Stereoselective construction of a key hydroindole precursor of epidithiodiketopiperazine (ETP) natural products

Minghao Feng; Xuefeng Jiang

doi:10.1039/c4cc04148h

Stereoselective construction of a key hydroindole precursor of epidithiodiketopiperazine (ETP) natural products

Minghao Feng
, Xuefeng Jiang^*

^*此作品的通讯作者

化学与分子工程学院

East China Normal University
Nankai University

科研成果: 期刊稿件 › 文章 › 同行评审

35 引用（Scopus）

摘要

An asymmetric synthetic strategy for constructing the divergent-synthesis monomer of epidithiodiketopiperazine (ETP) natural products has been successfully developed. The functionalized 2,3,3a,4,7,7a-hexahydroindole scaffold was constructed by a diastereoselective inverse electron-demand Diels–Alder (IEDDA) reaction.

源语言	英语
页（从-至）	9690-9692
页数	3
期刊	Chemical Communications
卷	50
期	68
DOI	https://doi.org/10.1039/c4cc04148h
出版状态	已出版 - 29 7月 2014

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10.1039/c4cc04148h

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abstract = "An asymmetric synthetic strategy for constructing the divergent-synthesis monomer of epidithiodiketopiperazine (ETP) natural products has been successfully developed. The functionalized 2,3,3a,4,7,7a-hexahydroindole scaffold was constructed by a diastereoselective inverse electron-demand Diels–Alder (IEDDA) reaction.",

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AB - An asymmetric synthetic strategy for constructing the divergent-synthesis monomer of epidithiodiketopiperazine (ETP) natural products has been successfully developed. The functionalized 2,3,3a,4,7,7a-hexahydroindole scaffold was constructed by a diastereoselective inverse electron-demand Diels–Alder (IEDDA) reaction.

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Stereoselective construction of a key hydroindole precursor of epidithiodiketopiperazine (ETP) natural products

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