Laura Furst

Affiliations: 
2008-2013 Chemistry Boston University, Boston, MA, United States 
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"Laura Furst"
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http://gradworks.umi.com/35/64/3564124.html

Mean distance: 8.76
 
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Parents

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Corey R.J. Stephenson grad student 2008-2013 Boston University
 (Radical-mediated heterocycle functionalization: Methodology development and natural product synthesis.)
Andrew J. Phillips post-doc 2013-2014 Yale
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Publications

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Eaton JK, Furst L, Cai LL, et al. (2020) Structure-activity relationships of GPX4 inhibitor warheads. Bioorganic & Medicinal Chemistry Letters. 127538
Eaton JK, Furst L, Ruberto RA, et al. (2020) Selective covalent targeting of GPX4 using masked nitrile-oxide electrophiles. Nature Chemical Biology
Sevrin MJ, Furst L, Nguyen JD, et al. (2018) Lithium bis-catechol borate as an effective reductive quencher in photoredox catalysis. Tetrahedron. 74: 3246-3252
Lofstrand VA, Matsuura BS, Furst L, et al. (2016) Formation and Trapping of Azafulvene Intermediates Derived from Manganese-Mediated Oxidative Malonate Coupling. Tetrahedron. 72: 3775-3780
Haftchenary S, Nelson SD, Furst L, et al. (2016) Efficient Routes to a Diverse Array of Amino Alcohol-Derived Chiral Fragments. Acs Combinatorial Science
Furst L, Stephenson CRJ. (2014) Gliocladin C: The development and application of a pyrroloindoline-indole radical coupling reaction Strategies and Tactics in Organic Synthesis. 10: 207-224
Freeman DB, Furst L, Condie AG, et al. (2012) Functionally diverse nucleophilic trapping of iminium intermediates generated utilizing visible light. Organic Letters. 14: 94-7
Furst L, Stephenson CR. (2011) Reaction design: Nature-inspired total synthesis. Nature Chemical Biology. 7: 582-3
Furst L, Narayanam JM, Stephenson CR. (2011) Total synthesis of (+)-gliocladin C enabled by visible-light photoredox catalysis. Angewandte Chemie (International Ed. in English). 50: 9655-9
Furst L, Narayanam JMR, Stephenson CRJ. (2011) Synthesis of (+)-Gliocladin C Synfacts. 2011: 1268-1268
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