Synthesis of Heterocycles by Metathesis Reactions
Published on 4. July 2018
Book
Paperback/Softback
XXV, 389 pages
978-3-319-82001-9 (ISBN)
Description
The series Topics in Heterocyclic Chemistry presents critical reviews on present and future trends in the research of heterocyclic compounds. Overall the scope is to cover topics dealing with all areas within heterocyclic chemistry, both experimental and theoretical, of interest to the general heterocyclic chemistry community. The series consists of topic related volumes edited by renowned editors with contributions of experts in the field. All chapters from Topics in Heterocyclic Chemistry are published Online First with an individual DOI. In references, Topics in Heterocyclic Chemistry is abbreviated as Top Heterocycl Chem and cited as a journal.
More details
Series
Edition
Softcover reprint of the original 1st ed. 2017
Language
English
Place of publication
Cham
Switzerland
Publishing group
Springer International Publishing
Target group
Professional and scholarly
Illustrations
16 s/w Abbildungen, 44 farbige Abbildungen
XXV, 389 p. 60 illus., 44 illus. in color.
Dimensions
Height: 235 mm
Width: 155 mm
Thickness: 23 mm
Weight
628 gr
ISBN-13
978-3-319-82001-9 (9783319820019)
DOI
10.1007/978-3-319-39941-6
Schweitzer Classification
Other editions
Additional editions
Joëlle Prunet
Synthesis of Heterocycles by Metathesis Reactions
Book
12/2016
Springer
€213.99
Shipment within 10-15 days
Content
Synthesis of Heteroaromatic Compounds by Alkene and Enyne Metathesis.- The Synthesis of Cyclic Ether-Containing Natural and Non-natural Products by Metathesis Reactions.- Metathetic Synthesis of Common and Medium-Sized Lactones: The State of the Art.- Synthesis of Amine-Containing Heterocycles by Metathesis Reactions: Recent Advances and Opportunities.- Synthesis of Lactams by Metathesis Reactions.- Synthesis of Cyclic Peptides and Peptidomimetics by Metathesis Reactions.- Synthesis of Macrocycles other than Peptides by Metathesis.- Synthesis of P-, S-, Si-, B-, and Se-Heterocycles via Ring-Closing Metathesis.