Электронная книга: John Tebby C. «Alkynes in Cycloadditions»

Alkynes in Cycloadditions

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.

Издательство: "John Wiley&Sons Limited"

ISBN: 9781118709337

электронная книга

Купить за 15134.89 руб и скачать на Litres

Другие книги схожей тематики:

АвторКнигаОписаниеГодЦенаТип книги

См. также в других словарях:

  • Azide alkyne Huisgen cycloaddition — The Azide Alkyne Huisgen Cycloaddition is a 1,3 dipolar cycloaddition between an azide and a terminal or internal alkyne to give a 1,2,3 triazole. Rolf Huisgen[1] was the first to understand the scope of this organic reaction. American chemist K …   Wikipedia

  • 1,3-Dipolar cycloaddition — The 1,3 dipolar cycloaddition, also known as the Huisgen cycloaddition or Huisgen reaction, [1][2] is an organic chemical reaction belonging to the larger class of concerted, pericyclic cycloadditions. It is the reaction between a 1,3 dipole and… …   Wikipedia

  • Nitrone-olefin 3+2 cycloaddition — The correct title of this article is Nitrone olefin [3+2] cycloaddition. The substitution or omission of any < > [ ] { } is due to technical restrictions. The nitrone olefin [3+2] cycloaddition reaction is the combination of a nitrone with… …   Wikipedia

  • Азид-алкиновое циклоприсоединение — Азид алкиновое циклоприсоединение  реакция между азидами и алкинами с образованием 1,2,3 триазолов. Реакция впервые была описана Михаэлем в 1893 г., который обнаружил, что при нагреве эфирного раствора фенилазида и диметилового эфира… …   Википедия

  • Alkyne trimerisation — An alkyne trimerisation reaction is a 2+2+2 cyclization reaction in which three alkyne molecules react to form an aromatic compound. The reaction is pseudo pericyclic since it has not been observed to occur without the assistance of metal… …   Wikipedia

  • Click chemistry — is a chemical philosophy introduced by K. Barry Sharpless of The Scripps Research Institute, in 2001[1][2] and describes chemistry tailored to generate substances quickly and reliably by joining small units together. This is inspired by the fact… …   Wikipedia

Поделиться ссылкой на выделенное

Прямая ссылка:
Нажмите правой клавишей мыши и выберите «Копировать ссылку»