112. "Studies toward the Synthesis of Amphidinolide C1: Stereoselective Construction of the C(1)–C(15) Segment"
Namirembe, S.; Yan, L.; Morken, J. P. Org. Lett. 2020, 22, 9174–9177. DOI: 10.1021/acs.orglett.0c03134.
111. "Diastereo- and Enantioselective 1,4-Difunctionalization of Borylenynes by Catalytic Conjunctive Cross-Coupling"
Law, C.; Kativhu, E.; Wang, J.; Morken, J. P. Angew. Chem. Int. Ed. 2020, 59, 10311–10315, DOI: 10.1002/anie.202001580.
110. "Catalytic Enantioselective Synthesis of Anti-Vicinal Silylboronates by Conjunctive Cross-Coupling"
Meng, Y.; Kong, Z.; Morken, J. P. Angew. Chem. Int. Ed. 2020, 59, 8456–8459, DOI: /10.1002/anie.202000937.
109. "Alkyl Group Migration in Ni-Catalyzed Conjunctive Coupling with C(sp3) Electrophiles: Reaction Development and Application to Targets of Interest"
Koo, S. M.; Vendola, A. J.; Momm, S. N.; Morken, J. P. Org. Lett. 2020, 22, 666–669. DOI: 10.1021/acs.orglett.9b04453.
108. "Recent Advances in Radical Addition to Alkenylboron Compounds"
Lovinger, G. J.; Morken, J. P. Eur. J. Org. Chem. 2020, 2362–2368. DOI: 10.1002/ejoc.201901600.
107. "Catalytic Enantioselective Synthesis of β-Allenyl Boronic Esters by Conjunctive Cross-Coupling with Propargylic Carbonates"
Aparece, M. D.; Hu, W.; Morken, J. P. Acs. Catal. 2019, 9, 11381–11385. DOI: 10.1021/acscatal.9b04453.
106. "Enantioselective Radical Addition/Cross‐Coupling of Organozinc Reagents, Alkyl Iodides, and Alkenylboron Reagents"
Chierchia, M.; Xu, P.; Lovinger, G. J.; Morken, J. P. Angew. Chem. Int. Ed. 2019, 58, 14245–14249. DOI: 10.1002/anie.201908029.
105. "Stereoselective Synthesis of Trisubstituted Alkenylboron Reagents by Boron-Wittig Reaction of Ketones"
Namirembe, S.; Gao, C.; Wexler, R. P.; Morken, J. P. Org. Lett. 2019, 21, 4392–4394. DOI: 10.1021/acs.orglett.9b01663.
104. "Reactions of Organoboron Compounds Enabled by Catalyst-Promoted Metalate Shifts"
Namirembe, S.; Morken, J. P. Chem. Soc. Rev. 2019, 48, 3464–3474, DOI: 10.1039/C9CS00180H.
103. "Site-Selective Mono-Oxidation of 1,2-Bis(boronates)"
Yan, L.; Morken, J. P. Org. Lett. 2019, 21, 3760–3763. DOI: 10.1021/acs.orglett.9b01204.
102. "Catalytic Conjunctive Coupling of Carboxylic Acid Derivatives with 9-BBN-Derived Ate Complexes"
Law, C.; Meng, Y.; Koo, S. M.; Morken, J. P. Angew. Chem. Int. Ed. 2019, 58, 6654–6658. DOI: 10.1002/anie.201901927.
101. "Vinylidenation of Organoboronic Esters Enabled by a Pd- Catalyzed Metallate Shift"
Aparece, M. D.; Gao, C.; Lovinger, G. J.; Morken, J. P. Angew. Chem. Int. Ed. 2019, 58, 592–595. DOI: 10.1002/anie.201811782.
100. "Diastereoselective and Enantioselective Conjunctive Cross-Coupling Enabled by Boron Ligand Design"
Myhill, J. A.; Wilhelmsen, C. A.; Zhang, L.; Morken, J. P. J. Am. Chem. Soc. 2018, 140, 15181–15185. DOI: 10.1021/jacs.8b09909.
99. "Enantioselective Construction of Tertiary Boronic Esters by Conjunctive Cross‐Coupling"
Myhill, J. A.; Zhang, L.; Lovinger, G. J.; Morken, J. P. Angew. Chem. Int. Ed. 2018, 57, 12799–12803. DOI: 10.1002/anie.201807775.
