Abstract
A general preparation of new types of benzofurans, benzothiophenes and indoles is realized via chemoselective intramolecular Wittig reactions with the corresponding ester, thioester and amide functionalities using in situ formed phosphorus ylides as key intermediates. The reaction conditions are very mild, and numerous Michael acceptors and commercially available acid chlorides can be applied very efficiently in a one-step procedure.
| Original language | English |
|---|---|
| Pages (from-to) | 8135-8137 |
| Number of pages | 3 |
| Journal | Chemical Communications |
| Volume | 48 |
| Issue number | 65 |
| DOIs | |
| Publication status | Published - 2012 Aug 21 |
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ASJC Scopus subject areas
- Catalysis
- Electronic, Optical and Magnetic Materials
- Ceramics and Composites
- Chemistry(all)
- Surfaces, Coatings and Films
- Metals and Alloys
- Materials Chemistry
Cite this
Preparation of functional benzofurans and indoles via chemoselective intramolecular Wittig reactions. / Lee, Yu Ting; Jang, Yeong Jiunn; Syu, Siang En; Chou, Shu Chi; Lee, Chia Jui; Lin, Wenwei.
In: Chemical Communications, Vol. 48, No. 65, 21.08.2012, p. 8135-8137.Research output: Contribution to journal › Article
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TY - JOUR
T1 - Preparation of functional benzofurans and indoles via chemoselective intramolecular Wittig reactions
AU - Lee, Yu Ting
AU - Jang, Yeong Jiunn
AU - Syu, Siang En
AU - Chou, Shu Chi
AU - Lee, Chia Jui
AU - Lin, Wenwei
PY - 2012/8/21
Y1 - 2012/8/21
N2 - A general preparation of new types of benzofurans, benzothiophenes and indoles is realized via chemoselective intramolecular Wittig reactions with the corresponding ester, thioester and amide functionalities using in situ formed phosphorus ylides as key intermediates. The reaction conditions are very mild, and numerous Michael acceptors and commercially available acid chlorides can be applied very efficiently in a one-step procedure.
AB - A general preparation of new types of benzofurans, benzothiophenes and indoles is realized via chemoselective intramolecular Wittig reactions with the corresponding ester, thioester and amide functionalities using in situ formed phosphorus ylides as key intermediates. The reaction conditions are very mild, and numerous Michael acceptors and commercially available acid chlorides can be applied very efficiently in a one-step procedure.
UR - http://www.scopus.com/inward/record.url?scp=84864198941&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84864198941&partnerID=8YFLogxK
U2 - 10.1039/c2cc33972b
DO - 10.1039/c2cc33972b
M3 - Article
C2 - 22772041
AN - SCOPUS:84864198941
VL - 48
SP - 8135
EP - 8137
JO - Chemical Communications
JF - Chemical Communications
SN - 1359-7345
IS - 65
ER -