Synthesis of podophyllotoxin and its derivatives via nicl2/nabh4 reduction of isoxazoline ring

Suresh Babu, M. and Rai, K. M. Lokanatha (2013) Synthesis of podophyllotoxin and its derivatives via nicl2/nabh4 reduction of isoxazoline ring. Asian Journal of Chemistry, 25 (17). pp. 9555-9557.

[img] Text (Full Text)
Che_2013_Lokanatha Rai_01.pdf - Published Version
Restricted to Registered users only
Download (245kB) | Request a copy
Official URL: http://doi.org/10.14233/ajchem.2013.15073

Abstract

A novel synthesis of podophyllotoxin was carried out in four steps. The key step was reduction of isoxazoline ring followed by diazotization and the resultant alkene was treated with Mn(OAc)3/CH3COOK to form podophyllotoxin.

Item Type: Article
Subjects: C Chemical Science > Chemistry
Divisions: Department of > Chemistry
Depositing User: Arshiya Kousar Library Assistant
Date Deposited: 03 Oct 2019 05:39
Last Modified: 13 Jan 2023 11:16
URI: http://eprints.uni-mysore.ac.in/id/eprint/7928

Actions (login required)

View Item View Item
uomeprints is powered by EPrints 3 which is developed by the School of Electronics and Computer Science at the University of Southampton. More information and software credits.