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Annulation of para-Quinone Methides through 1,6-Nucleophilic Conjugate Addition: A simple Approach for Complex Molecular scaffolds of Biological significance

Implementing Organization

Principal Investigator
Prof. suresh Babasaheb Waghmode
savitribai Phule Pune University, Maharashtra

Project Overview

The aim of this proposal is to develop pharmaceutically important spirocyclic molecules (1,4-dioxa, furane, pyrane-cyclohexanone), by [4+2] and [3+2] annulation through 1,6 conjugate addition of para- quinone methide with various nuclephiles or electrophiles (diol and halohydrin). These molecules are drugs and drug like properties. This proposed work envisioned to synthesize indane and carbocyclic compounds synthesis through [4+1] cyclyzation over novel type of Pd catalysed cross coupling of cyclopropanols with 2-Br-p-QMs followed by 1,6-conjugate addition reaction. Finally, VLPC studies of the p-QMs will be utilized for sunlight harvesting and related green, sustainable construction of complex molecular scaffolds. The bio-activity of these novel synthesized compounds will be carried out. Furthermore the synthetic scope of these methods will be extensively explored.

Source

Source
Anusandhan National Research Foundation/science and Engineering Research Board (sERB), DsT 2023-24
Funding Organization
Quick Information
Area of Research
Chemical Sciences
Start Date
2023
End Date
2026
Status
Ongoing
Contact
suresh.waghmode@gmail.com
Output
No. of Research Paper
00
Technologies (If Any)
00
No. of PhD Produced
00
Publications
00
No. of Patents
Filed : 00
Grant : 00
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