Maurice A. Marsini

发表

Sequential C-H Arylation and Enantioselective Hydrogenation Enables Ideal Asymmetric Entry to the Indenopiperidine Core of an 11β-HSD-1 Inhibitor.

Jinhua J. Song, Bing-Shiou Yang, Jun Wang, 2016, Journal of the American Chemical Society.

A General Method for Imine Formation Using B(OCH2CF3)3.

C. Senanayake, N. Grinberg, C. Busacca, 2015, Organic letters.

A Practical Procedure for Reduction of Primary, Secondary and Tertiary Amides to Amines

C. Senanayake, Heewon Lee, B. Lu, 2013 .

Large-Scale Enantioselective Reduction of 2,3-Disubstituted Indenopyridine Enables a Practical Manufacturing Process for an 11β-HSD-1 Inhibitor

Jinhua J. Song, Bing-Shiou Yang, Jun Wang, 2021, Organic Process Research & Development.

Addition of Non-Stabilized Carbon-Based Nucleophilic Reagents to ChiralN-Sulfinyl Imines

C. Senanayake, K. Fandrick, J. Sieber, 2019, Organic Reactions.

Total synthesis of (+/-)-mitorubrinic acid.

T. Pettus, Maurice A. Marsini, K. M. Gowin, 2006, Organic letters.

Transnitrilation from Dimethylmalononitrile to Aryl Grignard and Lithium Reagents: A Practical Method for Aryl Nitrile Synthesis.

C. Senanayake, K. Fandrick, Christian A. Malapit, 2015, Journal of the American Chemical Society.

Tuning the Peri Effect for Enantioselectivity: Asymmetric Hydrogenation of Unfunctionalized Olefins with the BIPI Ligands

Dajun Chen, C. Senanayake, K. Fandrick, 2013 .

Synthesis of resorcinol derived spironitronates.

T. Pettus, Yaodong Huang, Maurice A. Marsini, 2007, Organic letters.

Diastereoselective Synthesis of α-Quaternary Aziridine-2-carboxylates via Aza-Corey-Chaykovsky Aziridination of N-tert-Butanesulfinyl Ketimino Esters.

C. Senanayake, Xudong Wei, K. Fandrick, 2015, Organic letters.

Diastereoselective syntheses of chroman spiroketals via [4 + 2] cycloaddition of enol ethers and o-quinone methides.

Kun-Liang Wu, T. Pettus, Yaodong Huang, 2008, Organic letters.

A General Method for Imine Formation Using B(OCH2CF3)3.

C. Senanayake, N. Grinberg, C. Busacca, 2015, Organic letters.

Carbamoyl anion addition to N-sulfinyl imines: highly diastereoselective synthesis of α-amino amides.

C. Senanayake, K. Fandrick, Shengli Ma, 2013, Journal of the American Chemical Society.

Efficient asymmetric synthesis of structurally diverse P-stereogenic phosphinamides for catalyst design.

Jinhua J. Song, C. Senanayake, N. Yee, 2015, Angewandte Chemie.

Development of a concise, scalable synthesis of a CCR1 antagonist utilizing a continuous flow Curtius rearrangement

Jinhua J. Song, B. Narayanan, Bing-Shiou Yang, 2017 .

Triisopropyl borate mediated N-sulfinyl imine formation

C. Senanayake, C. Busacca, I. Volchkov, 2016 .

Chemoselective reactions of 3-benzyloxy-1,2-o-quinone with organometallic reagents.

T. Pettus, Luke A. Miller, Maurice A. Marsini, 2009, Organic letters.

Diastereoselective syntheses of substituted cis-hydrindanones featuring sequential inter- and intramolecular Michael reactions.

E. J. Sorensen, P. Reider, Junjia Liu, 2016, Tetrahedron.

A concise and convergent synthesis of PA-824.

E. J. Sorensen, P. Reider, Maurice A. Marsini, 2010, The Journal of organic chemistry.

Optimization of an Azaindazole Series of CCR1 Antagonists and Development of a Semicontinuous-Flow Synthesis

F. Buono, Jon C. Lorenz, H. Razavi, 2019, ACS Symposium Series.

Potent and selective CC chemokine receptor 1 antagonists labeled with carbon-13, carbon-14, and tritium.

C. Senanayake, B. Latli, C. Busacca, 2018, Journal of labelled compounds & radiopharmaceuticals.

Diastereoselective syntheses of chroman spiroketals via [4 + 2] cycloaddition of enol ethers and o-quinone methides.

Kun-Liang Wu, T. Pettus, Yaodong Huang, 2008, Organic letters.