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Silver and platinum-catalysed addition of O–H and N–H bonds to allenes

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Silver and platinum-catalysed addition of O–H and N–H bonds to allenes. / Munoz-Herranz, Maria.
In: Chemical Society Reviews, Vol. 43, No. 9, 25.03.2014, p. 3164-3183.

Research output: Contribution to Journal/Magazine › Journal article › peer-review

Harvard

Munoz-Herranz, M 2014, 'Silver and platinum-catalysed addition of O–H and N–H bonds to allenes', Chemical Society Reviews, vol. 43, no. 9, pp. 3164-3183. https://doi.org/10.1039/c3cs60408j

APA

Munoz-Herranz, M. (2014). Silver and platinum-catalysed addition of O–H and N–H bonds to allenes. Chemical Society Reviews, 43(9), 3164-3183. https://doi.org/10.1039/c3cs60408j

Vancouver

Munoz-Herranz M. Silver and platinum-catalysed addition of O–H and N–H bonds to allenes. Chemical Society Reviews. 2014 Mar 25;43(9):3164-3183. doi: 10.1039/c3cs60408j

Author

Munoz-Herranz, Maria. / Silver and platinum-catalysed addition of O–H and N–H bonds to allenes. In: Chemical Society Reviews. 2014 ; Vol. 43, No. 9. pp. 3164-3183.

Bibtex

@article{65bd2b775ca64d6e90f953bd5e2adf74,
title = "Silver and platinum-catalysed addition of O–H and N–H bonds to allenes",
abstract = "Transition-metal catalysed nucleophile addition to allenes is a very powerful tool for the synthesis of functionalised molecules containing heteroatoms, heterocycles in the intramolecular version, or allyl derivatives in the intermolecular version. The reaction has been explored with a wide variety of metals, silver being one of the most effective. Although platinum has somehow been less explored, different reactivities have been observed with this metal, showing the great potential and versatility of this methodology. This review will highlight the reactions with these two metals, silver and platinum, when oxygen or nitrogen nucleophiles are employed. Although most of the examples describe the intramolecular version, some intermolecular reactions with platinum have been described, and will also be covered.",
author = "Maria Munoz-Herranz",
year = "2014",
month = mar,
day = "25",
doi = "10.1039/c3cs60408j",
language = "English",
volume = "43",
pages = "3164--3183",
journal = "Chemical Society Reviews",
issn = "0306-0012",
publisher = "American Chemical Society",
number = "9",

}

RIS

TY - JOUR

T1 - Silver and platinum-catalysed addition of O–H and N–H bonds to allenes

AU - Munoz-Herranz, Maria

PY - 2014/3/25

Y1 - 2014/3/25

N2 - Transition-metal catalysed nucleophile addition to allenes is a very powerful tool for the synthesis of functionalised molecules containing heteroatoms, heterocycles in the intramolecular version, or allyl derivatives in the intermolecular version. The reaction has been explored with a wide variety of metals, silver being one of the most effective. Although platinum has somehow been less explored, different reactivities have been observed with this metal, showing the great potential and versatility of this methodology. This review will highlight the reactions with these two metals, silver and platinum, when oxygen or nitrogen nucleophiles are employed. Although most of the examples describe the intramolecular version, some intermolecular reactions with platinum have been described, and will also be covered.

AB - Transition-metal catalysed nucleophile addition to allenes is a very powerful tool for the synthesis of functionalised molecules containing heteroatoms, heterocycles in the intramolecular version, or allyl derivatives in the intermolecular version. The reaction has been explored with a wide variety of metals, silver being one of the most effective. Although platinum has somehow been less explored, different reactivities have been observed with this metal, showing the great potential and versatility of this methodology. This review will highlight the reactions with these two metals, silver and platinum, when oxygen or nitrogen nucleophiles are employed. Although most of the examples describe the intramolecular version, some intermolecular reactions with platinum have been described, and will also be covered.

U2 - 10.1039/c3cs60408j

DO - 10.1039/c3cs60408j

M3 - Journal article

VL - 43

SP - 3164

EP - 3183

JO - Chemical Society Reviews

JF - Chemical Society Reviews

SN - 0306-0012

IS - 9

ER -