides	S. Härtinger
35.3.3	Product Subclass 3: Benzylic Iodides
35.3.3.1	Synthesis by Substitution of Carbonyl Oxygen	W. D. Pfeiffer
35.3.3.2	Substitution of σ-Bonded Heteroatoms	S. Härtinger M. Härtinger
35.3.4	Product Subclass 4: Allylic Iodides	S. Härtinger
35.3.5	Product Subclass 5: 1-Iodo-n-Heteroatom-Functionalized Alkanes (n≥2) with Both Functions Formed Simultaneously
35.3.5.1	Synthesis by Addition across C=C Bonds	T. Troll
35.3.5.2	Synthesis by Addition across C¾O Bonds	K.Rück-Braun T. Freysoldt
35.3.5.3	Synthesis by Addition across C¾S Bonds	K.Rück-Braun T. Freysoldt
35.3.5.4	Synthesis by Addition across C¾N Bonds	K.Rück-Braun T. Freysoldt
35.3.5.5	Synthesis by Addition across C¾C Bonds	K.Rück-Braun T. Freysoldt

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.