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Steven A Loskot

Explore the profile of Steven A Loskot including associated specialties, affiliations and a list of published articles. Areas
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Articles 8
Citations 98
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Recent Articles
1.
Hafeman N, Loskot S, Reimann C, Pritchett B, Virgil S, Stoltz B
Chem Sci . 2023 May; 14(18):4745-4758. PMID: 37181769
The complete account of the total syntheses of scabrolide A and yonarolide is disclosed. This article describes an initial approach involving a bio-inspired macrocyclization/transannular Diels-Alder cascade, which ultimately failed due...
2.
Hafeman N, Chan M, Fulton T, Alexy E, Loskot S, Virgil S, et al.
J Am Chem Soc . 2022 Oct; 144(44):20232-20236. PMID: 36287147
The first total synthesis of the furanobutenolide-derived cembranoid diterpenoid havellockate is disclosed. Our convergent strategy employs a Julia-Kocienski olefination to join two enantioenriched fragments to produce a diene that is...
3.
Zhang T, Cusumano A, Hafeman N, Loskot S, Reimann C, Virgil S, et al.
J Org Chem . 2022 Oct; 87(21):14115-14124. PMID: 36269312
We utilize ab initio quantum mechanics calculations to evaluate a range of plausible mechanistic pathways for the unexpected formation of a [6-4-4] ring system from an enone-olefin photocycloaddition in the...
4.
Hafeman N, Loskot S, Reimann C, Pritchett B, Virgil S, Stoltz B
J Am Chem Soc . 2020 Apr; 142(19):8585-8590. PMID: 32223255
The first total synthesis of the norcembranoid diterpenoid scabrolide A is disclosed. The route begins with the synthesis of two chiral pool-derived fragments, which undergo a convergent coupling to expediently...
5.
Loskot S, Romney D, Arnold F, Stoltz B
J Am Chem Soc . 2017 Jul; 139(30):10196-10199. PMID: 28721734
An enantioselective total synthesis of the norditerpenoid alkaloid nigelladine A is described. Strategically, the synthesis relies on a late-stage C-H oxidation of an advanced intermediate. While traditional chemical methods failed...
6.
Craig 2nd R, Loskot S, Mohr J, Behenna D, Harned A, Stoltz B
Org Lett . 2015 Oct; 17(21):5160-3. PMID: 26501770
The first general method for the enantioselective construction of all-carbon quaternary centers on cyclopentanones by enantioselective palladium-catalyzed decarboxylative allylic alkylation is described. Employing the electronically modified (S)-(p-CF3)3-t-BuPHOX ligand, α-quaternary cyclopentanones...
7.
Loskot S, Zhang J, Langenhan J
J Org Chem . 2013 Nov; 78(23):12189-93. PMID: 24180591
Neoglycosylations are increasingly being employed in the synthesis of natural products, drug candidates, glycopeptide mimics, oligosaccharide analogues, and other applications, but the efficiency of these reactions is usually limited by...
8.
Langenhan J, Mullarky E, Rogalsky D, Rohlfing J, Tjaden A, Werner H, et al.
J Org Chem . 2013 Feb; 78(4):1670-6. PMID: 23368752
The amphimedosides, discovered in 2006, are the first examples of naturally occurring glycosylated alkoxyamines. We report syntheses of amphimedosides A-C that feature a stereoselective oxyamine neoglycosylation and found that these...