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Synthesis of heterocyclic compounds via gold-catalysed enyne rearrangements

Research output: Contribution in Book/Report/Proceedings - With ISBN/ISSNChapter

Published

Standard

Synthesis of heterocyclic compounds via gold-catalysed enyne rearrangements. / Munoz-Herranz, Maria; Quiros Lopez, Maria.
Topics in Heterocyclic Chemistry. ed. / Marco Bandini. Germany: Springer, 2015.

Research output: Contribution in Book/Report/Proceedings - With ISBN/ISSNChapter

Harvard

Munoz-Herranz, M & Quiros Lopez, M 2015, Synthesis of heterocyclic compounds via gold-catalysed enyne rearrangements. in M Bandini (ed.), Topics in Heterocyclic Chemistry. Springer, Germany.

APA

Munoz-Herranz, M., & Quiros Lopez, M. (2015). Synthesis of heterocyclic compounds via gold-catalysed enyne rearrangements. In M. Bandini (Ed.), Topics in Heterocyclic Chemistry Springer.

Vancouver

Munoz-Herranz M, Quiros Lopez M. Synthesis of heterocyclic compounds via gold-catalysed enyne rearrangements. In Bandini M, editor, Topics in Heterocyclic Chemistry. Germany: Springer. 2015

Author

Munoz-Herranz, Maria ; Quiros Lopez, Maria. / Synthesis of heterocyclic compounds via gold-catalysed enyne rearrangements. Topics in Heterocyclic Chemistry. editor / Marco Bandini. Germany : Springer, 2015.

Bibtex

@inbook{87f4c07f53ba4663a870347e1b638d0d,
title = "Synthesis of heterocyclic compounds via gold-catalysed enyne rearrangements",
abstract = "Syntheses of heterocycles using different gold-catalysed rearrangements of enynes are discussed in this chapter. The term skeletal rearrangement has been used in a broad sense to include reactions involving cyclopropyl gold carbene intermediates formed by initial enyne cyclisation, which can undergo many different transformations to give a wide range of heterocyclic structures. Other transformations involving rearrangement of propargylic esters and [3,3]-rearrangement (concerted or stepwise comprising metallic intermediates), as well as special cases, have also been covered. References to earlier work in this area and to recent reviews have been included, but the focus of the chapter is to present recent developments, interesting cases and an overview on how subtle differences in the enyne starting materials, the catalyst used or the reaction conditions can alter the reaction pathway increasing the structural diversity towards complex heterocyclic structures of high value.",
author = "Maria Munoz-Herranz and {Quiros Lopez}, Maria",
year = "2015",
month = dec,
day = "12",
language = "English",
isbn = "1861-9282",
editor = "Marco Bandini",
booktitle = "Topics in Heterocyclic Chemistry",
publisher = "Springer",

}

RIS

TY - CHAP

T1 - Synthesis of heterocyclic compounds via gold-catalysed enyne rearrangements

AU - Munoz-Herranz, Maria

AU - Quiros Lopez, Maria

PY - 2015/12/12

Y1 - 2015/12/12

N2 - Syntheses of heterocycles using different gold-catalysed rearrangements of enynes are discussed in this chapter. The term skeletal rearrangement has been used in a broad sense to include reactions involving cyclopropyl gold carbene intermediates formed by initial enyne cyclisation, which can undergo many different transformations to give a wide range of heterocyclic structures. Other transformations involving rearrangement of propargylic esters and [3,3]-rearrangement (concerted or stepwise comprising metallic intermediates), as well as special cases, have also been covered. References to earlier work in this area and to recent reviews have been included, but the focus of the chapter is to present recent developments, interesting cases and an overview on how subtle differences in the enyne starting materials, the catalyst used or the reaction conditions can alter the reaction pathway increasing the structural diversity towards complex heterocyclic structures of high value.

AB - Syntheses of heterocycles using different gold-catalysed rearrangements of enynes are discussed in this chapter. The term skeletal rearrangement has been used in a broad sense to include reactions involving cyclopropyl gold carbene intermediates formed by initial enyne cyclisation, which can undergo many different transformations to give a wide range of heterocyclic structures. Other transformations involving rearrangement of propargylic esters and [3,3]-rearrangement (concerted or stepwise comprising metallic intermediates), as well as special cases, have also been covered. References to earlier work in this area and to recent reviews have been included, but the focus of the chapter is to present recent developments, interesting cases and an overview on how subtle differences in the enyne starting materials, the catalyst used or the reaction conditions can alter the reaction pathway increasing the structural diversity towards complex heterocyclic structures of high value.

M3 - Chapter

SN - 1861-9282

BT - Topics in Heterocyclic Chemistry

A2 - Bandini, Marco

PB - Springer

CY - Germany

ER -