batzelladine-d has been researched along with pyrrolidine* in 1 studies
1 other study(ies) available for batzelladine-d and pyrrolidine
Article | Year |
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Total synthesis of batzelladine D.
[structure: see text] Stereoselective total synthesis of batzelladine D was accomplished in 15 steps. This synthesis features (i) successive 1,3-dipolar cycloaddition reactions to form the 2,5-disubstituted pyrrolidine ring system, (ii) esterification of the side chain to the bicyclic guanidine carboxylate, a common synthetic intermediate of batzelladine alkaloids, and (iii) tricyclic guanidine formation under the Mitsunobu reaction conditions. Topics: Alkaloids; Animals; Esterification; Guanidine; Porifera; Pyrimidines; Pyrrolidines; Stereoisomerism | 2002 |