Jennifer Lafontaine
Affiliations: | 1993-1998 | Chemistry | University of California, Berkeley, Berkeley, CA, United States |
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| Lafontaine JA, Provencal DP, Gardelli C, et al. (2010) ChemInform Abstract: The Enantioselective Total Synthesis of the Antitumor Macrolide Natural Product Rhizoxin D. Cheminform. 30: no-no |
| PROVENCAL DP, GARDELLI C, LAFONTAINE JA, et al. (2010) ChemInform Abstract: Rhizoxin Synthetic Studies. Part 2. Synthesis of the Left Hand (C(10) to C(19)) and Polyene Fragments. Cheminform. 26: no-no |
| LAFONTAINE JA, LEAHY JW. (2010) ChemInform Abstract: Rhizoxin Synthetic Studies. Part 1. Synthesis of the Right Hand (C(1) to C(9)) Portion via a “Pinwheel” Approach. Cheminform. 26: no-no |
| Humphries PS, Lafontaine JA, Agree CS, et al. (2009) Synthesis and SAR of 4-substituted-2-aminopyrimidines as novel c-Jun N-terminal kinase (JNK) inhibitors. Bioorganic & Medicinal Chemistry Letters. 19: 2099-102 |
| Lafontaine JA, Provencal DP, Gardelli C, et al. (2003) Enantioselective total synthesis of the antitumor macrolide rhizoxin D. The Journal of Organic Chemistry. 68: 4215-34 |
| Lafontaine JA, Provencal DP, Gardelli C, et al. (1999) The enantioselective total synthesis of the antitumor macrolide natural product rhizoxin D Tetrahedron Letters. 40: 4145-4148 |
| Provencal DP, Gardelli C, Lafontaine JA, et al. (1995) Rhizoxin synthetic studies. 2. Synthesis of the left hand [C(10) to C(19)] and polyene fragments Tetrahedron Letters. 36: 6033-6036 |
| Lafontaine JA, Leahy JW. (1995) Rhizoxin synthetic studies. 1. Synthesis of the right hand [C(1) to C(9)]portion via a “pinwheel” approach Tetrahedron Letters. 36: 6029-6032 |