Cover of: Stereoselective Heterocyclic Synthesis 3 (Topics in Current Chemistry) |

Stereoselective Heterocyclic Synthesis 3 (Topics in Current Chemistry)

  • 202 Pages
  • 0.24 MB
  • 1315 Downloads

Springer
Heterocyclic compounds, Physical chemistry, Heterocyclic Chemistry, Stereochemistry, Science, Medical / Nursing, Science/Mathematics, Chemistry - Organic, General, Heterocyclen, Heterocycles, Materialwissenschaft, Medical / General, Organische Chemie, Science / Chemistry / Organic, Science-Chemistry - Organic, Stereochemie, Synthese, materials science, Chemistry - Physical & Theore
ContributionsA. Hassner (Contributor), P. ten Holte (Contributor), I.N.N. Namboothiri (Contributor), U. Nubbemeyer (Contributor), S.D. Rychnovsky (Contributor), C.J. Sinz (Contributor), B. Zwanenburg (Contributor), Peter Metz (Editor)
The Physical Object
FormatHardcover
ID Numbers
Open LibraryOL12774683M
ISBN 10354041763X
ISBN 139783540417637

Stereoselective Heterocyclic Synthesis III. Editors: Metz, Peter (Ed.) Free Preview. Buy this book eBook ,33 Stereoselective Intramolecular 1,3-Dipolar Cycloadditions. Pages Only valid for books with an ebook version.

Springer Reference Works are not included. My Account. It is the aim of this series on "Stereoselective Heterocyclic Synthesis" to assist the chemical community in this respect by presenting a selection of exciting recent developments.

As it was for the first two volumes (), the stereoselective synthesis of - or with the aid of - heterocycles is the common motif for all the chapters in this third : Paperback. This volume is part of a 3-volume set: Science of Synthesis Stereoselective Synthesis Workbench Edition Further information about Stereoselective Synthesis (including sample pages and the table of contents) About the Author.

Professor, Department of Chemistry, University of. Stereoselective Heterocyclic Synthesis III. Editors (view affiliations) Peter Metz; Book. Stereoselective Intramolecular 1,3-Dipolar Cycloadditions.

Pages 4-Acetoxy- and 4-Cyano-1,3-Dioxanes in Synthesis. Christopher J. Sinz, Scott D. Rychnovsky. Pages The Synthetic Potential of Three-Membered Ring Aza-Heterocycles.

Book: ISBN: X OCLC Number: Description: Seiten. Contents: Stereoselective Intramolecular 1,3-Dipolar Cycloadditions.- 4-Acetoxy- and 4-Cyano-1,3-Dioxanes in Synthesis.- The Synthetic Potential of Three-Membered Ring Aza-Heterocycles.- Synthesis of Medium-Sized Ring Lactams. Series Title: Topics in current chemistry,   ISBN: DOI: / Table of Contents: Stereoselective Intramolecular 1,3-Dipolar Cycloadditions.

4-Acetoxy- and 4-Cyano-1,3-Dioxanes in Synthesis. The Synthetic Potential of Three-Membered Ring Aza-Heterocycles.

Download Stereoselective Heterocyclic Synthesis 3 (Topics in Current Chemistry) EPUB

Synthesis of Medium-Sized Ring Lactams. "Stereoselective Heterocyclic Synthesis " features chapters on "Stereoselective Intramolecular J,3-Dipolar Cycloadditions" by I.N.N.

Nambothiiri and A. Hassner giving an in depth survey of the generation and synthetic application of valuable 1,3-dipoles, "4-Acetoxy- and 4-Cyanodioxanes in Synthesis" by C.J. Sinz and S.D. Rychnovsky.

Download STEREOSELECTIVE HETEROCYCLIC SYNTHESIS PDF / Epub free eBooks STEREOSELECTIVE HETEROCYCLIC SYNTHESIS you can download textbooks and business books in PDF format without registration. Download Books free in PDF and ePUB formats. We believe it should be real easy to download your desired books without registration.

Even if you have read one good book. This volume presents exciting new developments in preparative heterocyclic chemistry with a special emphasis on the stereoselective synthesis of - or with the aid of - heterocycles. A wide range of modern methods and strategies for the construction and synthetic elaboration of versatile.

Stereoselective Heterocyclic Synthesis III. Topics in Current Chemistry. Vol. Edited by Peter Metz (Technische Universität Dresden). Springer-Verlag: Berlin, Heidelberg, New York.

x + pp. $ ISBN X. Mark C. McMills. For his work in the area of synthetic organic chemistry, particularly in synthesis of heterocyclic compounds, Meyers was elected to the U.S. National Academy of Sciences in An endowed faculty chair at Colorado State in synthetic organic chemistry and Meyers synthesis.

About this book Introduction This volume presents exciting new developments in preparative heterocyclic chemistry with a special emphasis on the stereoselective synthesis of - or with the aid of. She has authored over 95 publications including reviews in international journals, 12 book chapters in the areas of stereoselective synthesis of heterocyclic compounds and oxidation reactions.

Starting inRenato Dalpozzo was a Researcher of Organic Chemistry at. For his work in the area of synthetic organic chemistry, particularly in synthesis of heterocyclic compounds, Meyers was elected to the U.S.

National Academy of Sciences in An endowed faculty chair at Colorado State in synthetic organic chemistry and Meyers synthesis is named in honor of Meyers. Chapter 3: Stereoselective Non Reviews: 2. Stereoselective Synthesis of Heterocyclic Cage Compounds by Domino Conjugate Additions. Carmen Carreño, Prof.

