| Year |
Citation |
Score |
| 2016 |
Han G, Zhang G, You L, Wang Y, Yang L, Yang J, Zhou L, Yuan M, Zou X, Cheng H. Deflated rims along the Xiangshui River on the Xiliaohe Plain, Northeast China: A case of active fluvial-aeolian interactions Geomorphology. 257: 47-56. DOI: 10.1016/j.geomorph.2015.12.025 |
0.412 |
|
| 2015 |
Wang Q, Cao R, Ning X, You L, Mu C, Wang C, Wei L, Cong M, Wu H, Zhao J. Effects of ocean acidification on immune responses of the Pacific oyster Crassostrea gigas. Fish & Shellfish Immunology. PMID 26706224 DOI: 10.1016/j.fsi.2015.12.025 |
0.347 |
|
| 2015 |
You L, Liang XT, Xu L, Wang YF, Zhang JJ, Su Q, Li Y, Zhang B, Yang SL, Chen JH, Yang Z. Asymmetric Total Synthesis of Propindilactone G. Journal of the American Chemical Society. PMID 26181605 DOI: 10.1021/Jacs.5B06480 |
0.306 |
|
| 2015 |
You L, Yuan F, Ma F. Synthesis of mesoporous NH2-SBA-15 by a simple and efficient strategy Russian Journal of Physical Chemistry A. 89: 2298-2303. DOI: 10.1134/S0036024415120183 |
0.315 |
|
| 2011 |
Buchanan GS, Cole KP, Li G, Tang Y, You LF, Hsung RP. Constructing the Architecturally Distinctive ABD-Tricycle of Phomactin A through an Intramolecular Oxa-[3 + 3] Annulation Strategy. Tetrahedron. 67: 10105-10118. PMID 23750054 DOI: 10.1016/J.Tet.2011.09.111 |
0.731 |
|
| 2008 |
You LF, Hsung RP, Bedermann AA, Kurdyumov AV, Tang Y, Buchanan GS, Cole KP. An Enantioselective Synthesis of the ABD Tricycle for (-)-Phomactin A Featuring Rawal's Asymmetric Diels-Alder Cycloaddition. Advanced Synthesis & Catalysis. 350. PMID 24273477 DOI: 10.1002/Adsc.200800552 |
0.724 |
|
| 2008 |
You LF, Hsung RP, Bedermann AA, Kurdyumov AV, Tang Y, Buchanan GS, Cole KP. An Enantioselective Synthesis of the ABD Tricycle for (-)-Phomactin A Featuring Rawal's Asymmetric Diels-Alder Cycloaddition. Advanced Synthesis & Catalysis. 350: 2885-2891. PMID 20351791 |
0.733 |
|
| 2007 |
Li H, You L, Zhang X, Johnson WL, Figueroa R, Hsung RP. Syntheses of amide-substituted isoxazoles and pyrazoles via regioselective [3 + 2] cycloadditions of terminally unsubstituted ynamides Heterocycles. 74: 553-568. DOI: 10.3987/Com-07-S(W)34 |
0.662 |
|
| 2007 |
You L, Al-Rashid ZF, Figueroa R, Ghosh SK, Li G, Lu T, Hsung RP. A two-carbon homologation of aldehydes and ketones using ynamides Synlett. 1656-1662. DOI: 10.1055/S-2007-984513 |
0.667 |
|
| 2006 |
Zhang X, Hsung RP, You L. Tandem azidination- and hydroazidination-Huisgen [3 + 2] cycloadditions of ynamides. Synthesis of chiral amide-substituted triazoles. Organic & Biomolecular Chemistry. 4: 2679-82. PMID 16826290 DOI: 10.1039/B606680A |
0.699 |
|
| 2006 |
Tang Y, Oppenheimer J, Song Z, You L, Zhang X, Hsung RP. Strategies and approaches for constructing 1-oxadecalins Tetrahedron. 62: 10785-10813. DOI: 10.1016/J.Tet.2006.08.054 |
0.63 |
|
| 2006 |
Zhang X, Li H, You L, Tang Y, Hsung RP. Copper salt-catalyzed azide-[3 + 2] cycloadditions of ynamides and bis-ynamides Advanced Synthesis and Catalysis. 348: 2437-2442. DOI: 10.1002/Adsc.200600404 |
0.694 |
|
| 2005 |
Brummond KM, You L. Consecutive Rh(I)-catalyzed Alder-ene/Diels-Alder/Diels-Alder reaction sequence affording rapid entry to polycyclic compounds Tetrahedron. 61: 6180-6185. DOI: 10.1016/j.tet.2005.03.141 |
0.303 |
|
| 2002 |
Brummond KM, Chen H, Sill P, You L. A rhodium(I)-catalyzed formal allenic Alder ene reaction for the rapid and stereoselective assembly of cross-conjugated trienes. Journal of the American Chemical Society. 124: 15186-7. PMID 12487589 DOI: 10.1021/Ja027588P |
0.311 |
|
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