Expanding the Synthetic Scope of Rawal’s Diene: Access to Pyran and Pyrazole Derivatives

The study demonstrates the synthetic versatility of Rawal's diene as a key reagent for the scalable synthesis of MedChem-relevant building blocks. The hetero-Diels-Alder cycloaddition with various ketones based on this reagent provides efficient one-step access to a wide array of substituted dihydropyranones in a scalable manner. These derivatives have shown high synthetic potential for further transformations to tetrahydropyranones and various pyrazoles with an uncommon substitution pattern. All these results demonstrated the effectiveness of Rawal's diene for the synthesis of diverse pyranone-based building blocks and its potential for industrial applications.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-01-13
DOI
https://doi.org/10.1021/acs.joc.5c02273
Primary Topic
Cyclization and Aryne Chemistry
Type
article
Field-Weighted Citation Impact
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article

Expanding the Synthetic Scope of Rawal’s Diene: Access to Pyran and Pyrazole Derivatives

Oleksii Shamrai, Dmytro Leha, Dmytro M. Volochnyuk, Eugeniy N. Ostapchuk et al.
The Journal of Organic Chemistry
Cyclization and Aryne Chemistry
article

Expanding the Synthetic Scope of Rawal’s Diene: Access to Pyran and Pyrazole Derivatives

Oleksii Shamrai, Dmytro Leha, Dmytro M. Volochnyuk, Eugeniy N. Ostapchuk, Evgenij V. Zarudnitskii, Serhiy V. Ryabukhin
article en

Abstract

The study demonstrates the synthetic versatility of Rawal's diene as a key reagent for the scalable synthesis of MedChem-relevant building blocks. The hetero-Diels-Alder cycloaddition with various ketones based on this reagent provides efficient one-step access to a wide array of substituted dihydropyranones in a scalable manner. These derivatives have shown high synthetic potential for further transformations to tetrahydropyranones and various pyrazoles with an uncommon substitution pattern. All these results demonstrated the effectiveness of Rawal's diene for the synthesis of diverse pyranone-based building blocks and its potential for industrial applications.

The Journal of Organic ChemistryVol. 91(3)
Taras Shevchenko National University of Kyiv (UA), National Technical University of Ukraine “Igor Sikorsky Kyiv Polytechnic Institute” (UA), Institute of Organic Chemistry (UA), Enamine (Ukraine) (UA)
Industry, innovation and infrastructure
Openalex Percentile: Top 91%
Cyclization and Aryne Chemistry
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Expanding the Synthetic Scope of Rawal’s Diene: Access to Pyran and Pyrazole Derivatives — Oleksii Shamrai, Dmytro Leha, et al. · The Journal of Organic Chemistry (2026) | TGRS Research Map | TGRS