Year |
Citation |
Score |
2016 |
Chung WJ, Vanderwal CD. Stereoselective Halogenation in Natural Product Synthesis. Angewandte Chemie (International Ed. in English). PMID 26833878 DOI: 10.1002/Anie.201506388 |
0.518 |
|
2015 |
Shin YS, Lee SW, Park K, Chung WS, Kim SW, Hyun JS, Moon DG, Yang SK, Ryu JK, Yang DY, Moon KH, Min KS, Park JK. Effect of levitra on sustenance of erection (EROS): an open-label, prospective, multicenter, single-arm study to investigate erection duration measured by stopwatch with flexible dose vardenafil administered for 8 weeks in subjects with erectile dysfunction. International Journal of Impotence Research. 27: 95-102. PMID 25471318 DOI: 10.1038/ijir.2014.39 |
0.301 |
|
2014 |
Chung WJ, Carlson JS, Vanderwal CD. General approach to the synthesis of the chlorosulfolipids danicalipin A, mytilipin A, and malhamensilipin A in enantioenriched form. The Journal of Organic Chemistry. 79: 2226-41. PMID 24494597 DOI: 10.1021/Jo5000829 |
0.578 |
|
2014 |
Chung WJ, Vanderwal CD. Approaches to the chemical synthesis of the chlorosulfolipids. Accounts of Chemical Research. 47: 718-28. PMID 24400674 DOI: 10.1021/Ar400246W |
0.579 |
|
2014 |
Chung W, Carlson JS, Vanderwal CD. ChemInform Abstract: General Approach to the Synthesis of the Chlorosulfolipids Danicalipin A (I), Mytilipin A (II), and Malhamensilipin A (III) in Enantioenriched Form. Cheminform. 45: no-no. DOI: 10.1002/chin.201434213 |
0.511 |
|
2013 |
Chung WJ, Carlson JS, Bedke DK, Vanderwal CD. A synthesis of the chlorosulfolipid mytilipin A via a longest linear sequence of seven steps. Angewandte Chemie (International Ed. in English). 52: 10052-5. PMID 23929596 DOI: 10.1002/Anie.201304565 |
0.566 |
|
2008 |
Denmark SE, Chung WJ. Lewis base activation of Lewis acids: catalytic, enantioselective addition of glycolate-derived silyl ketene acetals to aldehydes. The Journal of Organic Chemistry. 73: 4582-95. PMID 18505296 DOI: 10.1021/Jo8006539 |
0.334 |
|
2008 |
Denmark SE, Chung WJ. Lewis base activation of Lewis acids: catalytic enantioselective glycolate aldol reactions. Angewandte Chemie (International Ed. in English). 47: 1890-2. PMID 18236504 DOI: 10.1002/Anie.200705499 |
0.332 |
|
2006 |
Denmark SE, Chung WJ. Lewis base catalyzed addition of trimethylsilyl cyanide to aldehydes. The Journal of Organic Chemistry. 71: 4002-5. PMID 16674085 DOI: 10.1021/Jo060153Q |
0.359 |
|
2002 |
Kim S, Lim CJ, Song C, Chung WJ. Novel radical alkylation of carboxylic imides. Journal of the American Chemical Society. 124: 14306-7. PMID 12452695 DOI: 10.1021/Ja028396X |
0.377 |
|
2001 |
Kim S, Kim N, Chung W, Cho CH. Free Radical Acylation Approaches of C-H Bonds with 2-Chloroethylsulfonyl Oxime Ethers Synlett. 2001: 0937-0940. DOI: 10.1055/S-2001-14627 |
0.357 |
|
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