Abstract
By simply stirring in water, organic azides and terminal alkynes are readily and cleanly converted into 1,4-disubstituted 1,2,3-triazoles through a highly efficient and regioselective copper(I)-catalyzed process (see scheme for an example).
| Original language | English |
|---|---|
| Pages (from-to) | 2596-2599 |
| Number of pages | 4 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 41 |
| Issue number | 14 |
| DOIs | |
| Publication status | Published - 15 Jul 2002 |
| Externally published | Yes |
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Keywords
- Azides
- Copper
- Cycloaddition
- Homogeneous catalysis
- Nitrogen heterocycles
ASJC Scopus subject areas
- Chemistry(all)
Cite this
A stepwise huisgen cycloaddition process : Copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes. / Rostovtsev, Vsevolod V.; Green, Luke G.; Fokin, Valery V.; Sharpless, K. Barry.
In: Angewandte Chemie - International Edition, Vol. 41, No. 14, 15.07.2002, p. 2596-2599.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - A stepwise huisgen cycloaddition process
T2 - Copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes
AU - Rostovtsev, Vsevolod V.
AU - Green, Luke G.
AU - Fokin, Valery V.
AU - Sharpless, K. Barry
PY - 2002/7/15
Y1 - 2002/7/15
N2 - By simply stirring in water, organic azides and terminal alkynes are readily and cleanly converted into 1,4-disubstituted 1,2,3-triazoles through a highly efficient and regioselective copper(I)-catalyzed process (see scheme for an example).
AB - By simply stirring in water, organic azides and terminal alkynes are readily and cleanly converted into 1,4-disubstituted 1,2,3-triazoles through a highly efficient and regioselective copper(I)-catalyzed process (see scheme for an example).
KW - Azides
KW - Copper
KW - Cycloaddition
KW - Homogeneous catalysis
KW - Nitrogen heterocycles
UR - http://www.scopus.com/inward/record.url?scp=0037099395&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0037099395&partnerID=8YFLogxK
U2 - 10.1002/1521-3773(20020715)41:14<2596::AID-ANIE2596>3.0.CO;2-4
DO - 10.1002/1521-3773(20020715)41:14<2596::AID-ANIE2596>3.0.CO;2-4
M3 - Article
VL - 41
SP - 2596
EP - 2599
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
SN - 1433-7851
IS - 14
ER -