Skip navigation
Please use this identifier to cite or link to this item: http://arks.princeton.edu/ark:/88435/dsp01t148fh33k
Title: Further Progress Towards the Total Synthesis of Paecilospirone
Authors: Chung, Victoria
Advisors: Doyle, Abigail
Department: Chemistry
Class Year: 2014
Abstract: The [5,6]-bisbenzannulated spiroacetal paecilospirone possesses a challenging scaffold that contains the unique spiroacetal structure, and is a viable drug target for its antimitotic properties. This thesis details progress towards a concise, modular synthesis that implements the nickel-catalyzed Suzuki cross-coupling of the ethoxy chromene and arylboronic acid precursors, a reaction which enables late-stage functionalization of the molecular scaffold. Also featured is a DDQ-mediated oxidative spiroacetalization, a method amenable to catalytic asymmetric induction. Initial optimization efforts of the two major low-yielding steps, the construction of 2H-Chromene and the spiroacetal moiety, are discussed. Additionally, we report the mischaracterization of a critical intermediate generated by a NBS halobromination reaction previously published by the Doyle lab. This has prompted a reevaluation of the proposed synthetic route and investigations concerning the revised pathway.
Extent: 92 pages
URI: http://arks.princeton.edu/ark:/88435/dsp01t148fh33k
Type of Material: Princeton University Senior Theses
Language: en_US
Appears in Collections:Chemistry, 1926-2016

Files in This Item:
File SizeFormat 
Chung_Victoria.pdf3.31 MBAdobe PDF    Request a copy


Items in Dataspace are protected by copyright, with all rights reserved, unless otherwise indicated.