Palladium-Catalyzed Formal (5 + 2) Annulation between ortho-Alkenylanilides and Allenes

Borja Cendón; Noelia Casanova; Cezar C. Comanescu; Rebeca García-Fandiño; Andrés Seoane; Moisés Gulías; José L. Mascareñas

doi:10.1021/acs.orglett.7b00467

Palladium-Catalyzed Formal (5 + 2) Annulation between ortho-Alkenylanilides and Allenes

Borja Cendón, Noelia Casanova, Cezar C. Comanescu, Rebeca García-Fandiño, Andrés Seoane, Moisés Gulías, José L. Mascareñas

Producció científica: Article en revista indexada › Article › Avaluat per experts

49 Cites (Scopus)

Resum

2-Alkenyltriflylanilides react with allenes upon treatment with catalytic amounts of Pd(OAc)₂ and Cu(II) to give highly valuable 2,3-dihydro-1H-benzo[b]azepines, in good yields, and with very high regio- and diastereoselectivities. Density functional theory (DFT) calculations suggest that the C-H activation of the alkenylanilide involves a classical concerted metalation-deprotonation (CMD) mechanism.

Idioma original	Anglès
Pàgines (de-a)	1674-1677
Nombre de pàgines	4
Revista	Organic Letters
Volum	19
Número	7
DOIs	https://doi.org/10.1021/acs.orglett.7b00467
Estat de la publicació	Publicada - 7 d’abr. 2017
Publicat externament	Sí

Accés al document

10.1021/acs.orglett.7b00467

Altres arxius i enllaços

Enllaç a la publicació de Scopus

Com citar-ho

@article{879bf70fb7e24062bf5e233f2085ef8c,

title = "Palladium-Catalyzed Formal (5 + 2) Annulation between ortho-Alkenylanilides and Allenes",

abstract = "2-Alkenyltriflylanilides react with allenes upon treatment with catalytic amounts of Pd(OAc)2 and Cu(II) to give highly valuable 2,3-dihydro-1H-benzo[b]azepines, in good yields, and with very high regio- and diastereoselectivities. Density functional theory (DFT) calculations suggest that the C-H activation of the alkenylanilide involves a classical concerted metalation-deprotonation (CMD) mechanism.",

author = "Borja Cend{\'o}n and Noelia Casanova and Comanescu, {Cezar C.} and Rebeca Garc{\'i}a-Fandi{\~n}o and Andr{\'e}s Seoane and Mois{\'e}s Gul{\'i}as and Mascare{\~n}as, {Jos{\'e} L.}",

note = "Publisher Copyright: {\textcopyright} 2017 American Chemical Society.",

year = "2017",

month = apr,

day = "7",

doi = "10.1021/acs.orglett.7b00467",

language = "English",

volume = "19",

pages = "1674--1677",

journal = "Organic Letters",

issn = "1523-7060",

publisher = "American Chemical Society",

number = "7",

}

TY - JOUR

T1 - Palladium-Catalyzed Formal (5 + 2) Annulation between ortho-Alkenylanilides and Allenes

AU - Cendón, Borja

AU - Casanova, Noelia

AU - Comanescu, Cezar C.

AU - García-Fandiño, Rebeca

AU - Seoane, Andrés

AU - Gulías, Moisés

AU - Mascareñas, José L.

PY - 2017/4/7

Y1 - 2017/4/7

N2 - 2-Alkenyltriflylanilides react with allenes upon treatment with catalytic amounts of Pd(OAc)2 and Cu(II) to give highly valuable 2,3-dihydro-1H-benzo[b]azepines, in good yields, and with very high regio- and diastereoselectivities. Density functional theory (DFT) calculations suggest that the C-H activation of the alkenylanilide involves a classical concerted metalation-deprotonation (CMD) mechanism.

AB - 2-Alkenyltriflylanilides react with allenes upon treatment with catalytic amounts of Pd(OAc)2 and Cu(II) to give highly valuable 2,3-dihydro-1H-benzo[b]azepines, in good yields, and with very high regio- and diastereoselectivities. Density functional theory (DFT) calculations suggest that the C-H activation of the alkenylanilide involves a classical concerted metalation-deprotonation (CMD) mechanism.

UR - http://www.scopus.com/inward/record.url?scp=85017172705&partnerID=8YFLogxK

U2 - 10.1021/acs.orglett.7b00467

DO - 10.1021/acs.orglett.7b00467

M3 - Article

C2 - 28345930

AN - SCOPUS:85017172705

SN - 1523-7060

VL - 19

SP - 1674

EP - 1677

JO - Organic Letters

JF - Organic Letters

IS - 7

ER -

Palladium-Catalyzed Formal (5 + 2) Annulation between ortho-Alkenylanilides and Allenes

Resum

Accés al document

Altres arxius i enllaços

Fingerprint

Com citar-ho