Biomimetic synthesis of the pentacyclic alkaloid (.+-.)-nirurine and possible biogenetic rearrangement of a precursor into (.+-.)-norsecurinine
- 1 January 1992
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 114 (1) , 382-383
- https://doi.org/10.1021/ja00027a070
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- Reaction of allylic tin reagents with nitrogen heteroaromatics activated by alkyl chloroformates: regioselective synthesis of .alpha.-allylated 1,2-dihydropyridines and change of the regioselectivity depending on methyl substituents at the allylic moietyThe Journal of Organic Chemistry, 1988
- Intramolecular Cyclizations of Allenic Acylureas and ‐AmidesHelvetica Chimica Acta, 1987
- X-Ray crystal and molecular structure of nirurine, a novel alkaloid related to the securinega alkaloid skeleton, from Phyllanthus niruri(Euphorbiaceae)Journal of the Chemical Society, Perkin Transactions 1, 1985