| Year |
Citation |
Score |
| 2016 |
Lu K, Ding F, Qin L, Jia X, Xu C, Zhao X, Yao Q, Yu P. Synthesis of Substituted Pyrroles via Copper-catalyzed Cyclization of Ethyl Allenoates with Activated Isocyanides. Chemistry, An Asian Journal. PMID 27348611 DOI: 10.1002/Asia.201600761 |
0.386 |
|
| 2014 |
Wang H, Yan Z, Lei Y, Sheng K, Yao Q, Lu K, Yu P. Concise synthesis of prenylated and geranylated chalcone natural products by regiospecific iodination and Suzuki coupling reactions Tetrahedron Letters. 55: 897-899. DOI: 10.1016/J.Tetlet.2013.12.044 |
0.326 |
|
| 2012 |
Liu TL, Zhang HX, Zheng Y, Yao Q, Ma JA. Catalytic enantioselective addition of terminal 1,3-diynes to N-sulfonyl aldimines: access to chiral diynylated carbinamines. Chemical Communications (Cambridge, England). 48: 12234-6. PMID 23146913 DOI: 10.1039/c2cc37290h |
0.474 |
|
| 2007 |
Yao Q, Zabawa M, Woo J, Zheng C. Carbocyclic carbene ligands derived from aromatic nitrones: formation and catalytic activity of their Pd(II) complexes. Journal of the American Chemical Society. 129: 3088-9. PMID 17311389 DOI: 10.1021/ja0701659 |
0.552 |
|
| 2006 |
Yao Q, Sheets M. A SeCSe-Pd(II) pincer complex as a highly efficient catalyst for allylation of aldehydes with allyltributyltin. The Journal of Organic Chemistry. 71: 5384-7. PMID 16808533 DOI: 10.1021/Jo060456K |
0.623 |
|
| 2004 |
Yao Q, Kinney EP, Zheng C. Selenium-ligated palladium(II) complexes as highly active catalysts for carbon-carbon coupling reactions: the Heck reaction. Organic Letters. 6: 2997-9. PMID 15330667 DOI: 10.1021/Ol0486977 |
0.5 |
|
| 2004 |
Yao Q, Zhang Y. Poly(fluoroalkyl acrylate)-bound ruthenium carbene complex: a fluorous and recyclable catalyst for ring-closing olefin metathesis. Journal of the American Chemical Society. 126: 74-5. PMID 14709066 DOI: 10.1021/ja037394p |
0.64 |
|
| 2004 |
Yao Q, Rodriguez Motta A. Immobilization of the Grubbs second-generation ruthenium-carbene complex on poly(ethylene glycol): a highly reactive and recyclable catalyst for ring-closing and cross-metathesis Tetrahedron Letters. 45: 2447-2451. DOI: 10.1016/J.TETLET.2004.01.036 |
0.489 |
|
| 2003 |
Yao Q, Kinney EP, Yang Z. Ligand-free Heck reaction: Pd(OAc)2 as an active catalyst revisited. The Journal of Organic Chemistry. 68: 7528-31. PMID 12968913 DOI: 10.1021/Jo034646W |
0.5 |
|
| 2003 |
Yao Q, Zhang Y. Olefin metathesis in the ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate using a recyclable Ru catalyst: remarkable effect of a designer ionic tag. Angewandte Chemie (International Ed. in English). 42: 3395-8. PMID 12888968 DOI: 10.1002/anie.200351222 |
0.415 |
|
| 2002 |
Yao Q. OsO(4) in ionic liquid [Bmim]PF(6): a recyclable and reusable catalyst system for olefin dihydroxylation. remarkable effect of DMAP. Organic Letters. 4: 2197-9. PMID 12074666 DOI: 10.1021/Ol026172D |
0.606 |
|
| 2002 |
Yao Q. Synthesis of cyclic sulfones by ring-closing metathesis. Organic Letters. 4: 427-30. PMID 11820896 DOI: 10.1021/Ol017142Y |
0.471 |
|
| 2001 |
Yao Q. Rapid assembly of structurally defined and highly functionalized conjugated dienes via tethered enyne metathesis. Organic Letters. 3: 2069-72. PMID 11418051 DOI: 10.1021/Ol016026S |
0.506 |
|
| 2000 |
Yao Q. A Soluble Polymer-Bound Ruthenium Carbene Complex: A Robust and Reusable Catalyst for Ring-Closing Olefin Metathesis. Angewandte Chemie (International Ed. in English). 39: 3896-3898. PMID 29711712 DOI: 10.1002/1521-3773(20001103)39:21<3896::AID-ANIE3896>3.0.CO;2-8 |
0.436 |
|
| 1996 |
Crich D, Jiao X, Yao Q, Harwood JS. Radical Clock Reactions under Pseudo-First-Order Conditions Using Catalytic Quantities of Diphenyl Diselenide. A77Se- and119Sn-NMR Study of the Reaction of Tributylstannane and Diphenyl Diselenide The Journal of Organic Chemistry. 61: 2368-2373. DOI: 10.1021/Jo950857S |
0.343 |
|
| 1995 |
Crich D, Yao Q. Inhibition of Rearrangements in Stannane-Mediated Radical Reduction Reactions by Catalytic Quantities of Diphenyl Diselenide. An Example of Polarity Reversal Catalysis The Journal of Organic Chemistry. 60: 84-88. DOI: 10.1021/Jo00106A018 |
0.369 |
|
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