NHC-Catalyzed Umpolung Driven Intramolecular Cyclizations for the Generation of 3,4-Cycloheptanone Annulated Tetracyclic Indole Derivatives

In this Letter, we disclose the development and exploitation of umpolung reactivity of N-heterocyclic carbene (NHC) organocatalysts in generating tetracyclic indole derivatives with the introduction of a cycloheptane ring forming event. The NHC-catalyzed intramolecular vinylogous Stetter, Stetter, benzoin, and formal cross-dehydrogenative coupling transformations have been executed, enabling the construction of 3,4-cycloheptannulated indole derivatives in good to excellent yields. The developed protocols utilize an inexpensive catalyst and feature operational simplicity, atom economy, gram-scale syntheses, and postsynthetic availability.

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Publication Details

Journal
Organic Letters
Published
2024-10-07
DOI
https://doi.org/10.1021/acs.orglett.4c02640
Citations
9
Primary Topic
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
Type
article
Field-Weighted Citation Impact
2.25

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article

NHC-Catalyzed Umpolung Driven Intramolecular Cyclizations for the Generation of 3,4-Cycloheptanone Annulated Tetracyclic Indole Derivatives

Jagadeesh Babu Nanubolu, Surisetti Suresh, Purna Chandra Behera, Bandari Anilkumar
9 citations
Organic Letters
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
2.25
article

NHC-Catalyzed Umpolung Driven Intramolecular Cyclizations for the Generation of 3,4-Cycloheptanone Annulated Tetracyclic Indole Derivatives

Jagadeesh Babu Nanubolu, Surisetti Suresh, Purna Chandra Behera, Bandari Anilkumar
article en
9 citations

Abstract

In this Letter, we disclose the development and exploitation of umpolung reactivity of N-heterocyclic carbene (NHC) organocatalysts in generating tetracyclic indole derivatives with the introduction of a cycloheptane ring forming event. The NHC-catalyzed intramolecular vinylogous Stetter, Stetter, benzoin, and formal cross-dehydrogenative coupling transformations have been executed, enabling the construction of 3,4-cycloheptannulated indole derivatives in good to excellent yields. The developed protocols utilize an inexpensive catalyst and feature operational simplicity, atom economy, gram-scale syntheses, and postsynthetic availability.

Organic LettersVol. 26(41)
Indian Institute of Chemical Technology (IN), Academy of Scientific and Innovative Research (IN)
University Grants Commission, Science and Engineering Research Board
Openalex Percentile: Top 12%
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
2.25
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NHC-Catalyzed Umpolung Driven Intramolecular Cyclizations for the Generation of 3,4-Cycloheptanone Annulated Tetracyclic Indole Derivatives — Jagadeesh Babu Nanubolu, Surisetti Suresh, et al. · Organic Letters (2024) | TGRS Research Map | TGRS