| Year |
Citation |
Score |
| 2010 |
Lawlor MD, Lee TW, Danheiser RL. ChemInform Abstract: Rhodium-Catalyzed Rearrangement of α-Diazo Thiol Esters to Thio-Substituted Ketenes. Application in the Synthesis of Cyclobutanones, Cyclobutenones, and β-Lactams. Cheminform. 31: no-no. DOI: 10.1002/chin.200046086 |
0.51 |
|
| 2010 |
DANHEISER RL, LEE TW, MENICHINCHERI M, BRUNELLI S, NISHIUCHI M. ChemInform Abstract: Synthesis of Alkylidenecyclopropanes via Thermal Cycloreversion of . alpha.-Spirocyclopropyl-β-lactones. Cheminform. 28: no-no. DOI: 10.1002/chin.199742093 |
0.479 |
|
| 2003 |
Danheiser RL, Okamoto I, Lawlor MD, Lee TW. Generation and [2+2] cycloadditions of thio-substituted ketenes: Trans-1-(4-methoxyphenyl)-4-phenyl-3-(phenylthio)azetidin-2-one (2-azetidinone, 1-(4-methoxyphenyl)-4-phenyl-3-(phenylthio)-, trans-) Organic Syntheses. 80: 160-171. |
0.501 |
|
| 2002 |
Ryu DH, Lee TW, Corey EJ. Broad-spectrum enantioselective diels-alder catalysis by chiral, cationic oxazaborolidines. Journal of the American Chemical Society. 124: 9992-3. PMID 12188655 DOI: 10.1021/Ja027468H |
0.603 |
|
| 2002 |
Corey EJ, Shibata T, Lee TW. Asymmetric Diels-Alder reactions catalyzed by a triflic acid activated chiral oxazaborolidine. Journal of the American Chemical Society. 124: 3808-9. PMID 11942799 DOI: 10.1021/Ja025848X |
0.405 |
|
| 2001 |
Lee TW, Corey EJ. (2-methoxyphenyl)dimethylsilyl lithium and cuprate reagents offer unique advantages in multistep synthesis. Organic Letters. 3: 3337-9. PMID 11594828 DOI: 10.1021/Ol0165746 |
0.32 |
|
| 2001 |
Lee TW, Corey EJ. Enantioselective total synthesis of eunicenone A. Journal of the American Chemical Society. 123: 1872-7. PMID 11456807 DOI: 10.1021/Ja004043R |
0.407 |
|
| 2001 |
Corey EJ, Lee TW. The formyl C-H···O hydrogen bond as a critical factor in enantioselective Lewis-acid catalyzed reactions of aldehydes Chemical Communications. 1321-1329. |
0.396 |
|
| 2000 |
Lawlor MD, Lee TW, Danheiser RL. Rhodium-catalyzed rearrangement of alpha-diazo thiol esters to thio-substituted ketenes. Application in the synthesis of cyclobutanones, cyclobutenones, and beta-lactams. The Journal of Organic Chemistry. 65: 4375-84. PMID 10891141 DOI: 10.1021/jo000227c |
0.513 |
|
| 1997 |
Danheiser RL, Lee TW, Menichincheri M, Brunelli S, Nishiuchi M. Synthesis of alkylidenecyclopropanes via thermal cycloreversion of α-spirocyclopropyl-β-lactones Synlett. 469-470. DOI: 10.1055/S-1997-6134 |
0.468 |
|
| 1997 |
Corey EJ, Barnes-Seeman D, Lee TW, Goodman SN. A transition-state model for the Mikami enantioselective ene reaction Tetrahedron Letters. 38: 6513-6516. DOI: 10.1016/S0040-4039(97)01517-7 |
0.719 |
|
| 1997 |
Corey EJ, Lee TW. Enantioselective Diels-Alder reactions between cyclopentadiene and α,β-acetylenic aldehydes catalyzed by a chiral super Lewis acid Tetrahedron Letters. 38: 5755-5758. DOI: 10.1016/S0040-4039(97)01287-2 |
0.394 |
|
| 1997 |
Corey EJ, Barnes-Seeman D, Lee TW. The formyl C-H--O hydrogen bond as a critical factor in enantioselective reactions of aldehydes, Part 4, aldol, ethylation, hydrocyanation and Diels-Alder reactions catalyzed by chiral Bb, Ti and a1 Lewis acids Tetrahedron Letters. 38: 4351-4354. DOI: 10.1016/S0040-4039(97)00932-5 |
0.732 |
|
| 1997 |
Corey EJ, Barnes-Seeman D, Lee TW. The formyl C-H--O hydrogen bond as a key to transition-state organization in enantioselective allylation, aldol and Diels-Alder reactions catalyzed by chiral Lewis acids Tetrahedron Letters. 38: 1699-1702. DOI: 10.1016/S0040-4039(97)00193-7 |
0.735 |
|
| 1997 |
Corey EJ, Barnes-Seeman D, Lee TW. The mechanistic basis for diastereoselectivity in the Matteson rearrangement Tetrahedron Asymmetry. 8: 3711-3713. |
0.715 |
|
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