Sulfur Ylide-Mediated Cascade Transformations to Access Cyclopropylallocolchicinoids with Potent Antimitotic Activity

-rich dibenzocycloheptanes, including enantiomerically enriched variants. Furthermore, we have demonstrated the synthetic utility of this protocol in preparing various advanced intermediates pertinent to natural product synthesis and medicinal chemistry. Comprehensive biological studies have identified a potent analogue that disrupts microtubule organization and dynamics, leading to mitotic arrest and the consequent attenuation of influenza A virus infection.

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Publication Details

Journal
JACS Au
Published
2026-04-11
DOI
https://doi.org/10.1021/jacsau.6c00268
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

Sulfur Ylide-Mediated Cascade Transformations to Access Cyclopropylallocolchicinoids with Potent Antimitotic Activity

Tejal Pathak, Dipto Mukhopadhyay, Kaushalendra Patel, Indranil Banerjee et al.
JACS Au
Cyclopropane Reaction Mechanisms
article

Sulfur Ylide-Mediated Cascade Transformations to Access Cyclopropylallocolchicinoids with Potent Antimitotic Activity

Tejal Pathak, Dipto Mukhopadhyay, Kaushalendra Patel, Indranil Banerjee, Anwita Chattopadhyay, Sripada S. V. Ramasastry, S. C. Pal
article en

Abstract

-rich dibenzocycloheptanes, including enantiomerically enriched variants. Furthermore, we have demonstrated the synthetic utility of this protocol in preparing various advanced intermediates pertinent to natural product synthesis and medicinal chemistry. Comprehensive biological studies have identified a potent analogue that disrupts microtubule organization and dynamics, leading to mitotic arrest and the consequent attenuation of influenza A virus infection.

JACS AuVol. 6(4)
Indian Institute of Science Education and Research Mohali (IN)
Department of Biotechnology, Ministry of Science and Technology, India, Indian Council of Medical Research, Indian Institute of Science Education and Research Mohali
Openalex Percentile: Top 28%
Cyclopropane Reaction Mechanisms
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