98. "A Protocol for Direct Stereospecific Amination of Primary, Secondary, and Tertiary Alkylboronic Esters"
Edelstein, E. K.; Grote, A. C.; Palkowitz, M. D.; Morken, J. P. Synlett 2018, 29, 1749–1752. DOI: 10.1055/s-0037-1610172.
97. "Synthesis and Stereochemical Assignment of Arenolide"
Liu, X.; Sun, C.; Mlynarski, S.; Morken, J. P. Org. Lett. 2018, 20, 1898–1901. DOI: 10.1021/acs.orglett.8b00439
96. "Carbohydrate/DBU Cocatalyzed Alkene Diboration: Mechanistic Insight Provides Enhanced Catalytic Efficiency and Substrate Scope"
Yan, L.; Meng, Y.; Haeffner, F.; Leon, R. M.; Crockett, M. P.; Morken, J. P. J. Am. Chem. Soc. 2018, 140, 3663–3673. DOI: 10.1021/jacs.7b12316.
95. "Enantioselective Synthesis of Nonracemic Geminal Silylboronates by Pt-Catalyzed Hydrosilylation"
Szymaniak, A. A.; Zhang, C.; Coombs, J. R.; Morken, J. P.; ACS Catal. 2018, 8, 2897–2901. DOI: 10.1021/acscatal.8b00221.
94. "Ni-Catalyzed Enantioselective Conjunctive Coupling with C(sp3) Electrophiles: A Radical-Ionic Mechanistic Dichotomy"
Lovinger, G. J.; Morken, J. P.; J. Am. Chem. Soc. 2017, 139, 17293–17296. DOI: 10.1021/jacs.7b10519.
93. "Ni-Catalyzed Enantioselective Conjunctive Cross-Coupling of 9-BBN Borates"
Chierchia, M.; Law, C.; Morken, J. P. Angew. Chem. Int. Ed. 2017, 56, 1870–11874. DOI: 10.1002/anie.201706719.
92. "A Boron Alkylidene-Alkene Cycloaddition Reaction: Application to the Synthesis of Aphanamal"
Liu, X.; Deaton, T. M.; Haeffner, F.; Morken, J. P.; Angew. Chem. Int. Ed. 2017, 56, 11485–11489. DOI: 10.1002/anie.201705720.
91. "Enantioselective Conjunctive Cross-Coupling of Bis(alkenyl) Borates: A General Synthesis of Chiral Allylboron Reagents"
Edelstein, K. E.; Namirembe, S.; Morken, J. P.; J. Am. Chem. Soc. 2017, 139, 5027–5030. DOI: 10.1021/jacs.7b01774.
90. "Pd-Catalyzed Conjunctive Cross-Coupling Between Grignard-Derived Boron "Ate" Complexes and C(sp2) Halides or Triflates: NaOTf as a Grignard Activator and Halide Scavenger"
Lovinger, G. J.; Aparece, M. D.; Morken, J. P. J. Am. Chem. Soc. 2017, 139, 3153–3160. DOI: 10.1021/jacs.6b12663.
89. "Modular, Catalytic Enantioselective Construction of Quaternary Carbon Stereocenters by Sequential Cross-Coupling Reactions"
Potter, B.; Edelstein, E. K.; Morken, J. P. Org. Lett., 2016, 18, 3286–3289. DOI: 10.1021/acs.orglett.6b01580.
88. "Nickel-Catalyzed Asymmetric Kumada Cross-Coupling of Symmetric Cyclic Sulfates"
Eno, M. S.; Lu, A.; Morken, J. P. J. Am. Chem. Soc. 2016, 138, 7824–7827. DOI: 10.1021/jacs.6b03384.
87. "Carbohydrate-Catalyzed Enantioselective Alkene Diboration: Enhanced Reactivity of 1,2-Bonded Diboron Complexes"
Fang, L.; Yan, L.; Haeffner, F.; Morken, J. P. J. Am. Chem. Soc. 2016, 138, 2508–2511. DOI: 0.1021/jacs.5b13174.
86. "Catalytic Enantioselective Functionalization of Unactivated Terminal Alkenes"
Coombs. J. R.; Morken, J. P. Angew. Chem. Int. Ed. 2016, 55, 2636–2649. DOI: 10.1002/anie.201507151.
85. "Catalytic conjunctive cross-coupling enabled by metal-induced metallate rearrangement"
Zhang, L.; Lovinger, G. J.; Edelstein, E. K.; Szymaniak, A. A.; Chierchia, M. P.; Morken, J. P. Science, 2016, 351, 70–74. DOI: 10.1126/science.aad6080.