Jason A. Smulik, Ph.D. - Publications
Affiliations: | 2002 | State University of New York, Buffalo, Buffalo, NY, United States |
Area:
Organic ChemistryYear | Citation | Score | |||
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2010 | Smulik JA, Giessert AJ, Diver ST. ChemInform Abstract: Ethylene Metathesis of Sulfur-Containing Alkynes. Cheminform. 33: no-no. DOI: 10.1002/chin.200214068 | 0.725 | |||
2003 | Smulik JA, Vedejs E. Improved reagent for electrophilic amination of stabilized carbanions. Organic Letters. 5: 4187-90. PMID 14572281 DOI: 10.1021/Ol035629W | 0.602 | |||
2002 | Smulik JA, Diver ST, Pan F, Liu JO. Synthesis of cyclosporin A-derived affinity reagents by olefin metathesis. Organic Letters. 4: 2051-4. PMID 12049515 DOI: 10.1021/Ol0258987 | 0.678 | |||
2002 | Smulik JA, Giessert AJ, Diver ST. Ethylene metathesis of sulfur-containing alkynes Tetrahedron Letters. 43: 209-211. DOI: 10.1016/S0040-4039(01)02098-6 | 0.715 | |||
2002 | Smulik JA, Giessert AJ, Diver ST. Ethylene metathesis of sulfur-containing alkynes Tetrahedron Letters. 43: 209-211. | 0.766 | |||
2001 | Rivas FM, Riaz U, Giessert A, Smulik JA, Diver ST. A versatile synthesis of substituted benzimidazolium salts by an amination/ring closure sequence. Organic Letters. 3: 2673-6. PMID 11506606 DOI: 10.1021/Ol016254M | 0.679 | |||
2001 | Smulik JA, Diver ST. Tandem dienyne cross-metathesis/ring-closing metathesis Tetrahedron Letters. 42: 171-174. DOI: 10.1016/S0040-4039(00)01922-5 | 0.755 | |||
2001 | Smulik JA, Diver ST. ChemInform Abstract: Tandem Dienyne Cross-Metathesis/Ring-Closing Metathesis. Cheminform. 32: no-no. DOI: 10.1002/chin.200116078 | 0.68 | |||
2000 | Smulik JA, Diver ST. Expanded scope in ethylene-alkyne cross-metathesis: coordinating heteroatom functionality at the propargylic position. Organic Letters. 2: 2271-4. PMID 10930261 DOI: 10.1021/Ol006035L | 0.707 | |||
2000 | Smulik JA, Diver ST. Terminal Alkyne-Ethylene Cross-Metathesis: Reaction of 1-Substituted Propargyl Esters at Elevated Ethylene Pressure. The Journal of Organic Chemistry. 65: 1788-1792. PMID 10814152 DOI: 10.1021/Jo9916941 | 0.7 | |||
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