Asymmetric synthesis of (+)-tetrahydropseudodistomin

S. Chandrasekhar; S. Shameem Sultana; N. Kiranmai; Ch Narsihmulu

doi:10.1016/j.tetlet.2007.01.143

Asymmetric synthesis of (+)-tetrahydropseudodistomin

S. Chandrasekhar, S. Shameem Sultana, N. Kiranmai, Ch Narsihmulu

Research output: Contribution to journal › Article › peer-review

11 Scopus citations

Abstract

An efficient asymmetric synthesis of (+)-tetrahydropseudodistomin is described. The important synthetic features include a Maruoka asymmetric allylation and a Sharpless asymmetric dihydroxylation as key steps for the generation of chirality at C-2, -4, and -5 of the trisubstituted piperidine ring.

Original language	English (US)
Pages (from-to)	2373-2375
Number of pages	3
Journal	Tetrahedron Letters
Volume	48
Issue number	13
DOIs	https://doi.org/10.1016/j.tetlet.2007.01.143
State	Published - Mar 26 2007
Externally published	Yes

Bibliographical note

Funding Information:
S.S.S. thanks the CSIR, New Delhi and N.K. thanks the UGC, New Delhi, for financial support and S.C. thanks the DST, New Delhi, for a grant.

Keywords

Marouka asymmetric allylation
Sharpless asymmetric dihydroxylation

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title = "Asymmetric synthesis of (+)-tetrahydropseudodistomin",

abstract = "An efficient asymmetric synthesis of (+)-tetrahydropseudodistomin is described. The important synthetic features include a Maruoka asymmetric allylation and a Sharpless asymmetric dihydroxylation as key steps for the generation of chirality at C-2, -4, and -5 of the trisubstituted piperidine ring.",

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author = "S. Chandrasekhar and {Shameem Sultana}, S. and N. Kiranmai and Ch Narsihmulu",

note = "Funding Information: S.S.S. thanks the CSIR, New Delhi and N.K. thanks the UGC, New Delhi, for financial support and S.C. thanks the DST, New Delhi, for a grant.",

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T1 - Asymmetric synthesis of (+)-tetrahydropseudodistomin

AU - Chandrasekhar, S.

AU - Shameem Sultana, S.

AU - Kiranmai, N.

AU - Narsihmulu, Ch

N1 - Funding Information: S.S.S. thanks the CSIR, New Delhi and N.K. thanks the UGC, New Delhi, for financial support and S.C. thanks the DST, New Delhi, for a grant.

PY - 2007/3/26

Y1 - 2007/3/26

N2 - An efficient asymmetric synthesis of (+)-tetrahydropseudodistomin is described. The important synthetic features include a Maruoka asymmetric allylation and a Sharpless asymmetric dihydroxylation as key steps for the generation of chirality at C-2, -4, and -5 of the trisubstituted piperidine ring.

AB - An efficient asymmetric synthesis of (+)-tetrahydropseudodistomin is described. The important synthetic features include a Maruoka asymmetric allylation and a Sharpless asymmetric dihydroxylation as key steps for the generation of chirality at C-2, -4, and -5 of the trisubstituted piperidine ring.

KW - Marouka asymmetric allylation

KW - Sharpless asymmetric dihydroxylation

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EP - 2375

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 13

ER -

Asymmetric synthesis of (+)-tetrahydropseudodistomin

Abstract

Bibliographical note

Keywords

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