Covering: 2009 to 2022 The Stemona alkaloids, which are found in plant species from the
family Stemonaceae, represent a tremendously large and structurally-diverse family of …

Transannular reactions have shown a remarkable performance for the construction of
polycyclic scaffolds from medium-or large-sized cyclic molecules in an unconventional …

Efficient chemical synthesis is critical to satisfying future demands for medicines, materials,
and agrochemicals. Retrosynthetic analysis of modestly complex molecules has been …

The first total syntheses of bisdehydrotuberostemonine D (8) and putative
bisdehydrotuberostemonine E (9), two novel pyrrole Stemona alkaloids, along with the …

The asymmetric total syntheses of five pyrrole-type Stemona alkaloids and two
stereoisomers were accomplished, among which 3-n-butylneostemonine and …

Six Stemona alkaloids were synthesized racemically using stemoamide, obtained via a
cascade cyclization or our reported transannular cyclization of parvistemoamide, as the …

The structural revision of four Stemona alkaloids from Stemona tuberosa is reported. The
misassignment of the tuberostemonine O structure (1) was recognized when a new alkaloid …

In recent years, researches on the total syntheses of Stemona alkaloids with different 5/7
bicyclic systems have attracted increasing attention, and the development momentum in this …

Our research group has been exploring a lactam strategy for the concise total synthesis of
complex alkaloids. In this article, we report full details of the unified total synthesis of …

The natural product parvistemoamide was isolated in 1991 and has ostensibly eluded
synthesis. Its distinctive assigned structure represents the first and only Stemona alkaloid …