Palladium(0)-catalyzed allylation of highly acidic and non-nucleophilic arenesulfonamides, sulfamide, and cyanamide. I.

Sílvia Cerezo; Jordi Cortés; Marcial Moreno-Mañas; Roser Pleixats; Anna Roglans

doi:10.1016/S0040-4020(98)00930-2

Palladium(0)-catalyzed allylation of highly acidic and non-nucleophilic arenesulfonamides, sulfamide, and cyanamide. I.

Sílvia Cerezo
, Jordi Cortés
, Marcial Moreno-Mañas
, Roser Pleixats
, Anna Roglans

Autonomous University of Barcelona

Producció científica: Contribució a revista › Article científic › Avaluat per experts

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Resum

Arenesulfonamides, sulfamide, and cyanamide are efficiently allylated using allylic carbonates under Pd(0)-catalysis. N-Arenesulfonyl-2,5- dihydropyrroles are obtained by ruthenium-mediated ring closing metathesis of the corresponding N-diallylated compounds. A stereochemical study of the reactions of ethyl cis-(5-methyl-2-cyclohexenyl) carbonate with 2,4,6- triisopropylphenylsulfonamide was performed, clean overall retention of configuration being found with bidentate phosphines.

Idioma original	Anglès
Pàgines (de-a)	14869-14884
Nombre de pàgines	16
Revista	Tetrahedron
Volum	54
Número	49
DOIs	https://doi.org/10.1016/S0040-4020(98)00930-2
Estat de la publicació	Data de publicació - 3 de des. 1998
Publicat externament	Sí

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@article{0130d689b1fd43e0aceeb655787dbb64,

title = "Palladium(0)-catalyzed allylation of highly acidic and non-nucleophilic arenesulfonamides, sulfamide, and cyanamide. I.",

abstract = "Arenesulfonamides, sulfamide, and cyanamide are efficiently allylated using allylic carbonates under Pd(0)-catalysis. N-Arenesulfonyl-2,5- dihydropyrroles are obtained by ruthenium-mediated ring closing metathesis of the corresponding N-diallylated compounds. A stereochemical study of the reactions of ethyl cis-(5-methyl-2-cyclohexenyl) carbonate with 2,4,6- triisopropylphenylsulfonamide was performed, clean overall retention of configuration being found with bidentate phosphines.",

keywords = "Allylation, Catalysis, Palladium, Stereochemistry",

author = "S{\'i}lvia Cerezo and Jordi Cort{\'e}s and Marcial Moreno-Ma{\~n}as and Roser Pleixats and Anna Roglans",

year = "1998",

month = dec,

day = "3",

doi = "10.1016/S0040-4020(98)00930-2",

language = "English",

volume = "54",

pages = "14869--14884",

journal = "Tetrahedron",

issn = "0040-4020",

publisher = "Elsevier",

number = "49",

}

TY - JOUR

T1 - Palladium(0)-catalyzed allylation of highly acidic and non-nucleophilic arenesulfonamides, sulfamide, and cyanamide. I.

AU - Cerezo, Sílvia

AU - Cortés, Jordi

AU - Moreno-Mañas, Marcial

AU - Pleixats, Roser

AU - Roglans, Anna

PY - 1998/12/3

Y1 - 1998/12/3

N2 - Arenesulfonamides, sulfamide, and cyanamide are efficiently allylated using allylic carbonates under Pd(0)-catalysis. N-Arenesulfonyl-2,5- dihydropyrroles are obtained by ruthenium-mediated ring closing metathesis of the corresponding N-diallylated compounds. A stereochemical study of the reactions of ethyl cis-(5-methyl-2-cyclohexenyl) carbonate with 2,4,6- triisopropylphenylsulfonamide was performed, clean overall retention of configuration being found with bidentate phosphines.

AB - Arenesulfonamides, sulfamide, and cyanamide are efficiently allylated using allylic carbonates under Pd(0)-catalysis. N-Arenesulfonyl-2,5- dihydropyrroles are obtained by ruthenium-mediated ring closing metathesis of the corresponding N-diallylated compounds. A stereochemical study of the reactions of ethyl cis-(5-methyl-2-cyclohexenyl) carbonate with 2,4,6- triisopropylphenylsulfonamide was performed, clean overall retention of configuration being found with bidentate phosphines.

KW - Allylation

KW - Catalysis

KW - Palladium

KW - Stereochemistry

UR - https://www.scopus.com/pages/publications/0032480983

U2 - 10.1016/S0040-4020(98)00930-2

DO - 10.1016/S0040-4020(98)00930-2

M3 - Scientific article

AN - SCOPUS:0032480983

SN - 0040-4020

VL - 54

SP - 14869

EP - 14884

JO - Tetrahedron

JF - Tetrahedron

IS - 49

ER -

Palladium(0)-catalyzed allylation of highly acidic and non-nucleophilic arenesulfonamides, sulfamide, and cyanamide. I.

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