Works matching AU Reisman, Sarah E.
Results: 19
Electrochemical Preparation of Sm(II) Reagent Facilitated by Weakly Coordinating Anions.
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- Chemistry - A European Journal, 2023, v. 29, n. 46, p. 1, doi. 10.1002/chem.202301045
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Nickel‐Catalyzed Reductive Alkylation of Heteroaryl Imines.
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- Angewandte Chemie, 2022, v. 134, n. 38, p. 1, doi. 10.1002/ange.202207597
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Enantioselective Synthesis of (−)‐10‐Hydroxyacutuminine.
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- Angewandte Chemie, 2022, v. 134, n. 16, p. 1, doi. 10.1002/ange.202117480
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Plugging the Leak: Empowering Women in Organic Chemistry.
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- Angewandte Chemie, 2022, v. 134, n. 5, p. 1, doi. 10.1002/ange.202111765
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Nickel‐Catalyzed Conversion of Enol Triflates into Alkenyl Halides.
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- Angewandte Chemie, 2019, v. 131, n. 42, p. 15043, doi. 10.1002/ange.201906815
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Medicinal chemistry: New lead for pain treatment.
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- Nature, 2011, v. 473, n. 7348, p. 458, doi. 10.1038/473458a
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Short, Enantioselective Total Syntheses of (−)-8-Demethoxyrunanine and (−)-Cepharatines A, C, and D.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 40, p. 9447, doi. 10.1002/anie.201104487
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Organic chemistry: Single molecules put a ring on it.
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- Nature, 2012, v. 490, n. 7419, p. 179, doi. 10.1038/490179a
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Nickel‐Catalyzed Reductive Alkylation of Heteroaryl Imines.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 38, p. 1, doi. 10.1002/anie.202207597
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- Article
Enantioselective Synthesis of (−)‐10‐Hydroxyacutuminine.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 16, p. 1, doi. 10.1002/anie.202117480
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- Article
Plugging the Leak: Empowering Women in Organic Chemistry.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 5, p. 1, doi. 10.1002/anie.202111765
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- Publication type:
- Article
Nickel‐Catalyzed Conversion of Enol Triflates into Alkenyl Halides.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 42, p. 14901, doi. 10.1002/anie.201906815
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- Article
Short, Enantioselective Total Syntheses of (−)-8-Demethoxyrunanine and (−)-Cepharatines A, C, and D.
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- Angewandte Chemie, 2011, v. 123, n. 40, p. 9619, doi. 10.1002/ange.201104487
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A Mild and Efficient Synthesis of Oxindoles: Progress Towards the Synthesis of Welwitindolinone A Isonitrile ( We gratefully acknowledge financial support from Yamanouchi, Merck, Pfizer, and Amgen. J.M.R. is the recipient of an NIH postdoctoral fellowship. K.R. thanks Sankyo Co., LTD.; M.H. thanks Daiso Co., LTD., M.M.W. thanks Bristol Myers Squibb for a graduate fellowship. )
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- Angewandte Chemie, 2004, v. 116, n. 10, p. 1290
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Synthesis of Enantioenriched Indolines by a Conjugate Addition/Asymmetric Protonation/Aza-Prins Cascade Reaction.
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- Angewandte Chemie, 2016, v. 128, n. 10, p. 3459, doi. 10.1002/ange.201510972
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Enantioselective Total Synthesis of (−)-Lansai B and (+)-Nocardioazines A and B.
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- Angewandte Chemie, 2014, v. 126, n. 24, p. 6320, doi. 10.1002/ange.201402571
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A Mild and Efficient Synthesis of Oxindoles: Progress Towards the Synthesis of Welwitindolinone A Isonitrile ( We gratefully acknowledge financial support from Yamanouchi, Merck, Pfizer, and Amgen. J.M.R. is the recipient of an NIH postdoctoral fellowship. K.R. thanks Sankyo Co., LTD.; M.H. thanks Daiso Co., LTD., M.M.W. thanks Bristol Myers Squibb for a graduate fellowship. )
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- Angewandte Chemie International Edition, 2004, v. 43, n. 10, p. 1270, doi. 10.1002/anie.200353282
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Synthesis of Enantioenriched Indolines by a Conjugate Addition/Asymmetric Protonation/Aza-Prins Cascade Reaction.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 10, p. 3398, doi. 10.1002/anie.201510972
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Enantioselective Total Synthesis of (−)-Lansai B and (+)-Nocardioazines A and B.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 24, p. 6206, doi. 10.1002/anie.201402571
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