Ask a Librarian

Threre are lots of ways to contact a librarian. Choose what works best for you.

HOURS TODAY

10:00 am - 3:00 pm

Reference Desk

CONTACT US BY PHONE

(802) 656-2022

Voice

(802) 503-1703

Text

MAKE AN APPOINTMENT OR EMAIL A QUESTION

Schedule an Appointment

Meet with a librarian or subject specialist for in-depth help.

Email a Librarian

Submit a question for reply by e-mail.

WANT TO TALK TO SOMEONE RIGHT AWAY?

Library Hours for Tuesday, April 23rd

All of the hours for today can be found below. We look forward to seeing you in the library.
HOURS TODAY
8:00 am - 12:00 am
MAIN LIBRARY

SEE ALL LIBRARY HOURS
WITHIN HOWE LIBRARY

MapsM-Th by appointment, email govdocs@uvm.edu

Media Services8:00 am - 7:00 pm

Reference Desk10:00 am - 3:00 pm

OTHER DEPARTMENTS

Special Collections10:00 am - 6:00 pm

Dana Health Sciences Library7:30 am - 11:00 pm

 

CATQuest

Search the UVM Libraries' collections

UVM Theses and Dissertations

Browse by Department
Format:
Print
Author:
Cheng, Xiayun
Dept./Program:
Chemistry
Year:
2013
Degree:
PhD
Abstract:
The protecting group-free total syntheses of Lycopodium alkaloids nankakurines A and B have been accomplished in 6 and 7 steps, respectively, via a third Lycopodium alkaloid, luciduline. A 3-step highly stereo- and regioselective total synthesis of the alkaloid, luciduline is outlined. The key steps of this approach consist of a diethylaluminum chloride catalyzed Diels-Alder reaction, reductive amination and subsequent Mannich reaction to form the luciduline tricyclic skeleton. The first full 2D NMR spectral characterization was carried out on luciduline which further confirmed its structure. Using luciduline as a precursor, further aminoallylation, ring-closing metathesis and hydrogenation furnished nankakurine A, which was converted to nankakurine B by reductive methylation.
With the availability of luciduline and its analogs in sufficient quantities, an efficient asymmetric total synthesis of ( - )-Iyconadin C was achieved in 12 steps. This total synthesis features a short preparation of a luciduline congener, a ring expansion reaction and an assembly of a 2-pyridone. Extensive investigations were conducted on the regioselectivity of the ring expansion. The highlight of this synthetic route is the mild pyridone ring formation through a 6 [Pi]-electrocyclization reaction which is unprecedented for non-aryl isocyanates.
A total synthesis of the bridge-fused Aspidosperma indole alkaloid (±) has been accomplished in seven steps starting from the commercially available tryptamine. The bridge-containing scaffold of (±)-subincanadine F was efficiently assembled by a low valent titanium mediated intramolucular nucleophilic acyl substiutution (INAS) reaction. The synthetic utility of titanium-medicated INAS reagents for heterocyclic compounds was further demonstrated.