Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
2R01CA040081-09A2
Application #
2090105
Study Section
Medicinal Chemistry Study Section (MCHA)
Project Start
1985-09-30
Project End
2000-03-31
Budget Start
1996-06-20
Budget End
1997-03-31
Support Year
9
Fiscal Year
1996
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Joullié, Madeleine M; Berritt, Simon; Hamel, Ernest (2011) Structure-activity relationships of ustiloxin analogues. Tetrahedron Lett 52:2136-2139
Lee, Jisun; Berritt, Simon; Prier, Christopher K et al. (2011) Facile ring-opening of azabicyclic [3.1.0]- and [4.1.0]aminocyclopropanes to afford 3-piperidinone and 3-azepinone. Org Lett 13:1083-5
Lassen, Kenneth M; Joullié, Madeleine M (2010) Total synthesis of Lys(3) tamandarin M: a potential affinity ligand. Org Lett 12:5306-9
Lassen, Kenneth M; Lee, Jisun; Joullié, Madeleine M (2010) An efficient synthesis of the tamandarin B macrocycle. Tetrahedron Lett 51:1635-1638
Lassen, Kenneth M; Lee, Jisun; Joullie, Madeleine M (2010) Synthetic studies of tamandarin B side chain analogues. J Org Chem 75:3027-36
Shangguan, Ning; Joullié, Madeleine (2009) Total Synthesis of Isoroquefortine E and Phenylahistin. Tetrahedron Lett 50:6755-6757
Shangguan, Ning; Joullié, Madeleine (2009) A Copper-Carbodiimide Approach to the Phomopsin Tripeptide Side Chain. Tetrahedron Lett 50:6748-6750
Li, Pixu; Evans, Cory D; Wu, Yongzhong et al. (2008) Evolution of the total syntheses of ustiloxin natural products and their analogues. J Am Chem Soc 130:2351-64
Forbeck, Erin M; Evans, Cory D; Gilleran, John A et al. (2007) A regio- and stereoselective approach to quaternary centers from chiral trisubstituted aziridines. J Am Chem Soc 129:14463-9
Adrio, Javier; Cuevas, Carmen; Manzanares, Ignacio et al. (2007) Total synthesis and biological evaluation of tamandarin B analogues. J Org Chem 72:5129-38

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