122872-03-1

Basic information

• Product Name: 2-Desoxy-4-epi-pulchellin
• Synonyms: 2-Desoxy-4-epi-pulchellin;2,6-Dideacetoxybritanin
• CAS NO: 122872-03-1
• Molecular Formula: C15H22O3
• Molecular Weight: 250.33338
• Product Categories: Sesquiterpenoids
• Mol File: 122872-03-1.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Desoxy-4-epi-pulchellin(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Desoxy-4-epi-pulchellin(122872-03-1)
• EPA Substance Registry System: 2-Desoxy-4-epi-pulchellin(122872-03-1)

Safety Data

• Hazardous Substances Data: 122872-03-1(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
2-Desoxy-4-epi-pulchellin is used as a potential antiviral agent for its ability to combat viral infections, offering a new avenue for treatment and prevention of viral diseases.
2-Desoxy-4-epi-pulchellin is used as an anti-tumor agent for its potential to inhibit tumor growth, making it a candidate for cancer therapy and management.
2-Desoxy-4-epi-pulchellin is used as an anti-inflammatory agent for its capacity to reduce inflammation, which could be beneficial in treating a range of inflammatory conditions.
2-Desoxy-4-epi-pulchellin is used as an analgesic agent for its pain-relieving properties, providing an alternative for pain management in various clinical scenarios.

Upstream product

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Downstream Products

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Relevant articles and documents

Total Synthesis of the Pseudoguaianolide (+)-Confertin

The first total synthesis of the pseudoguaianolide (+)-confertin (1) begins with the preparation of the enantiomerically pure cyclopropane derivative 6b and its stereospecific ring expansion furnishing the five-membered ring A-building block 8a.The AB ketone 21d is produced by intermolecular Michael addition, Lewis acid catalyzed intramolecular hetero-ene reaction, and a pair of oxidation/reduction reactions.Fusion of the heterocyclic five-membered ring and α-methylenation of the ABC intermediate 35c is accomplished by well-known technology.The structure of essential synthetic intermediates has been determined by 2D-NMR, CD spectroscopy, or single crystal X-ray analysis.The whole synthesis starts from α-chloroacetone and reaches the target compound 1 after 22 steps.