E-mail address: [email protected] Departamento de Química Orgánica (C‐I), Universidad Autónoma Cantoblanco, Madrid (Spain) Fax: (+34) 91‐‐ Written by a well-respected and experienced author, this textbook fills the gap for a concise introduction to the key concepts of organic stereochemistry and the most important classical and modern methods in stereoselective synthesis.

The concepts are extensively illustrated in color, with practical examples and question-answer sets to help consolidate the readers knowledge. This book provides a noteworthy compilation of the groundbreaking methods of stereoselective synthesis, belonging to the repertoire of every modern practitioner of synthetic organic chemistry.

The general principles underlying these processes are highlighted as they form the basis for the rapid and continuing developments in the field.

The work also features illustrative examples of drug and. The stereoselective synthesis of different aldehydes of a hexahydropyrrolo[1,2-a]pyrazin-4(1H)-one scaffold for modular dipeptide mimetics such as has been reported starting from enantiomerically pure azabicyclic alkenes These intermediates were diols and coupled with a second amino acid.

The product was cleaved at the level of the 1,2-diol with NaIO 4 to give aldehyde In combination with ROM–RCM, rapid access to complex sp 3-rich heterocyclic scaffolds amenable to subsequent functionalization and library synthesis is provided. You have access to this article.

Title:Stereoselective Reactions Catalyzed by N-Heterocyclic Carbenes VOLUME: 15 ISSUE: 4 Author(s):Xiao-Hua Cai* and Bing Xie Affiliation:National School of Medicine, Guizhou Minzu University, GuiyangNational School of Medicine, Guizhou Minzu University, Guiyang Keywords:N-heterocyclic carbene, chiral NHCs, NHCS-mediated reactions, stereoselective reactions Cited by: 2.

19th International Congress on Heterocyclic Chemistry Book of Abstracts.

Description Stereoselective Heterocyclic Synthesis 3 (Topics in Current Chemistry) PDF

Book • Authors: Elsevier. Browse book content. About the book. Search in this book. Search in this book. Browse content Select Stereoselective Synthesis of 2,4-cis-Substituted Pyrrolidines through a Free Radical Sulfur to Carbon Translocation Reaction. A stereoselective synthetic approach to spirooxindole γ-butyrolactams is developed via N-heterocyclic carbene-catalyzed formal [3 + 2] annulation of α-bromoenals with 3-aminooxindoles.

An enantioselective variant of this methodology is also investigated resulting in good substrate tolerance and high enantioselectivities. Armstrong and McAlpine reported a stereoselective synthesis of a tricyclic guanidinium moiety similar to that found in cylindrospermopsin alkaloids.

They employed an intramolecular conjugate addition reaction as a key step in the creation of the piperidine A ring, combined with a Mitsunobu strategy to construct both the B and C rings of the tricycle [].

In combination with ROM–RCM, rapid access to complex sp 3-rich heterocyclic scaffolds amenable to subsequent functionalization and library synthesis is provided. You have access to this articleCited by: 4. In Science of Synthesis: Stereoselective Synthesis expert authors present the best and most reliable methods currently available for the preparation of nonracemic compounds.

These methods may be stoichiometric or catalytic, and the latter may include metal, organic, or enzyme catalysis. The three volumes of Stereoselective Synthesis provide an invaluable resource to the practicing synthetic. Stereoselective Heterocyclic Synthesis I by Peter Metz,available at Book Depository with free delivery worldwide.

Stereoselective Heterocyclic Synthesis I: Peter Metz: We use cookies to give you the best possible experience. In Stereoselective Synthesis expert authors present the best and most reliable methods available for the preparation of nonracemic compounds. These methods may be stoichiometric or catalytic, and the latter may include metal, organic, or enzyme catalysis.

Stereoselective Synthesis 3: Stereoselective Pericyclic Reactions, Cross Coupling, and C—H and C—X Activation N-Heterocyclic Carbene Catalyzed Staudinger Reaction of Ketenes. Thieme eBooks, The major emphasis here is on enantioselective reactions using asymmetric catalysts.

Examples from the total synthesis of various natural and unnatural targets validates the utility of the synthetic methods. Specific topics discussed: cycloaddition, cycloisomerization and sigmatropic rearrangement reactions, allylic and carbonyl functionalization reactions, metal-catalyzed cross.

Thieme E-Books & E-Journals.

Details Stereoselective Heterocyclic Synthesis 3 (Topics in Current Chemistry) FB2

Abstract. A new synthetic strategy for the asymmetric synthesis of five-membered spiropyrazolones via N-heterocyclic carbene-catalyzed [3+2] annulations employing enals and unsaturated pyrazolones as substrates has been developed.

An efficient N-heterocyclic carbene (NHC)-catalyzed asymmetric [3 + 4] annulation reaction of N-Ts hydrazones with 2-bromoenals has been developed. A series of functionalized tetrahydro-1H-1,2-diazepines with two consecutive stereocenters was obtained using NHCs as the catalyst in good yields with excellent diastereo- and by: Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol.

31a. Arene-X (X=Hal, O, S, Se, Te) SOS Knowledge Updates /1 Stereoselective Synthesis 1. Stereoselective Reactions of Carbon–Carbon Double Bonds Stereoselective Synthesis 2.stereoselective syntheses.3, 4 Due to the importance of the aforementioned saturated heterocycles in medicinal and synthetic chemistry, myriad methods have been developed for their synthesis.