2002
First total syntheses of dihydroflustramine C and flustramine E, alkaloids from the marine bryozoan Flustra foliacea. Morales-Ríos Martha S., Suárez-Castillo Oscar R., Joseph-Nathan P. DOI: http://dx.doi.org/10.1016/S0040-4020(02)00011-X
Abstract
We have developed a simple and practical method for providing the common tricyclic skeleton of physostigmine type alkaloids, and demonstrated its utility for indole alkaloid synthesis. Thus, we achieved the firsttotalsyntheses of ()-dihydroflustramine C and ()-flustramine E, as well as the totalsyntheses of their debromoanalogues from the corresponding 2-hydroxyindolenines in five steps with 31, 27, 39 and 23% overall yields, respectively. The structures of some intermediates were confirmed by single crystal X-ray diffraction analyses.
Absolute configuration determination of 2-(2-oxo-3-indolyl)acetamide derivatives
Configuration, stereodynamics and crystal structure of 3-substituted-2-oxofuro[2,3-b]indoles
Cleavage of alkoxycarbonyl protecting groups from carbamates by t-BuNH2
Trapping enols of esters and lactones with diazomethane
Synthesis of 6-bromo-2-arylindoles using 2-iodobenzoic acid as precursor
13C NMR and crystallographic evidence of push-pull effects in furoindolic ?-enamino esters
Total Syntheses of Five Indole Alkaloids from the Marine Bryozoan Flustra foliacea
Synthesis of Bromoindole Alkaloids from Laurencia brongniartii