Year |
Citation |
Score |
2020 |
Burde AS, Karyakarte SD, Sylvester ED, Chemler SR. Copper-catalyzed enantioselective synthesis of bridged bicyclic ketals from 1,1-disubstituted-4-methylene-1,6-hexanediols and related alkenols. Chemical Communications (Cambridge, England). PMID 33326512 DOI: 10.1039/d0cc06404a |
0.489 |
|
2018 |
Chemler SR, Karyakarte S, Um C, Berhane I. Synthesis of Spirocyclic Ethers Via Enantioselective Copper-Catalyzed Carboetherification of Alkenols. Angewandte Chemie (International Ed. in English). PMID 30117646 DOI: 10.1002/Anie.201808554 |
0.756 |
|
2018 |
Li G, Zatolochnaya OV, Wang XJ, Rodríguez S, Qu B, Desrosiers JN, Mangunuru HPR, Biswas S, Rivalti D, Karyakarte SD, Sieber JD, Grinberg N, Wu L, Lee H, Haddad N, et al. BABIPhos Family of Biaryl Dihydrobenzooxaphosphole Ligands for Asymmetric Hydrogenation. Organic Letters. PMID 29542928 DOI: 10.1021/Acs.Orglett.8B00139 |
0.366 |
|
2018 |
Qu B, Mangunuru HPR, Tcyrulnikov S, Rivalti D, Zatolochnaya OV, Kurouski D, Radomkit S, Biswas S, Karyakarte S, Fandrick KR, Sieber JD, Rodriguez S, Desrosiers JN, Haddad N, McKellop K, et al. Enantioselective Synthesis of α-(Hetero)aryl Piperidines through Asymmetric Hydrogenation of Pyridinium Salts and Its Mechanistic Insights. Organic Letters. PMID 29461064 DOI: 10.1021/Acs.Orglett.8B00067 |
0.427 |
|
2017 |
Chemler SR, Karyakarte S, Khoder ZM. Stereoselective and Regioselective Synthesis of Heterocycles Via Copper-Catalyzed Additions of Amine Derivatives and Alcohols to Alkenes. The Journal of Organic Chemistry. PMID 28910106 DOI: 10.1021/Acs.Joc.7B02072 |
0.743 |
|
2015 |
Karyakarte SD, Sequeira FC, Zibreg GH, Huang G, Matthew JP, Ferreira MM, Chemler SR. Copper-promoted synthesis of 1,4-benzodiazepinones via alkene diamination. Tetrahedron Letters. 56: 3686-3689. PMID 26034340 DOI: 10.1016/J.Tetlet.2015.01.171 |
0.632 |
|
2012 |
Karyakarte SD, Smith TP, Chemler SR. Stereoselective isoxazolidine synthesis via copper-catalyzed alkene aminooxygenation. The Journal of Organic Chemistry. 77: 7755-60. PMID 22870912 DOI: 10.1021/Jo3013226 |
0.681 |
|
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