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Sulfur-Mediated Rearrangement II

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Chemistry of non-metals & their compounds, Science, Science/Mathematics, Chemistry - Organic, Organic Chemistry, Rearrangement Reactions, Science / Chemistry / Organic, Sulfur Compounds, Chemistry - Ge
The Physical Object
FormatHardcover
ID Numbers
Open LibraryOL12810163M
ISBN 103540680993
ISBN 139783540680994

Thione–Thiol Rearrangement: Miyazaki–Newman–Kwart Rearrangement and Others Cristiano Zonta, Ottorino De Lucchi, Raffaella Volpicelli, Livius Cotarca Pages *immediately available upon purchase as print book shipments may be delayed due to the COVID crisis. ebook access is temporary and does not include ownership of the ebook.

Only valid for books with an ebook version. Plesniak, A. Zarecki, J. Wicha: The Smiles Rearrangement and the Julia-Kocienski Olefination Reaction: Series Title: Topics in current chemistry, Other Titles: Sulfur-mediated rearrangements two Sulfur-mediated rearrangements 2: Responsibility: volume editor, Ernst Schaumann ; with contributions by S.

Braverman [and others]. Find many great new & used options and get the best deals for Topics in Current Chemistry: Sulfur-Mediated Rearrangements II Vol. 2 (, Hardcover) at the best online prices at eBay.

Free shipping for many products. Genre/Form: Electronic books: Additional Physical Format: Print version: Sulfur-mediated rearrangements II. Berlin ; New York: Springer, © (OCoLC) Sulfur-Mediated Rearrangements II Michael Reggelin (auth.), Ernst Schaumann (eds.) M.

Reggelin: [2,3]-Sigmatropic Rearrangements of Allylic Sulfur Compounds Series: Topics in Current Chemistry () (Book ) Hardcover: pages Publisher: Springer; edition (Febru ) Language: English ISBN ISBN ASIN: Product Dimensions: x x inches Shipping Weight: 1 pounds (View shipping rates and policies) Customer Reviews: Be the first to write a reviewFormat: Hardcover.

Sulfur-Mediated Rearrangements I Ernst Schaumann (auth.), Ernst Schaumann (eds.) E. Schaumann: Sulfur is More than the Fat Brother of Oxygen. rearrangement pummerer synthesis carbon thio mechanism acid tetrahedron yield chemistry You can write a book review and share your experiences.

Other. The rearrangement of sulfonium salts and sulfoxides takes place even more readily. Alkenylsulfoxides and sulfilimines undergo a highly stereocontrolled cyclization to lactones and lactams,respectively, upon reaction with haloketenes; this synthetically useful process entails a [3,3]-sigmatropicrearrangement of a zwitterionic by: Sulfur-Mediated Rearrangements II Volume Editor: Ernst Schaumann Contents of Volume Sulfur-Mediated Rearrangements I Volume Editor: Ernst Schaumann ISBN: (cited at the beginning of each section related to a particular rearrangement) and book chapters [2–5].

Excellent treatments with particular emphasis on. The development of a direct ylide transfer to carbonyl derivatives and of a sulfoxide-mediated arylation is presented from a unified perspective. Mechanistic studies (including density functional calculations) support a common reaction pathway and showcase how subtle changes in reactant properties can lead to disparate and seemingly unrelated reaction outcomes.

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Rearrangements Involving Sulfones. Samuel Braverman. Department of Chemistry, Bar‐Ilan University, Ramat‐GanIsrael The Ramberg– Bäcklund Rearrangement. The Smiles and Related Rearrangements. Miscellaneous Rearrangements. Sulfur-Mediated Rearrangements II, /_, (), (). by: 5. [2,3]Sigmatropic rearrangements of propargyl sulfonium ylides along with recent advances in the correspondingsulfenate-sulfoxide and sulfinate-sulfone type rearrangements are reviewed.

Request PDF | Anti-Markovnikov rearrangement in sulfur mediated allylic C–H amination of olefins | Cationic rearrangement reactions usually follow Markovnikov's rule to. Hollow one-dimensional (1-D) nanostructures have drawn great attention in heterogeneous photocatalysis.

Herein, we report that tapered polyacrylonitrile-derived carbon (C-PAN)/g-C3N4 composite nanotubes can be synthesized through a facile sulfur-mediated self-templating method via thermal condensation of polyacrylonitrile (PAN), melamine, and by:   1. Angew Chem Int Ed Engl. Feb 24;55(9) doi: /anie Epub Jan Elemental-Sulfur-Mediated Facile Synthesis of a Covalent Triazine Framework for High-Performance Lithium-Sulfur by:   Recently, our group has developed a flexible domino process for the synthesis of carbocycles.

