Maurice A. Marsini

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2003-2008  
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"Maurice Marsini"
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Parents

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Thomas R.R. Pettus grad student 2003-2009 UC Santa Barbara
 (Synthesis and application of aromatic compounds to the total syntheses of mitorubrinic acid and berkelic acid.)
Erik J. Sorensen post-doc Princeton
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Publications

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Marsini MA, Buono FG, Lorenz JC, et al. (2017) Development of a concise, scalable synthesis of a CCR1 antagonist utilizing a continuous flow Curtius rearrangement Green Chemistry. 19: 1454-1461
Wei X, Qu B, Zeng X, et al. (2016) Sequential C-H Arylation and Enantioselective Hydrogenation Enables Ideal Asymmetric Entry to the Indenopiperidine Core of an 11β-HSD-1 Inhibitor. Journal of the American Chemical Society
Liu J, Marsini MA, Bedell TA, et al. (2016) Diastereoselective syntheses of substituted cis-hydrindanones featuring sequential inter- and intramolecular Michael reactions. Tetrahedron. 72: 3713-3717
Visco MD, Reeves JT, Marsini MA, et al. (2016) Triisopropyl borate mediated N-sulfinyl imine formation Tetrahedron Letters
Liu J, Marsini MA, Bedell TA, et al. (2016) Diastereoselective syntheses of substituted cis-hydrindanones featuring sequential inter- and intramolecular Michael reactions Tetrahedron
Marsini MA, Reeves JT, Desrosiers JN, et al. (2015) Diastereoselective Synthesis of α-Quaternary Aziridine-2-carboxylates via Aza-Corey-Chaykovsky Aziridination of N-tert-Butanesulfinyl Ketimino Esters. Organic Letters
Reeves JT, Malapit CA, Buono FG, et al. (2015) Transnitrilation from Dimethylmalononitrile to Aryl Grignard and Lithium Reagents: A Practical Method for Aryl Nitrile Synthesis. Journal of the American Chemical Society. 137: 9481-8
Reeves JT, Visco MD, Marsini MA, et al. (2015) A General Method for Imine Formation Using B(OCH2CF3)3. Organic Letters. 17: 2442-5
Han ZS, Zhang L, Xu Y, et al. (2015) Efficient asymmetric synthesis of structurally diverse P-stereogenic phosphinamides for catalyst design. Angewandte Chemie (International Ed. in English). 54: 5474-7
Reeves JT, Tan Z, Herbage MA, et al. (2013) Carbamoyl anion addition to N-sulfinyl imines: highly diastereoselective synthesis of α-amino amides. Journal of the American Chemical Society. 135: 5565-8
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