Dustin J. Mergott - Publications
Affiliations: | 2004 | University of Michigan, Ann Arbor, Ann Arbor, MI |
Year | Citation | Score | |||
---|---|---|---|---|---|
2010 | Frank SA, Mergott DJ, Roush WR. ChemInform Abstract: The Vinylogous Intramolecular Morita-Baylis-Hillman Reaction: Synthesis of Functionalized Cyclopentenes and Cyclohexenes with Trialkylphosphines as Nucleophilic Catalysts. Cheminform. 33: no-no. DOI: 10.1002/chin.200232041 | 0.662 | |||
2008 | Mergott DJ, Zuend SJ, Jacobsen EN. Catalytic asymmetric total synthesis of (+)-yohimbine. Organic Letters. 10: 745-8. PMID 18257582 DOI: 10.1021/Ol702781Q | 0.723 | |||
2008 | Winbush SM, Mergott DJ, Roush WR. Total synthesis of (-)-spinosyn A: examination of structural features that govern the stereoselectivity of the key transannular Diels-Alder reaction. The Journal of Organic Chemistry. 73: 1818-29. PMID 18215065 DOI: 10.1021/Jo7024515 | 0.566 | |||
2008 | Mergott DJ. ChemInform Abstract: Corey-Winter Olefin Synthesis Cheminform. 39. DOI: 10.1002/chin.200836262 | 0.504 | |||
2008 | Winbush SM, Mergott DJ, Roush WR. ChemInform Abstract: Total Synthesis of (-)-Spinosyn A (Ib): Examination of Structural Features that Govern the Stereoselectivity of the Key Transannular Diels-Alder Reaction. Cheminform. 39. DOI: 10.1002/chin.200829202 | 0.691 | |||
2004 | Mergott DJ, Frank SA, Roush WR. Total synthesis of (-)-spinosyn A. Proceedings of the National Academy of Sciences of the United States of America. 101: 11955-9. PMID 15173590 DOI: 10.1073/Pnas.0401247101 | 0.664 | |||
2002 | Mergott DJ, Frank SA, Roush WR. Application of the intramolecular vinylogous Morita-Baylis-Hillman reaction toward the synthesis of the spinosyn A tricyclic nucleus. Organic Letters. 4: 3157-60. PMID 12201741 DOI: 10.1021/Ol026540D | 0.678 | |||
2002 | Frank SA, Mergott DJ, Roush WR. The vinylogous intramolecular Morita-Baylis-Hillman reaction: synthesis of functionalized cyclopentenes and cyclohexenes with trialkylphosphines as nucleophilic catalysts. Journal of the American Chemical Society. 124: 2404-5. PMID 11890766 DOI: 10.1021/Ja017123J | 0.666 | |||
Show low-probability matches. |