Abstract
Ring-closing metathesis (RCM) reaction of enynes tethered by an N-O bond produced 6- to 8-membered 1,2-oxaza heterocyclic compounds in high yields. Diels-Alder reaction of the cyclic 1,3-dienes with various dienophiles afforded bi- or tri-cyclic compounds efficiently.
| Original language | English |
|---|---|
| Pages (from-to) | 2017-2020 |
| Number of pages | 4 |
| Journal | Synlett |
| Issue number | 13 |
| DOIs | |
| Publication status | Published - 2003 Jan 1 |
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All Science Journal Classification (ASJC) codes
- Organic Chemistry
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Ring-Closing Metathesis of Enynes Tethered by an N-O Bond : Synthesis of 1,2-Oxaza Polycycles by Diels-Alder Reaction of the Ring-Closing Metathesis Products. / Yang, Young Keun; Tae, Jinsung.
In: Synlett, No. 13, 01.01.2003, p. 2017-2020.Research output: Contribution to journal › Article
TY - JOUR
T1 - Ring-Closing Metathesis of Enynes Tethered by an N-O Bond
T2 - Synthesis of 1,2-Oxaza Polycycles by Diels-Alder Reaction of the Ring-Closing Metathesis Products
AU - Yang, Young Keun
AU - Tae, Jinsung
PY - 2003/1/1
Y1 - 2003/1/1
N2 - Ring-closing metathesis (RCM) reaction of enynes tethered by an N-O bond produced 6- to 8-membered 1,2-oxaza heterocyclic compounds in high yields. Diels-Alder reaction of the cyclic 1,3-dienes with various dienophiles afforded bi- or tri-cyclic compounds efficiently.
AB - Ring-closing metathesis (RCM) reaction of enynes tethered by an N-O bond produced 6- to 8-membered 1,2-oxaza heterocyclic compounds in high yields. Diels-Alder reaction of the cyclic 1,3-dienes with various dienophiles afforded bi- or tri-cyclic compounds efficiently.
UR - http://www.scopus.com/inward/record.url?scp=0242351861&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0242351861&partnerID=8YFLogxK
U2 - 10.1055/s-2003-42038
DO - 10.1055/s-2003-42038
M3 - Article
AN - SCOPUS:0242351861
SP - 2017
EP - 2020
JO - Synlett
JF - Synlett
SN - 0936-5214
IS - 13
ER -