San N. Khong, Ph.D.
Affiliations: | 2013 | Chemistry | University of California, Los Angeles, Los Angeles, CA |
Area:
Synthetic Methods, Target-Oriented Synthesis, Chemical DiversityGoogle:
"San Khong"Mean distance: 8.22 | S | N | B | C | P |
Parents
Sign in to add mentor| Ohyun Kwon | grad student | 2013 | UCLA | |
| (Studies Concerning Nucleophilic Phosphine Catalysis and Designs of new Chiral Aminophosphines toward Asymmetric Phosphine-Catalyzed Reactions.) | ||||
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Khong S, Venkatesh T, Kwon O. (2021) Nucleophilic Phosphine Catalysis: The Untold Story. Asian Journal of Organic Chemistry. 10: 2699-2708 |
| Khong SN, Xie C, Wang X, et al. (2019) Chiral aminophosphines derived from hydroxyproline and their application in allene-imine [4 + 2] annulation. The Journal of Antibiotics |
| Xie LX, Williams KJ, He CH, et al. (2015) Resveratrol and para-coumarate serve as ring precursors for coenzyme Q biosynthesis. Journal of Lipid Research. 56: 909-19 |
| Khong S, Kwon O. (2014) Phosphine-Initiated General-Base-Catalyzed Quinolone Synthesis. Asian Journal of Organic Chemistry / Managing Editor, Richard Threlfall. 3: 453-457 |
| Khong S, Kwon O. (2014) ChemInform Abstract: Phosphine-Initiated General-Base-Catalyzed Quinolone Synthesis. Cheminform. 45: no-no |
| Khong S, Kwon O. (2013) ChemInform Abstract: One-Pot Phosphine-Catalyzed Syntheses of Quinolines. Cheminform. 44: no-no |
| Khong S, Kwon O. (2012) One-pot phosphine-catalyzed syntheses of quinolines. The Journal of Organic Chemistry. 77: 8257-67 |
| Khong SN, Kwon O. (2012) Chiral aminophosphines as catalysts for enantioselective double-Michael indoline syntheses. Molecules (Basel, Switzerland). 17: 5626-50 |
| Khong SN, Tran YS, Kwon O. (2010) Equilibrium between a vinylogous ylide and a phosphonium dienolate zwitterion: vinylogous Wittig olefination versus vinylogous aldol-type reaction. Tetrahedron. 66: 4760-4768 |