个人简介
National Institutes of Health Postdoctoral Fellowship, 1979-1981
Lilly Distinguished Teaching Fellowship, Chancellor's Citation, American
Cyanamid Academic Award, Teacher-Scholar of the Year (1998)
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Kallmerten, J. and Wittman, M. D., "Recent Applications of Sigmatropic Reactions to the Stereocontrolled Synthesis of Highly-Oxygenated Natural Products" in Studies in Natural Products Chemistry, Vol. 3, Part B: Stereoselective Synthesis, A.ur-Rahman, ed., Elsevier (Amsterdam), 1989, pp. 233-286.
Kallmerten J., Coutts, S. J. and Wittman, M. D., "Synthesis of Antitumor Ansamycins. 1. Serial Sigmatropic Construction of the C11-C21 Ansa System of Macbecin I", Tetrahedron Letters. 31, 4301 (1990).
Coutts, S. J. and Kallmerten J., "Synthesis of Antitumor Ansamycins. 2. A Formal Total Synthesis of Macbecin I", Tetrahedron Letters. 31, 4305 (1990).
Thompson, R. C. and Kallmerten J., "An Annulative, Carbohydrate-Based Approach To Pancratistatin and Structurally Related Phenanthridone Alkaloids. Synthesis of (+)-Tetrabenzyl Lycoricidine", J. Org. Chem. 55, 6076 (1990).
Cywin, C. L., Webster, F. X. and Kallmerten, J., "Synthesis of (-)-(6R,10R)-Matsuone. Assignment of Relative Stereochemistry to a Pheromone of Matsucoccus Pine Bast Scales.", J. Org. Chem. 56, 2953 (1991).
Ostrander, R., Rossano, L. T. and Kallmerten J., "Crystalline Molecular Structure of an Oxa-Bridged Nargenicin Intermediate", Acta Cryst., 2410 (1991).
Cywin, C. L. and Kallmerten, J.,"Enantioselective Synthesis of a Sex Attractant Pheromone of Matsucoccus Feytaudi. The Relative Stereochemistry of the Natural Pheromone is Priority Reflective", J. Natural Prods. 52, 1664 (1991).
Tong, X. and Kallmerten J., "A Stereocontrolled Sigmatropic Route to Tetrasubstituted Acyclic Olefins", Synlett, 845 (1992).
Evans, J., and Kallmerten, J., "A Stereocontrolled Synthetic Approach to the Oxa-Bridged Octalin Nucleus of Coloradocin (Luminamicin)" Synlett, 269 (1992).
N. Sin and J. Kallmerten, "Diastereoselective [2,3] Wittig Rearrangement of Carbohydrate-Derived Tertiary Allylic Ethers. 1. Synthesis of an Advanced Rapamycin Intermediate From D-Glucose", Tetrahedron Letters, 34, 753 (1993).
J. E. Eshelman and J. Kallmerten, "Diastereoselective [2,3] Wittig Rearrangement of Carbohydrate-Derived Tertiary Allylic Ethers. 1. Synthesis of the C11-C18 Subunit of Herbimycin A From D-Glucose", Tetrahedron Letters, 34, 749 (1993).
Durham, L. L., Cywin, C. L. and Kallmerten, J., "Synthesis of Polypropionate-Derived Acyclic Systems. Stereocontrolled Hydroboration of Highly-Functionalized Trisubstituted Acyclic Olefins", Synlett. 696 (1993).
Cywin, C.L. and Kallmerten J., "Iterative Sigmatropic Construction of the C1-C11 Subunit of the Ionophore Antibiotic Zincophorin", Tetrahedron Letters 34, 1131 (1993).
Kallmerten, J., "[2,3] Sigmatropic Reactions", in Houben-Weyl Methods of Organic Chemistry: Stereoselective Synthesis, Vol. E 21, R.W. Hoffman , ed., Thieme (Stuttgart) 3757 (1995).
Kallmerten, J., "[1,2] Sigmatropic Reactions", in Houben-Weyl Methods of Organic Chemistry: Stereoselective Synthesis, Vol. E 21, R.W. Hoffman , ed., Thieme (Stuttgart) 3810.
Shi, X., Webster, F. X., Kallmerten, J. and Meinwald, J., " Diastereoselective [2,3] Wittig Rearrangement of a Tertiary Bisallylic Ether", Tetrahedron Letts. 36, 7197 (1995).
Kallmerten, J., "Chemistry of the Nargenicin Macrolides" in Studies in Natural Products Chemistry, Vol. 17,, A.ur-Rahman, ed., Elsevier (Amsterdam), pp. 283-310
N. Sin and J. Kallmerten, "Synthesis of (2S,3S,8S,9S)-Adda From D-Glucose", Tetrahedron Letters, 37 5645 (1996)
D. M. P. Gigante, F. Long, L. A. Bodack, J. M. Evans, J. Kallmerten, L. A. Nafie and T. B. Freedman, "Hydrogen Stretching Vibrational Circular Dichroism in Methyl Lactate and Related Molecules", J. Phys. Chem. A, 103, 1523, 1999.
Michael P. Hayes, Brian A. Sherer, Xiaohong Tong, Paul J. Hatala, Nilo Zanatta, Philip N. Borer, and James Kallmerten, “Regioselective synthesis of 13C1-labeled 2-deoxyribonolactones”, Tetrahedron, 57 1515 (2001)
Hatala, P.J., Borer, P. N. and Kallmerten, J., "Regioselective Synthesis of 1,3,5-13C3 and 2,4-13C2 Labeled Deoxyribonolactones”, Nucleotides, Nucleosides and Nucleic Acids, 57, 1961 (2001).