Highly enantio- and diastereoselective one-pot reactions in aqueous media: Combined asymmetric Rh-catalyzed conjugate addition/metal-mediated allylation

S Kallstrom; Jagt RBC; R Sillanpaa; BL Feringa; AJ Minnaard; Reko Leino

doi:10.1002/ejoc.200600309

Highly enantio- and diastereoselective one-pot reactions in aqueous media: Combined asymmetric Rh-catalyzed conjugate addition/metal-mediated allylation

S Kallstrom
, Jagt RBC
, R Sillanpaa
, BL Feringa
, AJ Minnaard
, Reko Leino

Tutkimustuotos: Lehtiartikkeli › Artikkeli › Tieteellinen › vertaisarvioitu

19 Sitaatiot (Scopus)

Abstrakti

1,3-Disubstituted, enantiopure cyclohexanols have been prepared in very high diastereoselectivities and good yields by a concise one-pot method combining the enantioselective rhodium-catalyzed conjugate addition of arylboronic acids with indium-mediated allylation into a highly efficient one-pot reaction in aqueous media. (c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006.

Alkuperäiskieli	Ei tiedossa
Sivut	3826–3833
Sivumäärä	8
Julkaisu	European Journal of Organic Chemistry
Vuosikerta	2006
Numero	17
DOI - pysyväislinkit	https://doi.org/10.1002/ejoc.200600309
Tila	Julkaistu - 2006
OKM-julkaisutyyppi	A1 Julkaistu artikkeli, soviteltu

Keywords

allylation
conjugate addition
diastereoselectivity
asymmetric synthesis

Pääsy asiakirjaan

10.1002/ejoc.200600309

Viittausmuodot

@article{9e8fc52a3b124478936f95b01621f4b0,

title = "Highly enantio- and diastereoselective one-pot reactions in aqueous media: Combined asymmetric Rh-catalyzed conjugate addition/metal-mediated allylation",

abstract = "1,3-Disubstituted, enantiopure cyclohexanols have been prepared in very high diastereoselectivities and good yields by a concise one-pot method combining the enantioselective rhodium-catalyzed conjugate addition of arylboronic acids with indium-mediated allylation into a highly efficient one-pot reaction in aqueous media. (c) Wiley-VCH Verlag GmbH \& Co. KGaA, 69451 Weinheim, Germany, 2006.",

keywords = "allylation, conjugate addition, diastereoselectivity, asymmetric synthesis, allylation, conjugate addition, diastereoselectivity, asymmetric synthesis, allylation, conjugate addition, diastereoselectivity, asymmetric synthesis",

author = "S Kallstrom and Jagt RBC and R Sillanpaa and BL Feringa and AJ Minnaard and Reko Leino",

year = "2006",

doi = "10.1002/ejoc.200600309",

language = "Odefinierat/ok{\"a}nt",

volume = "2006",

pages = "3826{\textendash}3833",

journal = "European Journal of Organic Chemistry",

issn = "1434-193X",

publisher = "Wiley",

number = "17",

}

Highly enantio- and diastereoselective one-pot reactions in aqueous media: Combined asymmetric Rh-catalyzed conjugate addition/metal-mediated allylation. / Kallstrom, S; RBC, Jagt; Sillanpaa, R et al.
julkaisussa: European Journal of Organic Chemistry, Vuosikerta 2006, Nro 17, 2006, s. 3826–3833.

Tutkimustuotos: Lehtiartikkeli › Artikkeli › Tieteellinen › vertaisarvioitu

TY - JOUR

T1 - Highly enantio- and diastereoselective one-pot reactions in aqueous media: Combined asymmetric Rh-catalyzed conjugate addition/metal-mediated allylation

AU - Kallstrom, S

AU - RBC, Jagt

AU - Sillanpaa, R

AU - Feringa, BL

AU - Minnaard, AJ

AU - Leino, Reko

PY - 2006

Y1 - 2006

N2 - 1,3-Disubstituted, enantiopure cyclohexanols have been prepared in very high diastereoselectivities and good yields by a concise one-pot method combining the enantioselective rhodium-catalyzed conjugate addition of arylboronic acids with indium-mediated allylation into a highly efficient one-pot reaction in aqueous media. (c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006.

AB - 1,3-Disubstituted, enantiopure cyclohexanols have been prepared in very high diastereoselectivities and good yields by a concise one-pot method combining the enantioselective rhodium-catalyzed conjugate addition of arylboronic acids with indium-mediated allylation into a highly efficient one-pot reaction in aqueous media. (c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006.

KW - allylation

KW - conjugate addition

KW - diastereoselectivity

KW - asymmetric synthesis

KW - allylation

KW - conjugate addition

KW - diastereoselectivity

KW - asymmetric synthesis

KW - allylation

KW - conjugate addition

KW - diastereoselectivity

KW - asymmetric synthesis

U2 - 10.1002/ejoc.200600309

DO - 10.1002/ejoc.200600309

M3 - Artikel

SN - 1434-193X

VL - 2006

SP - 3826

EP - 3833

JO - European Journal of Organic Chemistry

JF - European Journal of Organic Chemistry

IS - 17

ER -