Year |
Citation |
Score |
2016 |
Madhusudhan Reddy G, Ko CT, Hsieh KH, Lee CJ, Das U, Lin W. Expanding the scope of primary amine catalysis: Stereoselective synthesis of indanedione-fused 2,6-disubstituted trans-spirocyclohexanones. The Journal of Organic Chemistry. PMID 26907160 DOI: 10.1021/Acs.Joc.5B02921 |
0.432 |
|
2012 |
Deng J, Hsung RP, Ko C. Gassman's cationic [2 + 2] cycloadditions using temporary tethers. Organic Letters. 14: 5562-5. PMID 23098295 DOI: 10.1021/Ol3026796 |
0.633 |
|
2012 |
Tang Y, Yang JH, Liu J, Wang CC, Lv MC, Wu YB, Yu XL, Ko C, Hsung RP. Assembly of the southern macrocyclic half of (+)-spirastrellolide a through cyclic acetal tethered ring-closing metathesis and 1,3-anti-mukaiyama-aldol Heterocycles. 86: 565-598. DOI: 10.3987/Com-12-S(N)54 |
0.661 |
|
2012 |
Feltenberger JB, Ko C, Deng J, Ghosh SK, Hsung RP. Development of an intramolecular gassman's [2 + 2] cycloaddition Heterocycles. 84: 843-878. DOI: 10.3987/Com-11-S(P)65 |
0.732 |
|
2008 |
Ko C, Feltenberger JB, Ghosh SK, Hsung RP. Gassman's intramolecular [2 + 2] cationic cycloaddition. formal total syntheses of raikovenal and epi-raikovenal. Organic Letters. 10: 1971-4. PMID 18422320 DOI: 10.1021/Ol8004968 |
0.742 |
|
2007 |
Ko C, Hsung RP, Al-Rashid ZF, Feltenberger JB, Lu T, Yang JH, Wei Y, Zificsak CA. A stereoselective intramolecular halo-etherification of chiral enamides in the synthesis of halogenated cyclic ethers. Organic Letters. 9: 4459-62. PMID 17910461 DOI: 10.1021/Ol701768N |
0.602 |
|
2007 |
Song Z, Lu T, Hsung RP, Al-Rashid ZF, Ko C, Tang Y. StereoselectiveSimmons-Smith cyclopropanation of chiral enamides. Angewandte Chemie (International Ed. in English). 46: 4069-72. PMID 17458852 DOI: 10.1002/Anie.200700681 |
0.74 |
|
2007 |
Ko C, Hsung RP. An unusual stereoselectivity in the anomeric substitution with carbamates promoted by HNTf2. Organic & Biomolecular Chemistry. 5: 431-4. PMID 17252121 DOI: 10.1039/B615725D |
0.595 |
|
2007 |
Ghosh SK, Ko C, Liu J, Wang J, Hsung RP. A Ketal-Tethered RCM Strategy Toward the Synthesis of Spiroketal Related Natural Products. Cheminform. 38. DOI: 10.1002/chin.200705133 |
0.659 |
|
2006 |
Liu J, Yang JH, Ko C, Hsung RP. Synthesis of the C1-C16 fragment of spirastrellolide A Tetrahedron Letters. 47: 6121-6123. DOI: 10.1016/J.Tetlet.2006.06.067 |
0.689 |
|
2006 |
Ghosh SK, Ko C, Liu J, Wang J, Hsung RP. A ketal-tethered RCM strategy toward the synthesis of spiroketal related natural products Tetrahedron. 62: 10485-10496. DOI: 10.1016/J.Tet.2006.06.113 |
0.734 |
|
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