Total synthesis of enisorine D and its analogues

Shashi, and Khan, Faiz Ahmed (2019) Total synthesis of enisorine D and its analogues. Masters thesis, Indian institute of technology Hyderabad.

[img] Text
MSc_Thesis_TD1345_2019.pdf
Restricted to Repository staff only until 10 May 2020.

Download (2MB) | Request a copy

Abstract

The first total synthesis of enisorine D, an inhibitor of T3SS dependent Yope secretion of Y. pseudotuberculosis isolated from a marine sponge Iotrochota cf. Iota is described in 63.7% overall yield. The target molecule was achieved in seven linear steps from tyramine via simple and effective transformations such as bromination, acylation, alkylation, azidation, reduction and routine acid-amine coupling. A total of sixteen analogues were prepared by coupling with eight different cinnamic acids, two bromopyrrole carboxylic acids and phenyl carboxylic acids.

[error in script]
IITH Creators:
IITH CreatorsORCiD
Khan, Faiz AhmedUNSPECIFIED
Item Type: Thesis (Masters)
Uncontrolled Keywords: Total synthesis,Enisorine-D, Alkylation
Subjects: Chemistry
Divisions: Department of Chemistry
Depositing User: Team Library
Date Deposited: 13 May 2019 07:16
Last Modified: 13 May 2019 07:16
URI: http://raiithold.iith.ac.in/id/eprint/5132
Publisher URL:
Related URLs:

    Actions (login required)

    View Item View Item
    Statistics for RAIITH ePrint 5132 Statistics for this ePrint Item