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Showing papers by "Avijit Banerji published in 1976"


Journal ArticleDOI
TL;DR: In this article, a new alkaloid, rhazinaline, has been characterised as 16-formyl-16-epistrictamine and a detailed spectroscopical study of geissoschizine, which had not been previously isolated from a plant source, was carried out confirming the previous structural assignment.
Abstract: Chemical investigation of the basic principles of the leaves of Rhazya stricta Decaisne led to the isolation of a number of indolic bases. The studies on two of these, viz., rhazinaline and geissoschizine are described. Rhazinaline, a new alkaloid, has been characterised as 16-formyl-16-epistrictamine. A detailed spectroscopical study of geissoschizine, which had not been previously isolated from a plant source, was carried out confirming the previous structural assignment. The isolation of this alkaloid from a plant source is important from a biogenetic viewpoint, since geissoschizine is one of the key preformed intermediates in the biosynthesis of C19–C20 indole alkaloids.

14 citations




Journal ArticleDOI
TL;DR: In this paper, a new alkaloid named rhazinaline has been characterised as 16-formyl-16-epistrictamine and a detailed spectroscopical study of geissoschizine, which had not been previously isolated from a plant source, was carried out confirming the previous structural assignment.
Abstract: Chemical investigation of the basic principles of the leaves of Rhazya stricta Decaisne led to the isolation of a number of indolic bases. The studies on two of these, viz., rhazinaline and geissoschizine are described. Rhazinaline, a new alkaloid, has been characterised as 16-formyl-16-epistrictamine. A detailed spectroscopical study of geissoschizine, which had not been previously isolated from a plant source, was carried out confirming the previous structural assignment. The isolation of this alkaloid from a plant source is important from a biogenetic viewpoint, since geissoschizine is one of the key preformed intermediates in the biosynthesis of C 19 -C 20 indole alkaloids.

1 citations