Rauful Alam
Affiliations: | University of Pennsylvania, Philadelphia, PA, United States |
Area:
Organic ChemistryGoogle:
"http://rauful-alam.blogspot.com/"Mean distance: (not calculated yet)
Parents
Sign in to add mentorKálmán J. Szabó | grad student | 2012-2016 | Stockholm University |
Gary A. Molander | post-doc | 2016- | Penn |
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Publications
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Yi J, Badir SO, Alam R, et al. (2019) Photoredox-Catalyzed Multicomponent Petasis Reaction with Alkyltrifluoroborates. Organic Letters |
Molander G, Matsui J, Gutierrez-Bonet A, et al. (2018) Photoredox/Nickel-Catalyzed Single-Electron Tsuji-Trost Reaction: Development and Mechanistic Insight. Angewandte Chemie (International Ed. in English) |
Alam R, Molander GA. (2018) Photoredox-catalyzed Direct Reductive Amination of Aldehydes without an External Hydrogen/Hydride Source. Organic Letters |
Alam R, Molander GA. (2017) Direct Synthesis of Secondary Benzylic Alcohols Enabled by Photoredox/Ni Dual-Catalyzed Cross-Coupling. J Org Chem |
Amani J, Alam R, Badir S, et al. (2017) Synergistic Visible-Light Photoredox/Nickel-Catalyzed Synthesis of Aliphatic Ketones via N-C Cleavage of Imides. Organic Letters |
Alam R, Diner C, Jonker S, et al. (2016) Catalytic Asymmetric Allylboration of Indoles and Dihydroisoquinolines with Allylboronic Acids: Stereodivergent Synthesis of up to Three Contiguous Stereocenters. Angewandte Chemie (International Ed. in English) |
Miralles N, Alam R, Szabó KJ, et al. (2016) Transition-Metal-Free Borylation of Allylic and Propargylic Alcohols. Angewandte Chemie (International Ed. in English). 55: 4303-7 |
Alam R, Vollgraff T, Eriksson L, et al. (2015) Synthesis of Adjacent Quaternary Stereocenters by Catalytic Asymmetric Allylboration. Journal of the American Chemical Society. 137: 11262-5 |
Das A, Alam R, Eriksson L, et al. (2014) Stereocontrol in synthesis of homoallylic amines. Syn selective direct allylation of hydrazones with allylboronic acids. Organic Letters. 16: 3808-11 |
Alam R. (2014) Stereoselective allylboration of imines and indoles under mild conditions. An in situ E/Z isomerization of imines by allylboroxines Chemical Science |