Link to the University of Pittsburgh Homepage
Link to the University Library System Homepage Link to the Contact Us Form

TOTAL SYNTHESIS OF PUREALIN AND ITS ANALOGUESSYNTHESIS OF LAGUNAPYRONE B AND ITS ISOMERS WITH FLUOROUS MIXTURE SYNTHESIS

Yang, Fanglong (2006) TOTAL SYNTHESIS OF PUREALIN AND ITS ANALOGUESSYNTHESIS OF LAGUNAPYRONE B AND ITS ISOMERS WITH FLUOROUS MIXTURE SYNTHESIS. Doctoral Dissertation, University of Pittsburgh. (Unpublished)

[img]
Preview
PDF
Primary Text

Download (1MB) | Preview

Abstract

Purealin is a natural product that has been isolated from the sea sponge Psammaplysilla purea known to inhibit axonemal dynein. A total synthesis of purealin and a small library of purealin analogues are reported here in. This research allows initial examination of biological properties of purealin and its analogues. The results indicate purealin and some of the analogues inhibited the ATPase activity of isolated cytoplasmic dynein heavy chain. The inhibitory effect of purealin was concentration-dependent. The library of puealidin A showed effective antiproliferative activity against a mouse leukemia cell line, but selective activities against human carcinoma cell lines. These data illustrate small molecule inhibitors of cytoplasmic dynein that could prove to be useful tools for investigation of the cellular function of cytoplasmic dynein.Lagunapyrone B, a marine bacteria isolated by Fenical in 1996, possesses an unusual alpha-pyrone functionalized with highly methyl-branched side chain, a conjugated diene and two skipped dienes. The carbon skeleton of lagunapyrones has not been previously observed. Because of the long distance between the two groups of stereocenters, the absolute configuration of these compounds is difficult to assign using spectroscopic methods. Using fluorous mixture synthesis (FMS), we have synthesized four diastereomers in order to determine the absolute configuration of the natural product. By comparing the [¦Á]D25 data of final four isomers, compound 2.1c was determined to be the natural product, whose configuration is 6R, 7S, 19S, 20S, 21R.


Share

Citation/Export:
Social Networking:
Share |

Details

Item Type: University of Pittsburgh ETD
Status: Unpublished
Creators/Authors:
CreatorsEmailPitt UsernameORCID
Yang, Fanglongfly1@pitt.eduFLY1
ETD Committee:
TitleMemberEmail AddressPitt UsernameORCID
Committee ChairCurran, Denniscurran@pitt.eduCURRAN
Committee MemberDay, Billybday@pitt.eduBDAY
Committee MemberSchafmeister, Chrismeister@pitt.eduMEISTER
Committee MemberWilcox, Craigdaylite@pitt.eduDAYLITE
Date: 24 October 2006
Date Type: Completion
Defense Date: 23 June 2006
Approval Date: 24 October 2006
Submission Date: 6 June 2006
Access Restriction: No restriction; Release the ETD for access worldwide immediately.
Institution: University of Pittsburgh
Schools and Programs: Dietrich School of Arts and Sciences > Chemistry
Degree: PhD - Doctor of Philosophy
Thesis Type: Doctoral Dissertation
Refereed: Yes
Uncontrolled Keywords: lagunapyrone; mixture synthesis; purealin
Other ID: http://etd.library.pitt.edu/ETD/available/etd-06062006-184213/, etd-06062006-184213
Date Deposited: 10 Nov 2011 19:46
Last Modified: 15 Nov 2016 13:44
URI: http://d-scholarship.pitt.edu/id/eprint/8021

Metrics

Monthly Views for the past 3 years

Plum Analytics


Actions (login required)

View Item View Item