Polyhydroxylated indolizidine alkaloids-synthesis of dideoxycastanospermine

Ari M.P. Koskinen; Oili A. Kallatsa; Maija Nissinen

doi:10.1016/j.tet.2009.09.017

Polyhydroxylated indolizidine alkaloids-synthesis of dideoxycastanospermine

Ari M.P. Koskinen, Oili A. Kallatsa, Maija Nissinen

Tutkimustuotos: Lehtiartikkeli › Article › Scientific › vertaisarvioitu

8 Sitaatiot (Scopus)

395 Lataukset (Pure)

Abstrakti

The key transformation developed in this work is the anti-Kishi selective dihydroxylation, which proceeds by way of intramolecular participation of the nitrogen protecting group to furnish the desired stereochemistry required for castanospermine like structures. In this paper, we completed a first syn-thesis of a novel dideoxycastanospermine 6.

Alkuperäiskieli	Englanti
Sivut	9285-9290
Julkaisu	Tetrahedron
Vuosikerta	65
Numero	45
DOI - pysyväislinkit	https://doi.org/10.1016/j.tet.2009.09.017
Tila	Julkaistu - 2009
OKM-julkaisutyyppi	A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä

Pääsy asiakirjaan

10.1016/j.tet.2009.09.017

ms145Accepted author manuscript, 254 KB

CCDC 648042: Experimental Crystal Structure Determination
Kallatsa, O. A. (Contributor), Koskinen, A. (Creator) & Nissinen, M. (Contributor), Cambridge Crystallographic Data Centre , 1 tammik. 2010
DOI - pysyväislinkki: 10.5517/ccprblb, http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/ccprblb&sid=DataCite
Tietoaineisto: Dataset

Siteeraa tätä

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title = "Polyhydroxylated indolizidine alkaloids-synthesis of dideoxycastanospermine",

abstract = "The key transformation developed in this work is the anti-Kishi selective dihydroxylation, which proceeds by way of intramolecular participation of the nitrogen protecting group to furnish the desired stereochemistry required for castanospermine like structures. In this paper, we completed a first syn-thesis of a novel dideoxycastanospermine 6.",

author = "Koskinen, {Ari M.P.} and Kallatsa, {Oili A.} and Maija Nissinen",

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T1 - Polyhydroxylated indolizidine alkaloids-synthesis of dideoxycastanospermine

AU - Koskinen, Ari M.P.

AU - Kallatsa, Oili A.

AU - Nissinen, Maija

PY - 2009

Y1 - 2009

N2 - The key transformation developed in this work is the anti-Kishi selective dihydroxylation, which proceeds by way of intramolecular participation of the nitrogen protecting group to furnish the desired stereochemistry required for castanospermine like structures. In this paper, we completed a first syn-thesis of a novel dideoxycastanospermine 6.

AB - The key transformation developed in this work is the anti-Kishi selective dihydroxylation, which proceeds by way of intramolecular participation of the nitrogen protecting group to furnish the desired stereochemistry required for castanospermine like structures. In this paper, we completed a first syn-thesis of a novel dideoxycastanospermine 6.

U2 - 10.1016/j.tet.2009.09.017

DO - 10.1016/j.tet.2009.09.017

M3 - Article

SN - 0040-4020

VL - 65

SP - 9285

EP - 9290

JO - Tetrahedron

JF - Tetrahedron

IS - 45

ER -

Polyhydroxylated indolizidine alkaloids-synthesis of dideoxycastanospermine

Abstrakti

Pääsy asiakirjaan

Sormenjälki

Tietoaineistot

CCDC 648042: Experimental Crystal Structure Determination

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