Year |
Citation |
Score |
2022 |
Kuang Q, Hu X, Li Y, Shang S, Huang X, Liao S, Song Y, Ma W, Li S, Liu A, Liu X, Zhang X, Yuan J. A rapid construction of new boron heterocycles and evaluation of photophysical properties of iminoboronates. Organic & Biomolecular Chemistry. PMID 35876433 DOI: 10.1039/d2ob01083f |
0.348 |
|
2021 |
Huang X, Zhang W. Recyclable fluorous cinchona organocatalysts for asymmetric synthesis of biologically interesting compounds. Chemical Communications (Cambridge, England). PMID 34522921 DOI: 10.1039/d1cc03722f |
0.359 |
|
2018 |
Huang X, Zhao W, Zhang X, Liu M, Vasconcelos SNS, Zhang W. One-pot Fluorination and Organocatalytic Robinson Annulation for Asymmetric Synthesis of Mono- and Difluorinated Cyclohexenones. Molecules (Basel, Switzerland). 23. PMID 30181479 DOI: 10.3390/molecules23092251 |
0.553 |
|
2016 |
Song Z, Huang X, Yi W, Zhang W. One-Pot Reactions for Modular Synthesis of Polysubstituted and Fused Pyridines. Organic Letters. PMID 27775367 DOI: 10.1021/acs.orglett.6b02883 |
0.361 |
|
2016 |
Huang X, Liu M, Pham K, Zhang X, Yi W, Jasinski JP, Zhang W. Organocatalytic One-pot Asymmetric Synthesis of Thiolated Spiro-gamma-lactam-oxindoles Bearing Three Stereocenters. The Journal of Organic Chemistry. PMID 27258150 DOI: 10.1021/Acs.Joc.6B00653 |
0.548 |
|
2015 |
Qian J, Yi W, Huang X, Miao Y, Zhang J, Cai C, Zhang W. One-pot synthesis of 3,5-disubstituted and polysubstituted phenols from acyclic precursors. Organic Letters. 17: 1090-3. PMID 25675098 DOI: 10.1021/ol503615n |
0.535 |
|
2013 |
Lu Q, Huang X, Song G, Sun CM, Jasinski JP, Keeley AC, Zhang W. Sequential [3 + 2] and [4 + 2] cycloadditions for stereoselective synthesis of a novel polyheterocyclic scaffold. Acs Combinatorial Science. 15: 350-5. PMID 23701651 DOI: 10.1021/Co400026S |
0.494 |
|
2012 |
Yi WB, Huang X, Zhang Z, Zhu DR, Cai C, Zhang W. Recyclable fluorous cinchona alkaloid ester as a chiral promoter for asymmetric fluorination of β-ketoesters. Beilstein Journal of Organic Chemistry. 8: 1233-40. PMID 23019453 DOI: 10.3762/Bjoc.8.138 |
0.568 |
|
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