Alkynes in Cycloadditions (Electronic book text, 1st edition)


Acetylene systems present a new route to cyclic compounds as an alternative to more traditional methods employed in classical organic chemistry. The synthesis of cyclic structures based on acetylene systems has important applications in the formation of nanostructures, naturally occurring compounds and chemosensory materials for the design of nonlinear optics, electronic and photonic devices.

"Alkynes in Cycloadditions" presents a modern review of regioselective synthesis of aromatic and non-aromatic carbocyclic and heterocyclic ring systems based primarily on 2]2+2] and 4]2] cycloadditions, and other reactions of acetylenic units including enediynes and enyne-allenes.

Topics covered include: New strategies for the formation of aromatic and polynuclear hydrocarbons based on (Z)-hex-3-en-1,5-diyne and (Z)-hepta-1,2,4-triene-6-yne blocks.One-step synthesis of benzene derivatives, β-substituted naphthalenes and acenes by the cycloaromatization of enediynes and enyne-allenes by Bergman, Myers-Saito and Shmittel.Mechanisms of cycloaromatization resulting in the formation of fulvene and indene systems.Heterocyclization involving enyne-carbodiimides.New achievements in classical cycloaddition reactions such as the Diels-Alder condensation with acetylenic dienophiles and 2]2] cycloadditions with acetylene components

"Alkynes in Cycloadditions" presents a comprehensive summary of the literature on methods for the synthesis of ring systems from acetylenes for academic researchers working in the fields of organic synthesis, physical organic chemistry, organometallic chemistry, catalysis, materials science, nanomaterials and biochemistry.


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Product Description

Acetylene systems present a new route to cyclic compounds as an alternative to more traditional methods employed in classical organic chemistry. The synthesis of cyclic structures based on acetylene systems has important applications in the formation of nanostructures, naturally occurring compounds and chemosensory materials for the design of nonlinear optics, electronic and photonic devices.

"Alkynes in Cycloadditions" presents a modern review of regioselective synthesis of aromatic and non-aromatic carbocyclic and heterocyclic ring systems based primarily on 2]2+2] and 4]2] cycloadditions, and other reactions of acetylenic units including enediynes and enyne-allenes.

Topics covered include: New strategies for the formation of aromatic and polynuclear hydrocarbons based on (Z)-hex-3-en-1,5-diyne and (Z)-hepta-1,2,4-triene-6-yne blocks.One-step synthesis of benzene derivatives, β-substituted naphthalenes and acenes by the cycloaromatization of enediynes and enyne-allenes by Bergman, Myers-Saito and Shmittel.Mechanisms of cycloaromatization resulting in the formation of fulvene and indene systems.Heterocyclization involving enyne-carbodiimides.New achievements in classical cycloaddition reactions such as the Diels-Alder condensation with acetylenic dienophiles and 2]2] cycloadditions with acetylene components

"Alkynes in Cycloadditions" presents a comprehensive summary of the literature on methods for the synthesis of ring systems from acetylenes for academic researchers working in the fields of organic synthesis, physical organic chemistry, organometallic chemistry, catalysis, materials science, nanomaterials and biochemistry.

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Product Details

General

Imprint

John Wiley & Sons

Country of origin

United States

Release date

October 2013

Availability

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First published

2014

Authors

Translators

Consultant editors

Format

Electronic book text

Pages

272

Edition

1st edition

ISBN-13

978-1-118-70933-7

Barcode

9781118709337

Categories

LSN

1-118-70933-0



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