Abstract
The Pd-catalyzed reaction of internal alkynes with tethered amino groups in the presence of PhCO2H and RENORPHOS as chiral phosphine ligand is reported. Various five- and six-membered nitrogen-containing heterocycles were obtained in good to high yield with moderate to high ee.
| Original language | English |
|---|---|
| Pages (from-to) | 1622-1623 |
| Number of pages | 2 |
| Journal | Journal of the American Chemical Society |
| Volume | 126 |
| Issue number | 6 |
| Publication status | Published - Feb 18 2004 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Chemistry(all)
Cite this
Palladium-Catalyzed Intramolecular Asymmetric Hydroamination of Alkynes. / Lutete, Léopold M.; Kadota, Isao; Yamamoto, Yoshinori.
In: Journal of the American Chemical Society, Vol. 126, No. 6, 18.02.2004, p. 1622-1623.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Palladium-Catalyzed Intramolecular Asymmetric Hydroamination of Alkynes
AU - Lutete, Léopold M.
AU - Kadota, Isao
AU - Yamamoto, Yoshinori
PY - 2004/2/18
Y1 - 2004/2/18
N2 - The Pd-catalyzed reaction of internal alkynes with tethered amino groups in the presence of PhCO2H and RENORPHOS as chiral phosphine ligand is reported. Various five- and six-membered nitrogen-containing heterocycles were obtained in good to high yield with moderate to high ee.
AB - The Pd-catalyzed reaction of internal alkynes with tethered amino groups in the presence of PhCO2H and RENORPHOS as chiral phosphine ligand is reported. Various five- and six-membered nitrogen-containing heterocycles were obtained in good to high yield with moderate to high ee.
UR - http://www.scopus.com/inward/record.url?scp=1242291816&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=1242291816&partnerID=8YFLogxK
M3 - Article
C2 - 14871079
AN - SCOPUS:1242291816
VL - 126
SP - 1622
EP - 1623
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
SN - 0002-7863
IS - 6
ER -