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Armstrong, Megan K., Goodstein, Madison B., Lalic, Gojko (2018) Diastereodivergent Reductive Cross Coupling of Alkynes through Tandem Catalysis: Z- and E-Selective Hydroarylation of Terminal Alkynes. Journal Of The American Chemical Society, 140 (32) 10233-10241 doi:10.1021/jacs.8b05113

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Reference TypeJournal (article/letter/editorial)
TitleDiastereodivergent Reductive Cross Coupling of Alkynes through Tandem Catalysis: Z- and E-Selective Hydroarylation of Terminal Alkynes
JournalJournal Of The American Chemical Society
AuthorsArmstrong, Megan K.Author
Goodstein, Madison B.Author
Lalic, GojkoAuthor
Year2018 (August 15)Volume140
Issue32
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/jacs.8b05113Search in ResearchGate
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Mindat Ref. ID1799504Long-form Identifiermindat:1:5:1799504:7
GUID0
Full ReferenceArmstrong, Megan K., Goodstein, Madison B., Lalic, Gojko (2018) Diastereodivergent Reductive Cross Coupling of Alkynes through Tandem Catalysis: Z- and E-Selective Hydroarylation of Terminal Alkynes. Journal Of The American Chemical Society, 140 (32) 10233-10241 doi:10.1021/jacs.8b05113
Plain TextArmstrong, Megan K., Goodstein, Madison B., Lalic, Gojko (2018) Diastereodivergent Reductive Cross Coupling of Alkynes through Tandem Catalysis: Z- and E-Selective Hydroarylation of Terminal Alkynes. Journal Of The American Chemical Society, 140 (32) 10233-10241 doi:10.1021/jacs.8b05113
In(2018, August) Journal Of The American Chemical Society Vol. 140 (32) American Chemical Society (ACS)

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Armstrong, Megan K., Lalic, Gojko (2019) Differential Dihydrofunctionalization of Terminal Alkynes: Synthesis of Benzylic Alkyl Boronates through Reductive Three-Component Coupling. Journal Of The American Chemical Society, 141 (15) 6173-6179 doi:10.1021/jacs.9b02372
Lee, Mitchell T., Goodstein, Madison B., Lalic, Gojko (2019) Synthesis of Isomerically Pure (Z)-Alkenes from Terminal Alkynes and Terminal Alkenes: Silver-Catalyzed Hydroalkylation of Alkynes. Journal Of The American Chemical Society, 141 (43) 17086-17091 doi:10.1021/jacs.9b09336
Lee, Mitchell T., Lalic, Gojko (2021) Mechanism of Z-Selective Hydroalkylation of Terminal Alkynes. Journal of the American Chemical Society, 143 (40) 16663-16672 doi:10.1021/jacs.1c07613
Mailig, Melrose, Hazra, Avijit, Armstrong, Megan K., Lalic, Gojko (2017) Catalytic Anti-Markovnikov Hydroallylation of Terminal and Functionalized Internal Alkynes: Synthesis of Skipped Dienes and Trisubstituted Alkenes. Journal Of The American Chemical Society, 139 (20) 6969-6977 doi:10.1021/jacs.7b02104
Hazra, Avijit, Chen, Jason, Lalic, Gojko (2019) Stereospecific Synthesis of E-Alkenes through Anti-Markovnikov Hydroalkylation of Terminal Alkynes. Journal Of The American Chemical Society, 141 (32) 12464-12469 doi:10.1021/jacs.9b04800
Shaff, Austin B., Hazra, Avijit, Gardner, Bradley W., Lalic, Gojko (2025) Selective Synthesis of Z-Michael Acceptors via Hydroalkylation of Conjugated Alkynes. Journal of the American Chemical Society, 147 (1). doi:10.1021/jacs.4c09755
Uehling, Mycah R., Suess, Alison M., Lalic, Gojko (2015) Copper-Catalyzed Hydroalkylation of Terminal Alkynes. Journal Of The American Chemical Society, 137 (4) 1424-1427 doi:10.1021/ja5124368
Hazra, Avijit, Kephart, Jonathan A., Velian, Alexandra, Lalic, Gojko (2021) Hydroalkylation of Alkynes: Functionalization of the Alkenyl Copper Intermediate through Single Electron Transfer Chemistry. Journal of the American Chemical Society, 143 (21) 7903-7908 doi:10.1021/jacs.1c03396
Hazra, Avijit, Lee, Mitchell T., Chiu, Justin F., Lalic, Gojko (2018) Photoinduced Copper-Catalyzed Coupling of Terminal Alkynes and Alkyl Iodides. Angewandte Chemie, 130 (19). 5590-5594 doi:10.1002/ange.201801085
Uehling, Mycah R., Rucker, Richard P., Lalic, Gojko (2014) Catalytic Anti-Markovnikov Hydrobromination of Alkynes. Journal Of The American Chemical Society, 136 (24) 8799-8803 doi:10.1021/ja503944n
Hazra, Avijit, Lee, Mitchell T., Chiu, Justin F., Lalic, Gojko (2018) Photoinduced Copper-Catalyzed Coupling of Terminal Alkynes and Alkyl Iodides. Angewandte Chemie International Edition, 57 (19). 5492-5496 doi:10.1002/anie.201801085
 
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