A 16-Step Total Synthesis of Norzoanthamine

Abstract Herein, we present a 16-step synthetic route to norzoanthamine that features three pivotal photochemical transformations. A photoinduced dearomative 6π-desymmetrization is employed to access the ABC tricyclic core structure. To address the challenge of constructing the C9–C22 vicinal all-carbon quaternary stereocenters, [2+2]-photocycloaddition, visible-light-induced decarboxylative borylation, and a retro-aldol reaction are strategically employed. The assembly of the norzoanthamine core framework is achieved through a one-pot cascade transformation, combining global deprotection, biomimetic cyclization, and epimerization at C21, resulting in an efficient and concise synthesis of norzoanthamine. 1 Introduction 2 Total Synthesis of Norzoanthamine 3 Conclusion

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Publication Details

Journal
Synlett
Published
2025-04-09
DOI
https://doi.org/10.1055/s-0043-1773532
Primary Topic
Chemical synthesis and alkaloids
Type
article
Field-Weighted Citation Impact
0.00

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article

A 16-Step Total Synthesis of Norzoanthamine

Weiyue Zhang, Yuchen Sun, Yu Sun, Xiao Zhang
Synlett
Chemical synthesis and alkaloids
article

A 16-Step Total Synthesis of Norzoanthamine

Weiyue Zhang, Yuchen Sun, Yu Sun, Xiao Zhang
article en

Abstract

Abstract Herein, we present a 16-step synthetic route to norzoanthamine that features three pivotal photochemical transformations. A photoinduced dearomative 6π-desymmetrization is employed to access the ABC tricyclic core structure. To address the challenge of constructing the C9–C22 vicinal all-carbon quaternary stereocenters, [2+2]-photocycloaddition, visible-light-induced decarboxylative borylation, and a retro-aldol reaction are strategically employed. The assembly of the norzoanthamine core framework is achieved through a one-pot cascade transformation, combining global deprotection, biomimetic cyclization, and epimerization at C21, resulting in an efficient and concise synthesis of norzoanthamine. 1 Introduction 2 Total Synthesis of Norzoanthamine 3 Conclusion

SynlettVol. 36(14)
National Natural Science Foundation of China
Openalex Percentile: Top 95%
Chemical synthesis and alkaloids
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