
TY  - JOUR
A1  - Banwell, Martin G. 
A1  - Hockless, David C. R. 
A1  - Flynn, Bernard L. 
A1  - Longmore, Robert W. 
A1  - Rae, David 
T1  - Assessment of Double-Barrelled Heck Cyclizations as a Means for Construction of the 14-Phenyl-8,9-dihydro- 6<emph type="2">H</emph>-[1]benzopyrano[4&#8242;,3&#8242;:4,5]pyrrolo[2,1-<emph type="2">a</emph>]isoquinolin- 6-one Core Associated with Certain Members of the Lamellarin Class  of Marine Natural Product
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1999
VL  - 52
IS  - 8
SP  - 755
EP  - 766
KW  - 
UR  - https://doi.org/10.1071/CH99021 
N2  - The 1,2,4-trisubstituted pyrrole (4), which is readily prepared from pyrrole itself, undergoes double- barrelled 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. 
ER  -

