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The Herzon Group
Yale University, New Haven, CT  
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Dr. Seth B. Herzon
Chemistry Research Building
Room 116
seth.herzon@yale.edu

Office: 203.436.8571
Lab: 203.432.8572

Mail:
Yale University
Department of Chemistry
PO Box 208107
New Haven, CT 06520-8107

Shipping:
Yale University
Department of Chemistry
350 Edwards St.
New Haven, CT 06511

 
Publications
  1. 2-Azabicyclo[2.1.1]hexanes. 2. Substituent Effects on the Bromine-Mediated
    Rearrangement of 2-Azabicyclo[2.2.0]hex-5-enes. Grant R. Krow, Yoon B. Lee,
    Walden S. Lester, Nian Liu, Jing Yuan, Jinqi Duo, Seth B. Herzon, Yen Nguyen,
    and David Zacharias, J. Org. Chem. 2001, 66, 1805.
  2. Synthesis of Novel 2-Azabicyclo[2.2.0]- and [2.1.1]hexanols. Grant R. Krow, Walden S.
    Lester, Nian Liu, Jing Yuan, Amanda Hiller, Jinqi Duo, Seth B. Herzon, Yen Nguyen,
    and Kevin Cannon, J. Org. Chem. 2001, 66, 1811.
  3. Complex-Induced Proximity Effects. Temperature-Dependent Regiochemical Diversity
    in Lithiation-Electrophilic Substitution Reactions of N-Boc-2-Azabicyclo[2.1.1]hexane.
    2,4- and 3,5-Methanoprolines. Grant R. Krow, Seth B. Herzon, Gouliang Lin, Feng Qiu,
    and Philip E. Sonnet, Org. Lett. 2002, 4, 3151.
  4. The Rearrangement Route to 2-Azabicyclo[2.1.1]hexanes. Solvent and Electrophile
    Control of Neighboring Group Participation. Grant R. Krow, Gouliang Lin, Deepa
    Rapolu, Yuhong Fang, Walden S. Lester, Seth B. Herzon, and Philip E. Sonnet, J. Org.
    Chem.
    2003, 68, 5292.
  5. Convenient Preparations of 2,4-Methanopyrrolidine and 5-Carboxy-2,4-
    methanopyrrolidines. Grant R. Krow, Guoliang Lin, Seth B. Herzon, Andrew M.
    Thomas, Keith P. Moore, Qiuli Huang, and Patrick J. Carroll, J. Org. Chem. 2003, 68,
    7562.
  6. Identification of a Novel Michael Acceptor Group for the Reversible Addition of
    Oxygen- and Sulfur-Based Nucleophiles. Synthesis and Reactivity of the 3-Alkylidene-
    3H-indole 1-Oxide Function of Avrainvillamide. Andrew G. Myers and Seth B. Herzon,
    J. Am. Chem. Soc. 2003, 125, 12080.
  7. Enantioselective Synthesis of Stephacidin B. Seth B. Herzon and Andrew G. Myers, J.
    Am. Chem. Soc.
    2005, 127, 5342.
  8. Evidence for the Rapid Conversion of Stephacidin B into the Electrophilic Monomer
    Avrainvillamide in Cell Culture. Jeremy E. Wulff, Seth B. Herzon, Romain Siegrist,
    and Andrew G. Myers, J. Am. Chem. Soc. 2007, 129, 4898.
  9. Direct, Catalytic Hydroaminoalkylation of Unactivated Olefins with N-alkyl Arylamines.
    Seth B. Herzon and John F. Hartwig, J. Am. Chem. Soc. 2007, 129, 6690.
  10. Hydroaminoalkylation of Unactivated Olefins with Dialkylamines.
    Seth B. Herzon and John F. Hartwig, J. Am. Chem. Soc. 2008, 130, 14940.

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