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^*

^*Corresponding author for this work

School of Chemistry and Molecular Engineering

East China Normal University
Nankai University

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

35 Scopus citations

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.

Original language	English
Pages (from-to)	9690-9692
Number of pages	3
Journal	Chemical Communications
Volume	50
Issue number	68
DOIs	https://doi.org/10.1039/c4cc04148h
State	Published - 29 Jul 2014

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title = "Stereoselective construction of a key hydroindole precursor of epidithiodiketopiperazine (ETP) natural products",

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.",

author = "Minghao Feng and Xuefeng Jiang",

year = "2014",

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day = "29",

doi = "10.1039/c4cc04148h",

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AU - Feng, Minghao

AU - Jiang, Xuefeng

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Y1 - 2014/7/29

N2 - 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.

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.

UR - https://www.scopus.com/pages/publications/84905046758

U2 - 10.1039/c4cc04148h

DO - 10.1039/c4cc04148h

M3 - 文章

C2 - 25017898

AN - SCOPUS:84905046758

SN - 1359-7345

VL - 50

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EP - 9692

JO - Chemical Communications

JF - Chemical Communications

IS - 68

ER -

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

Abstract

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