Gregory M. Schaaf

University of North Carolina at Chapel Hill — United States

Chemistry · Physical Sciences

8h-index436citations15works0.02yr avg
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Research Topics

Synthetic Organic Chemistry Methods(5), Chemical synthesis and alkaloids(4), Marine Sponges and Natural Products(3), Beetle Biology and Toxicology Studies(3), Organic Electronics and Photovoltaics(2)

Publications15 total

Total Synthesis of Irciniastatin A (Psymberin)
UNC Libraries·2020Open Access
Substituted N-{3-[(1,1-dioxido-1,2-benzothiazol-3-yl)(phenyl)amino]propyl}benzamide analogs as potent Kv1.3 ion channel blockers. Part 2
Bioorganic & Medicinal Chemistry Letters·2010· 12 citedOpen Access
ChemInform Abstract: Total Synthesis of Irciniastatin A (Psymberin).
ChemInform·2010
Total Synthesis of Irciniastatin A (Psymberin)
Organic Letters·2009· 46 citedOpen Access
ChemInform Abstract: Conjugate Addition of Sodium Methanesulfinate to Vinyl Pyridines and Diazines for the Synthesis of Aliphatic Sulfones.
ChemInform·2009
Conjugate addition of sodium methanesulfinate to vinyl pyridines and diazines for the synthesis of aliphatic sulfones
Tetrahedron Letters·2009· 16 cited
Leptostatin: A synthetic hybrid of the cytotoxic polyketides callystatin A and leptomycin B
Bioorganic & Medicinal Chemistry Letters·2005· 14 cited
Synthesis of the C6−C21 Segment of Amphidinolide E
Organic Letters·2005· 41 cited
Total Synthesis and Structure Confirmation of Leptofuranin D (I).
ChemInform·2004
Total Synthesis and Structure Confirmation of Leptofuranin D
The Journal of Organic Chemistry·2003· 61 cited
ChemInform Abstract: Synthesis of Stereopentad Analogues of the C14—C22 Segment of Callystatin A Through Additions of Chiral Allenylzinc Reagents to Stereotriads.
ChemInform·2002
Synthesis of Stereopentad Analogues of the C14−C22 Segment of Callystatin A through Additions of Chiral Allenylzinc Reagents to Stereotriads
The Journal of Organic Chemistry·2001· 59 cited
Reviews
American Indian Culture and Research Journal·2000
ChemInform Abstract: A New Family of Highly Emissive Soluble Poly(p‐phenylene vinylene) Derivatives. A Step Toward Fully Conjugated Blue‐Emitting Poly(p‐phenylene vinylenes).
ChemInform·1998
A New Family of Highly Emissive Soluble Poly(<i>p</i>-phenylene vinylene) Derivatives. A Step toward Fully Conjugated Blue-Emitting Poly(<i>p</i>-phenylene vinylenes)
Journal of the American Chemical Society·1998· 187 cited

Frequent Co-authors

James A. Marshall(6), Michael T. Crimmins(3), Jason M. Stevens(3), Eric Forsythe(2), William A. Feld(2), Sabuj Mukherjee(2), Alex G. Waterson(2), Bing R. Hsieh(1), Yuan Yu(1), Andrew Nolting(1), Ann M. Mikowski(1), Matthew P. Bourbeau(1), Frederick A. Valeriote(1), Curt D. Haffner(1), Stephen A. Thomson(1), Yu Guo(1), Kimberly G. Petrov(1), Andrew L. Larkin(1), Pierette Banker(1), Scott H. Dickerson(1)