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
N1 - Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 2003
Y1 - 2003
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 -