Abstract
A general preparation of new types of highly functional phosphorus zwitterions is realized via tandem three-component reactions using the corresponding functional alkanes, aldehydes, and Bu 3P. Starting from our novel zwitterions as synthetic reagents with commercially available acid chlorides in a one-step procedure provides an attractive approach toward furo[3,2-c]coumarins.
| Original language | English |
|---|---|
| Pages (from-to) | 1906-1909 |
| Number of pages | 4 |
| Journal | Organic Letters |
| Volume | 14 |
| Issue number | 7 |
| DOIs | |
| Publication status | Published - 2012 Apr 6 |
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ASJC Scopus subject areas
- Organic Chemistry
- Physical and Theoretical Chemistry
- Biochemistry
Cite this
Preparation of functional phosphorus zwitterions from activated alkanes, aldehydes, and tributylphosphine : Synthesis of polysubstituted furo[3,2-c ]coumarins. / Lee, Chia Jui; Jang, Yeong Jiunn; Wu, Zong Ze; Lin, Wenwei.
In: Organic Letters, Vol. 14, No. 7, 06.04.2012, p. 1906-1909.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Preparation of functional phosphorus zwitterions from activated alkanes, aldehydes, and tributylphosphine
T2 - Synthesis of polysubstituted furo[3,2-c ]coumarins
AU - Lee, Chia Jui
AU - Jang, Yeong Jiunn
AU - Wu, Zong Ze
AU - Lin, Wenwei
PY - 2012/4/6
Y1 - 2012/4/6
N2 - A general preparation of new types of highly functional phosphorus zwitterions is realized via tandem three-component reactions using the corresponding functional alkanes, aldehydes, and Bu 3P. Starting from our novel zwitterions as synthetic reagents with commercially available acid chlorides in a one-step procedure provides an attractive approach toward furo[3,2-c]coumarins.
AB - A general preparation of new types of highly functional phosphorus zwitterions is realized via tandem three-component reactions using the corresponding functional alkanes, aldehydes, and Bu 3P. Starting from our novel zwitterions as synthetic reagents with commercially available acid chlorides in a one-step procedure provides an attractive approach toward furo[3,2-c]coumarins.
UR - http://www.scopus.com/inward/record.url?scp=84859600243&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84859600243&partnerID=8YFLogxK
U2 - 10.1021/ol3005479
DO - 10.1021/ol3005479
M3 - Article
VL - 14
SP - 1906
EP - 1909
JO - Organic Letters
JF - Organic Letters
SN - 1523-7060
IS - 7
ER -