Bonan Cao, Ph.D. - Publications

Affiliations: 
2013 Chemistry and Chemical Biology Rutgers University, New Brunswick, New Brunswick, NJ, United States 
Area:
Synthetic organic, inorganic and organometallic chemistry

13 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2015 Allegretti JR, Borges L, Lucci M, Chang M, Cao B, Collins E, Vogel B, Arthur E, Emmons D, Korzenik JR. Risk Factors for Rehospitalization Within 90 Days in Patients with Inflammatory Bowel Disease. Inflammatory Bowel Diseases. 21: 2583-9. PMID 26244647 DOI: 10.1097/MIB.0000000000000537  0.404
2014 Zheng X, Cao B, Zhang X. Synthesis of 4-aryl-2,3-dihydropyrroles via Rh-catalyzed intramolecular hydroamino-methylation reaction Tetrahedron Letters. 55: 4489-4491. DOI: 10.1016/J.Tetlet.2014.06.011  0.524
2013 Zhang X, Xu L, Shen J, Cao B, Cheng T, Zhao T, Liu X, Zhang H. Metabolic signatures of esophageal cancer: NMR-based metabolomics and UHPLC-based focused metabolomics of blood serum. Biochimica Et Biophysica Acta. 1832: 1207-16. PMID 23524237 DOI: 10.1016/j.bbadis.2013.03.009  0.312
2013 Zhang X, Shen J, Cao B, Xu L, Zhao T, Liu X, Zhang H. Metabolomic investigation of Arthus reaction in a rat model using proton nuclear magnetic resonance (1H NMR) spectroscopy and rapid resolution liquid chromatography (RRLC). Molecular Biosystems. 9: 1423-35. PMID 23511749 DOI: 10.1039/c3mb25412g  0.312
2013 Zheng X, Cao B, Liu T, Zhang X. Rhodium‐Catalyzed Asymmetric Hydroformylation of 1,1‐Disubstituted Allylphthalimides: A Catalytic Route to β3‐Amino Acids Advanced Synthesis & Catalysis. 355: 679-684. DOI: 10.1002/Adsc.201200960  0.508
2012 Li S, Huang K, Cao B, Zhang J, Wu W, Zhang X. Highly enantioselective hydrogenation of β,β-disubstituted nitroalkenes. Angewandte Chemie (International Ed. in English). 51: 8573-6. PMID 22807193 DOI: 10.1002/Anie.201202715  0.577
2012 Cai C, Yu S, Cao B, Zhang X. New tetraphosphorus ligands for highly linear selective hydroformylation of allyl and vinyl derivatives. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 9992-8. PMID 22782739 DOI: 10.1002/Chem.201201396  0.684
2012 Liu G, Huang K, Cao B, Chang M, Li S, Yu S, Zhou L, Wu W, Zhang X. Highly regioselective isomerization-hydroaminomethylation of internal olefins catalyzed by Rh complex with Tetrabi-type phosphorus ligands. Organic Letters. 14: 102-5. PMID 22149490 DOI: 10.1021/Ol202848A  0.71
2011 Liu G, Huang K, Cai C, Cao B, Chang M, Wu W, Zhang X. Highly regioselective hydroaminomethylation of terminal olefins to linear amines using Rh complexes with a Tetrabi phosphorus ligand. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 14559-63. PMID 22105788 DOI: 10.1002/Chem.201103073  0.689
2010 Huang K, Zhang X, Emge TJ, Hou G, Cao B, Zhang X. Design and synthesis of a novel three-hindered quadrant bisphosphine ligand and its application in asymmetric hydrogenation. Chemical Communications (Cambridge, England). 46: 8555-7. PMID 20944852 DOI: 10.1039/C0Cc02620D  0.688
2010 Zhang X, Huang K, Hou G, Cao B, Zhang X. Electron-donating and rigid P-stereogenic bisphospholane ligands for highly enantioselective rhodium-catalyzed asymmetric hydrogenations. Angewandte Chemie (International Ed. in English). 49: 6421-4. PMID 20661983 DOI: 10.1002/Anie.201002990  0.664
2010 Zhang X, Cao B, Yu S, Zhang X. Rhodium-catalyzed asymmetric hydroformylation of N-allylamides: highly enantioselective approach to beta2-amino aldehydes. Angewandte Chemie (International Ed. in English). 49: 4047-50. PMID 20506436 DOI: 10.1002/Anie.201000955  0.548
2010 Zhang X, Cao B, Yan Y, Yu S, Ji B, Zhang X. Synthesis and application of modular phosphine-phosphoramidite ligands in asymmetric hydroformylation: structure-selectivity relationship. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 871-7. PMID 19950337 DOI: 10.1002/Chem.200902238  0.712
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