Stereodivergent synthesis of pseudotabersonine alkaloids

Mihail Kazak; Martins Priede; Kirill Shubin; Hannah E. Bartrum; Jean François Poisson; Edgars Suna

doi:10.1021/acs.orglett.7b02635

Stereodivergent synthesis of pseudotabersonine alkaloids

Mihail Kazak
, Martins Priede
, Kirill Shubin
, Hannah E. Bartrum
, Jean François Poisson
, Edgars Suna^*

^*Corresponding author for this work

Latvian Institute of Organic Synthesis
Université Grenoble Alpes

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

11 Citations (Scopus)

Abstract

An eight-step stereodivergent synthesis of enantiomerically pure (-)-14-epi-pseudotabersonine and (+)-pseudotabersonine has been developed from a common N-tert-butanesulfinyl ketimine key intermediate.

Original language	English
Pages (from-to)	5356-5359
Number of pages	4
Journal	Organic Letters
Volume	19
Issue number	19
DOIs	https://doi.org/10.1021/acs.orglett.7b02635
Publication status	Published - 6 Oct 2017
Externally published	Yes

OECD Field of Science

1.4 Chemical Sciences

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10.1021/acs.orglett.7b02635

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@article{98d37cace7064d14a0abc127d774fb5a,

title = "Stereodivergent synthesis of pseudotabersonine alkaloids",

abstract = "An eight-step stereodivergent synthesis of enantiomerically pure (-)-14-epi-pseudotabersonine and (+)-pseudotabersonine has been developed from a common N-tert-butanesulfinyl ketimine key intermediate.",

author = "Mihail Kazak and Martins Priede and Kirill Shubin and Bartrum, \{Hannah E.\} and Poisson, \{Jean Fran{\c c}ois\} and Edgars Suna",

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

year = "2017",

month = oct,

day = "6",

doi = "10.1021/acs.orglett.7b02635",

language = "English",

volume = "19",

pages = "5356--5359",

journal = "Organic Letters",

issn = "1523-7060",

publisher = "American Chemical Society",

number = "19",

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TY - JOUR

T1 - Stereodivergent synthesis of pseudotabersonine alkaloids

AU - Kazak, Mihail

AU - Priede, Martins

AU - Shubin, Kirill

AU - Bartrum, Hannah E.

AU - Poisson, Jean François

AU - Suna, Edgars

PY - 2017/10/6

Y1 - 2017/10/6

N2 - An eight-step stereodivergent synthesis of enantiomerically pure (-)-14-epi-pseudotabersonine and (+)-pseudotabersonine has been developed from a common N-tert-butanesulfinyl ketimine key intermediate.

AB - An eight-step stereodivergent synthesis of enantiomerically pure (-)-14-epi-pseudotabersonine and (+)-pseudotabersonine has been developed from a common N-tert-butanesulfinyl ketimine key intermediate.

UR - https://www.scopus.com/pages/publications/85032646779

U2 - 10.1021/acs.orglett.7b02635

DO - 10.1021/acs.orglett.7b02635

M3 - Article

C2 - 28901770

AN - SCOPUS:85032646779

SN - 1523-7060

VL - 19

SP - 5356

EP - 5359

JO - Organic Letters

JF - Organic Letters

IS - 19

ER -

Stereodivergent synthesis of pseudotabersonine alkaloids

Abstract

OECD Field of Science

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