Abstract
A diversity-oriented approach to new indolizines highly functionalized at the C3 position was achieved by using the Kabachnik-Fields three-component reaction. Some of the synthesized compounds exhibited a significant gap junction inhibitory activity.
| Original language | English |
|---|---|
| Pages (from-to) | 5759-5768 |
| Number of pages | 10 |
| Journal | Tetrahedron |
| Volume | 73 |
| Issue number | 39 |
| DOIs | |
| Publication status | Published - 2017 Jan 1 |
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All Science Journal Classification (ASJC) codes
- Biochemistry
- Drug Discovery
- Organic Chemistry
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Diversity-oriented functionalization of indolizines at the C3 position via multicomponent Kabachnik-Fields reaction. / Kim, Jinwoo; Heo, Yunkyung; Jung, Youngeun; Lee, Jinu; Kim, Ikyon.
In: Tetrahedron, Vol. 73, No. 39, 01.01.2017, p. 5759-5768.Research output: Contribution to journal › Article
TY - JOUR
T1 - Diversity-oriented functionalization of indolizines at the C3 position via multicomponent Kabachnik-Fields reaction
AU - Kim, Jinwoo
AU - Heo, Yunkyung
AU - Jung, Youngeun
AU - Lee, Jinu
AU - Kim, Ikyon
PY - 2017/1/1
Y1 - 2017/1/1
N2 - A diversity-oriented approach to new indolizines highly functionalized at the C3 position was achieved by using the Kabachnik-Fields three-component reaction. Some of the synthesized compounds exhibited a significant gap junction inhibitory activity.
AB - A diversity-oriented approach to new indolizines highly functionalized at the C3 position was achieved by using the Kabachnik-Fields three-component reaction. Some of the synthesized compounds exhibited a significant gap junction inhibitory activity.
UR - http://www.scopus.com/inward/record.url?scp=85027985887&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85027985887&partnerID=8YFLogxK
U2 - 10.1016/j.tet.2017.08.017
DO - 10.1016/j.tet.2017.08.017
M3 - Article
VL - 73
SP - 5759
EP - 5768
JO - Tetrahedron
JF - Tetrahedron
SN - 0040-4020
IS - 39
ER -