TY - JOUR
T1 - Assessment of double-barrelled heck cyclizations as a means for construction of the 14-Phenyl-8,9-dihydro6H-[1]benzopyrano[4′,3′:4,5]pyrrolo[2,1-a] isoquinolin-6-one core associated with certain members of the lamellarin class of marine natural product
AU - Banwell, Martin G.
AU - Flynn, Bernard L.
AU - Hockless, David C.R.
AU - Longmore, Robert W.
AU - David Rae, A.
PY - 1999/12/1
Y1 - 1999/12/1
N2 - The 1,2,4-trisubstituted pyrrole (4), which is readily prepared from pyrrole itself, undergoes doublebarrelled Heck cyclizations to give, inter alia, compounds (3) and (17) for which crystal structures have been determined. Product (3) constitutes the core associated with several key members, e.g. (1) and (2), of the lamellarin class of marine alkaloid.
AB - The 1,2,4-trisubstituted pyrrole (4), which is readily prepared from pyrrole itself, undergoes doublebarrelled Heck cyclizations to give, inter alia, compounds (3) and (17) for which crystal structures have been determined. Product (3) constitutes the core associated with several key members, e.g. (1) and (2), of the lamellarin class of marine alkaloid.
UR - http://www.scopus.com/inward/record.url?scp=4243055264&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:4243055264
SN - 0004-9425
VL - 52
JO - Australian Journal of Chemistry
JF - Australian Journal of Chemistry
IS - 8
ER -