Thieme Chemistry - Science of Synthesis


	Home Journals	Reference Works	Encyclopedias	Monographs

Project Information

Order Information

Order Online

Volume Information

Volumes

	Category 1
	Category 2
	Category 3
	Category 4
	Category 5
	Category 6

For Authors

Contacts

Volume 35

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

TABLE OF CONTENTS		AUTHOR
	Introduction	E. Schaumann
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

Thieme Chemistry beta website

Try out our new beta website.

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.