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Iron(III)/NaBH4-mediated additions to unactivated alkenes: synthesis of novel 20'-vinblastine analogues.
Org Lett. 2012 Mar 16;14(6):1428-31. doi: 10.1021/ol300173v. Epub 2012 Feb 28.
2
Fe(III)/NaBH4-mediated free radical hydrofluorination of unactivated alkenes.
J Am Chem Soc. 2012 Aug 22;134(33):13588-91. doi: 10.1021/ja3063716. Epub 2012 Aug 7.
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Iron-catalysed, general and operationally simple formal hydrogenation using Fe(OTf)3 and NaBH4.
Org Biomol Chem. 2014 Jul 28;12(28):5082-8. doi: 10.1039/c4ob00945b.
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Nitrous oxide reduction-coupled alkene-alkene coupling catalysed by metalloporphyrins.
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New insights into the mechanism and an expanded scope of the Fe(III)-mediated vinblastine coupling reaction.
J Am Chem Soc. 2012 Aug 15;134(32):13240-3. doi: 10.1021/ja306229x. Epub 2012 Aug 7.
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Rhodium(III)-Catalyzed Anti-Markovnikov Hydroamidation of Unactivated Alkenes Using Dioxazolones as Amidating Reagents.
J Am Chem Soc. 2022 Dec 14;144(49):22426-22432. doi: 10.1021/jacs.2c10552. Epub 2022 Dec 1.
9
Iron-mediated radical halo-nitration of alkenes.
J Org Chem. 2010 Dec 3;75(23):8126-32. doi: 10.1021/jo101769d. Epub 2010 Nov 10.
10
Fe-Catalyzed Olefin Hydroamination with Diazo Compounds for Hydrazone Synthesis.
Org Lett. 2016 Jan 4;18(1):128-31. doi: 10.1021/acs.orglett.5b03317. Epub 2015 Dec 14.

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Photocatalytic anti-Markovnikov hydro- and haloazidation of alkenes.
Nat Commun. 2025 Aug 25;16(1):7906. doi: 10.1038/s41467-025-63203-w.
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Iron-catalyzed radical Markovnikov hydrohalogenation and hydroazidation of alkenes.
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Metal-Hydride C-C Cross-Coupling of Alkenes Through a Double Outer-Sphere Mechanism.
J Org Chem. 2024 Nov 15;89(22):16106-16113. doi: 10.1021/acs.joc.4c00260. Epub 2024 Jun 26.
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Directed Hydrogen Atom Transfer for Selective Reactions of Polyenols.
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Fe/Thiol Cooperative Hydrogen Atom Transfer Olefin Hydrogenation: Mechanistic Insights That Inform Enantioselective Catalysis.
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Advancements in hydrochlorination of alkenes.
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Alkene Hydrobenzylation by a Single Catalyst That Mediates Iterative Outer-Sphere Steps.
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Inner- and Outer-Sphere Cross-Coupling of High F3 Fragments.
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本文引用的文献

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Catharanthine C16 substituent effects on the biomimetic coupling with vindoline: preparation and evaluation of a key series of vinblastine analogues.
Bioorg Med Chem Lett. 2010 Nov 15;20(22):6408-10. doi: 10.1016/j.bmcl.2010.09.091. Epub 2010 Sep 19.
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Asymmetric total synthesis of vindorosine, vindoline, and key vinblastine analogues.
J Am Chem Soc. 2010 Sep 29;132(38):13533-44. doi: 10.1021/ja106284s.
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Total synthesis and evaluation of a key series of C5-substituted vinblastine derivatives.
J Am Chem Soc. 2010 Jun 23;132(24):8489-95. doi: 10.1021/ja1027748.
5
Asymmetric total synthesis of vindoline.
J Am Chem Soc. 2010 Mar 24;132(11):3685-7. doi: 10.1021/ja910695e.
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Iron-mediated radical nitro-cyclization reaction of 1,6-dienes.
Org Lett. 2010 Jan 1;12(1):124-6. doi: 10.1021/ol902510p.
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Iron-catalyzed redox radical cyclizations of 1,6-dienes and enynes.
Org Lett. 2010 Jan 1;12(1):112-5. doi: 10.1021/ol902562j.
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Catalytic hydrochlorination of unactivated olefins with para-toluenesulfonyl chloride.
Angew Chem Int Ed Engl. 2008;47(31):5758-60. doi: 10.1002/anie.200801760.

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