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Matthew D. Surman, Ph.D.

Affiliations: 
2002 University of Notre Dame, Notre Dame, IN, United States 
Area:
chemical and enzymatic synthesis and study of biologically important, heteroatom-containing systems including amino acids, peptides, antibiotics, siderophores, and others
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"Matthew Surman"
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Marvin J. Miller grad student 2002 Notre Dame
 (Functionally diverse molecular scaffolds from the regio- and stereoselective metal -mediated ring openings of acylnitroso-derived cycloadducts.)

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Publications

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Surman MD, Mulvihill MJ, Miller MJ. (2010) ChemInform Abstract: Novel 1,4-Benzodiazepines from Acylnitroso-Derived Hetero-Diels-Alder Cycloadducts. Cheminform. 33: no-no
Surman MD, Mulvihill MJ, Miller MJ. (2010) ChemInform Abstract: Novel α-Substituted β-Amino Diesters from Acylnitroso-Derived Hetero-Diels-Alder Cycloadducts. Cheminform. 33: no-no
MULVIHILL MJ, SURMAN MD, MILLER MJ. (2010) ChemInform Abstract: Regio- and Stereoselective Fe(III)- and Pd(0)-Mediated Ring Openings of 3-Aza-2-oxabicyclo[2.2.1]hept-5-ene Systems. Cheminform. 29: no-no
Lee W, Kim KH, Surman MD, et al. (2003) Stereo- and regioselectivity of Pd(0)/InI-mediated allylic additions to aldehydes and ketones. In situ generation of allylindium(III) intermediates from N-acylnitroso Diels-Alder cycloadducts and 1-amino-4-acetoxycyclopentenes. The Journal of Organic Chemistry. 68: 139-49
Surman MD, Mulvihill MJ, Miller MJ. (2002) Regio- and stereoselective ring openings of 3-Aza-2-oxabicyclo[2.2.1]hept-5-ene systems with copper catalyst-modified grignard reagents: application to the synthesis of an inhibitor of 5-lipoxygenase. The Journal of Organic Chemistry. 67: 4115-21
Surman MD, Mulvihill MJ, Miller MJ. (2002) Novel 1,4-benzodiazepines from acylnitroso-derived hetero-Diels-Alder cycloadducts. Organic Letters. 4: 139-41
Surman MD, Mulvihill MJ, Miller MJ. (2002) Novel α-substituted β-amino diesters from acylnitroso-derived hetero-Diels-Alder cycloadducts Tetrahedron Letters. 43: 1131-1134
Surman MD, Miller MJ. (2001) Regio- and stereochemically controlled formation of hydroxamic acid containing anti- or syn-1,4-cycloalkenols from acylnitroso-derived Diels-Alder adducts. The Journal of Organic Chemistry. 66: 2466-9
Surman MD, Miller MJ. (2001) Synthesis of a conformationally restricted substrate analogue of siderophore biosynthetases. Organic Letters. 3: 519-21
Mulvihill MJ, Surman MD, Miller MJ. (1998) Regio- and Stereoselective Fe(III)- and Pd(0)-Mediated Ring Openings of 3-Aza-2-oxabicyclo[2.2.1]hept-5-ene Systems The Journal of Organic Chemistry. 63: 4874-4875
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