1 This is based on the one-pot reaction of silyl-substituted thioacetal carbanions as dianion equivalents with epoxy-tosylates.

Following epoxide ring opening by the carbanion, a reversible C→O silyl migration (Brook rearrangement) 2 is the key step. The method has Cited by: 4. The inefficient pπ –pπ C = S bond is the basis for the thione-thiol (Newman–Kwart) rearrangement (see “Thione-thiol Rearrangement: Newman– Kwart Rearrangement and Others” by C.

Zonta, O. de Lucci, R.

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Volpicelli and L. Cotarca, in this volume) and is an interesting feature in the efficiency of [] sigmatropic rearrangements of. Typical procedure for the sulfur-mediated C(sp 2)-H imidation and 1,2-imidofluorination. To a mL reaction tube was sequentially added vinyl sulfide 3 ( mmol), dry acetonitrile (1 mL), and N-fluorobis(benzenesulfonyl)imide ( mg, mmol).

The system was quickly sealed with a Teflon cap and immersed into an 80 °C by: 5. Purchase Comprehensive Organic Synthesis - 2nd Edition.

Print Book & E-Book. ISBN  Elemental sulfur mediated decarboxylative redox cyclization reaction of o-chloronitroarenes and arylacetic acids. Guntreddi T(1), Vanjari R, Singh KN. Author information: (1)Department of Chemistry (Centre of Advanced Study), Faculty of Science, Banaras Hindu University, Varanasi, by: Sulfur-Mediated Rearrangement II SchaumannApprox.

Also available online., Hardcover Organometallic Oxidation Catalysis Meyer Topics in Organometallic ChemistryApprox. Also available online., Hardcover Organometallic Chemistry. An oxidative cyclization of 2-aminothiophenols and arylacetylenes or styrenes for the synthesis of 2-alkylbenzothiazoles and 2-acylbenzothiazoles has been developed.

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Elemental sulfur was used as the effective oxidant to give the corresponding product in good yield under metal-free conditions.

Synthetic methodology in OBCCited by: 6. 6a For selected review on sulfur-mediated [2,3]-sigmatropic rearrangements, see: Topics in Current Chemistry Vol. Springer; Berlin: 6b For selected review on sulfur-mediated Belluš-Claisen rearrangements, see: Bonda J. Angew.

Chem. Int. by: New Abstracts. Abstracts of articles in the field of organic synthesis, published in the most highly regarded organic chemistry journals. Iridium(I)-Catalyzed C-C and C-N Bond Formation Reactions via the Borrowing Hydrogen Strategy S.

Genç, B. Arslan, S. Gülcemal, S. Günnaz, B. Çetinkaya, D. Gülcemal, J. Org. Chem.,84, Facile synthesis of a variety of α-heterosubstituted ketones under mild conditions was achieved by copper-mediated cross-coupling of thioesters with functionalized organostannanes.

Application of this coupling methodology provided a concise pathway for the conversion of carboxylic acids to 2-aminoimidazoles, 2-aminothiazoles, and 2-aminooxazoles via thioesters in practical by: 9. Kannan, Muthukumar; Muthaiah, Senthilkumar: Ruthenium(II)-Complex-Catalyzed Acceptorless Double Dehydrogenation of Primary Amines to Nitriles Full Text HTML.

Application of Modern X-ray Spectroscopy in Chemistry—Beyond Studying the Oxidation StateCited by: 4. PeBook Info List Added Wang, Lawrence K. ; Hung, Yung-Tse; Shammas, Nazih K.

Cölfen, Helmut; Wandrey, Christine The platinum(II) catalyst was also used in a study on the influence of alkene substitution on pentaene cyclizations (Scheme). Three unique analogues (,and ) of pentaeneswith different methyl group modification, were synthesized and treated with catalystinducing polyene cyclizations to provide the cyclized Cited by: 9.

Sulfur-Mediated Rearrangements I de - English books - commander la livre de la catégorie Chimie sans frais de port et bon marché - Ex Libris boutique en ligne.This banner text can have markup. web; books; video; audio; software; images; Toggle navigation.Examples of copper(II) catalysts include the 1,4,7-triazacyclononane comp which requires a rather large excess of olen [42], copper(II) acetylacetonate immobilized in ionic liquids (entry 7), which can be recycled many times without loss of activity [43], and Cu2 exchanged zeolite Y (CuHY) in acetonitrile (entry 8), which allows for 5/5(1).