Sequential Oxidative and Reductive Radical Cyclization Approach toward Asperparaline C and Synthesis of Its 8-Oxo Analogue

Tynchtyk Amatov; Radek Pohl; Ivana Cisařová; Ullrich Jahn

doi:10.1021/acs.orglett.7b00187

Sequential Oxidative and Reductive Radical Cyclization Approach toward Asperparaline C and Synthesis of Its 8-Oxo Analogue

Tynchtyk Amatov, Radek Pohl, Ivana Cisařová, Ullrich Jahn

Chemistry

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

Abstract

The most advanced approach, so far, to the asperparalines is developed. Consecutive oxidative and reductive radical cyclizations serve as the key steps to stereoselectively access the complex fully elaborated skeleton containing the cyclopentane and spiro-succinimide units.

Original language	English (US)
Pages (from-to)	1152-1155
Number of pages	4
Journal	Organic Letters
Volume	19
Issue number	5
DOIs	https://doi.org/10.1021/acs.orglett.7b00187
State	Published - Mar 3 2017

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/acs.orglett.7b00187

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title = "Sequential Oxidative and Reductive Radical Cyclization Approach toward Asperparaline C and Synthesis of Its 8-Oxo Analogue",

abstract = "The most advanced approach, so far, to the asperparalines is developed. Consecutive oxidative and reductive radical cyclizations serve as the key steps to stereoselectively access the complex fully elaborated skeleton containing the cyclopentane and spiro-succinimide units.",

author = "Tynchtyk Amatov and Radek Pohl and Ivana Cisa{\v r}ov{\'a} and Ullrich Jahn",

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AU - Pohl, Radek

AU - Cisařová, Ivana

AU - Jahn, Ullrich

PY - 2017/3/3

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Sequential Oxidative and Reductive Radical Cyclization Approach toward Asperparaline C and Synthesis of Its 8-Oxo Analogue

Abstract

ASJC Scopus subject areas

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