Search Results - "Hatcher, Mark A"

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  1. 1

    Preparation of Methyltriazolo[1,4]benzodiazepine via Oxidative Activation of a Thiolactam for the Synthesis of BET Inhibitor Molibresib by Erickson, Greg A, Hatcher, Mark A, Journet, Michel, Kowalski, John A, Lovelace, Tom C, Pink, Christopher J, Xie, Shiping

    Published in Journal of organic chemistry (18-02-2022)
    “…A novel oxidative activation of a thiolactam was developed for the preparation of methyltriazolo[1,4]benzodiazepine in a single step. A sulfenic acid (R-SOH)…”
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  2. 2

    Copper-Catalyzed Asymmetric Hydrogenation of Aryl and Heteroaryl Ketones by Krabbe, Scott W, Hatcher, Mark A, Bowman, Roy K, Mitchell, Mark B, McClure, Michael S, Johnson, Jeffrey S

    Published in Organic letters (06-09-2013)
    “…High throughput screening enabled the development of a Cu-based catalyst system for the asymmetric hydrogenation of prochiral aryl and heteroaryl ketones that…”
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    New Silicon-Mediated, Sequential Ring Expansions of n-Sized 2-Cycloalkenones into Hydroxyolefinic n + m + p Medium-Sized Lactones:  Short Synthesis of (−)-Phoracantholide-J by Posner, Gary H, Hatcher, Mark A, Maio, William A

    Published in Organic letters (15-09-2005)
    “…In only four steps from 2-cyclopentenone and 2-cyclohexenone, sequential three- or four-atom and then one- to three-atom ring enlargements produce nine- to…”
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    Copper and silicon mediated, HMPA-free, n+3 ring expansions for the construction of medium sized lactones and lactams: short synthesis of (+)-cis-lauthisan by Posner, Gary H., Hatcher, Mark A., Maio, William A.

    Published in Tetrahedron (06-10-2016)
    “…In this report, several new epoxide examples were united with β-silyl ketone enolates for the construction, after oxidative fragmentation, of ring expanded…”
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  9. 9

    [3,3]-Sigmatropic rearrangements: short, stereocontrolled syntheses of functionalized vitamin D 3 side-chain units by Hatcher, Mark A, Posner, Gary H

    Published in Tetrahedron letters (08-07-2002)
    “…Enantiomerically pure C,D-ring allylic alcohol 4 stereospecifically undergoes five types of [3,4]-sigmatropic rearrangements to give C-23 functionalized 16-ene…”
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  10. 10

    New silicon-mediated ring expansion of n-sized conjugated cycloalkenones into homoallylic n+3 lactones by Hatcher, Mark A., Borstnik, Kristina, Posner, Gary H.

    Published in Tetrahedron letters (14-07-2003)
    “…Silicon nucleophilic β-addition to various 2-cycloalkenones, followed ultimately by mild and rapid α-alkylation of the corresponding cycloalkanone enolates…”
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  11. 11

    A-ring hydroxymethyl 19-nor analogs of the natural hormone 1alpha,25-dihydroxyvitamin D(3): synthesis and preliminary biological evaluation by Hatcher, Mark A, Peleg, Sara, Dolan, Patrick, Kensler, Thomas W, Sarjeant, Amy, Posner, Gary H

    Published in Bioorganic & medicinal chemistry (02-06-2005)
    “…A series 5-8 of 1- and 3-CH(2)OH 19-nor analogs of the hormone calcitriol (1) has been prepared. Surprisingly, 19-nor 1alpha-CH(2)OH analog 5a is more…”
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  12. 12

    A-ring hydroxymethyl 19-nor analogs of the natural hormone 1α,25-dihydroxyvitamin D 3: synthesis and preliminary biological evaluation by Hatcher, Mark A., Peleg, Sara, Dolan, Patrick, Kensler, Thomas W., Sarjeant, Amy, Posner, Gary H.

    Published in Bioorganic & medicinal chemistry (02-06-2005)
    “…[Display omitted] A series 5– 8 of 1- and 3-CH 2OH 19-nor analogs of the hormone calcitriol ( 1) has been prepared. Surprisingly, 19-nor 1α-CH 2OH analog 5a is…”
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    Journal Article
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