Bronsted acid mediated Z-selective synthesis of phenylethylidene indoles from 3-diazooxindoles

1. A metal free TfOH-catalyzed alkylation of styrenes with 3-diazooxindoles was described. A library of 3-aryloxindoles can be synthesized in good yields and with high stereoselectivitie. 2. The structure of product was confirmed by NMR Spectra and Mass Spectroscope. [1st Award]

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Main Author: Wang, Xinzhu
Other Authors: Zaher Judeh
Format: Student Research Poster
Language:English
Published: Nanyang Technological University 2021
Subjects:
Online Access:https://hdl.handle.net/10356/151822
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Institution: Nanyang Technological University
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spelling sg-ntu-dr.10356-1518222021-07-04T20:11:03Z Bronsted acid mediated Z-selective synthesis of phenylethylidene indoles from 3-diazooxindoles Wang, Xinzhu Zaher Judeh School of Chemical and Biomedical Engineering Tatina Madhu Babu Zaher@ntu.edu.sg Engineering::Bioengineering 1. A metal free TfOH-catalyzed alkylation of styrenes with 3-diazooxindoles was described. A library of 3-aryloxindoles can be synthesized in good yields and with high stereoselectivitie. 2. The structure of product was confirmed by NMR Spectra and Mass Spectroscope. [1st Award] 2021-07-02T06:55:38Z 2021-07-02T06:55:38Z 2019 Student Research Poster Wang, X. (2019). Bronsted acid mediated Z-selective synthesis of phenylethylidene indoles from 3-diazooxindoles. Student Research Poster, Nanyang Technological University, Singapore. https://hdl.handle.net/10356/151822 https://hdl.handle.net/10356/151822 en SCBE18025 © 2019 The Author(s). application/pdf Nanyang Technological University
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering::Bioengineering
spellingShingle Engineering::Bioengineering
Wang, Xinzhu
Bronsted acid mediated Z-selective synthesis of phenylethylidene indoles from 3-diazooxindoles
description 1. A metal free TfOH-catalyzed alkylation of styrenes with 3-diazooxindoles was described. A library of 3-aryloxindoles can be synthesized in good yields and with high stereoselectivitie. 2. The structure of product was confirmed by NMR Spectra and Mass Spectroscope. [1st Award]
author2 Zaher Judeh
author_facet Zaher Judeh
Wang, Xinzhu
format Student Research Poster
author Wang, Xinzhu
author_sort Wang, Xinzhu
title Bronsted acid mediated Z-selective synthesis of phenylethylidene indoles from 3-diazooxindoles
title_short Bronsted acid mediated Z-selective synthesis of phenylethylidene indoles from 3-diazooxindoles
title_full Bronsted acid mediated Z-selective synthesis of phenylethylidene indoles from 3-diazooxindoles
title_fullStr Bronsted acid mediated Z-selective synthesis of phenylethylidene indoles from 3-diazooxindoles
title_full_unstemmed Bronsted acid mediated Z-selective synthesis of phenylethylidene indoles from 3-diazooxindoles
title_sort bronsted acid mediated z-selective synthesis of phenylethylidene indoles from 3-diazooxindoles
publisher Nanyang Technological University
publishDate 2021
url https://hdl.handle.net/10356/151822
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