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]
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 |
Similar Items
-
Product Selectivity Control in the Brønsted Acid-Mediated Reactions with 2-Alkynylanilines
by: Valerio Morlacci, et al.
Published: (2024-08-01) -
NHC-catalyzed [12+2] reaction of polycyclic arylaldehydes for access to indole derivatives
by: Ji, Hong, et al.
Published: (2023) -
Impact of malonate on the metabolism and fatty acid synthesis of genetically engineered saccharomyces cerevisiae
by: Tan, Kee Yang
Published: (2015) -
Profiling the biocontrol agents, nitrogen-fixing bacteria, and indole acetic acid-producing bacteria in anthill soil
by: Emmanuel E. Imade, et al.
Published: (2024-09-01) -
Brønsted acid catalyzed hydroamination and its application to total synthesis of cuspareine
by: Bay, Siew Ting
Published: (2010)