Mason Hammond
#61,196
Most Influential Person Now
American educator and scholar
Mason Hammond's AcademicInfluence.com Rankings
Mason Hammondliterature Degrees
Literature
#2513
World Rank
#4438
Historical Rank
#1189
USA Rank
Classical Studies
#15
World Rank
#33
Historical Rank
#5
USA Rank

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Literature
Why Is Mason Hammond Influential?
(Suggest an Edit or Addition)According to Wikipedia, Mason Hammond was an American educator and scholar. He was a Harvard University professor, an authority on Latin and the history of Rome and its empire, and chairman of the board of trustees at St. Mark's School.
Mason Hammond's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Development of a small-molecule serum- and glucocorticoid-regulated kinase-1 antagonist and its evaluation as a prostate cancer therapeutic. (2008) (191)
- Synthetic aspects of an asymmetric nitrogen-insertion process: preparation of chiral, non-racemic caprolactams and valerolactams. Total synthesis of (-)-alloyohimbane (1990) (54)
- Development of an enantioselective synthetic route to neocarzinostatin chromophore and its use for multiple radioisotopic incorporation. (2002) (54)
- A mild, osmium tetraoxide-catalyzed method for the oxidation of sulfides to sulfones (1991) (48)
- TOTAL SYNTHESIS OF (+)-NEOCARZINOSTATIN CHROMOPHORE (1998) (44)
- ENANTIOSELECTIVE SYNTHESIS OF NEOCARZINOSTATIN CHROMOPHORE AGLYCON (1996) (37)
- Design and synthesis of orally bioavailable serum and glucocorticoid-regulated kinase 1 (SGK1) inhibitors. (2009) (37)
- Antioxidant-based inhibitors of leukotriene biosynthesis. The discovery of 6-[1-[2-(hydroxymethyl)phenyl]-1-propen-3-yl]-2,3-dihydro-5- benzofuranol, a potent topical antiinflammatory agent. (1990) (36)
- 2,3-Dihydro-5-benzofuranols as antioxidant-based inhibitors of leukotriene biosynthesis. (1989) (30)
- An Improved Preparation of Highly Enantiomerically Enriched (R)-(+)-4-tert-Butyldimethylsiloxy-2-cyclopenten-1-one. (1996) (28)
- Directed regiochemical control in the ring expansion reactions of a substituted trans-decalone (1990) (27)
- A Comparison of DNA Cleavage by Neocarzinostatin Chromophore and Its Aglycon: Evaluating the Role of the Carbohydrate Residue (1997) (26)
- In vitro and in vivo characterization of 3-[2-[6-(2-tert-butoxyethoxy)pyridin-3-yl]-1H-imidazol-4-yl]benzonitrile hydrochloride salt, a potent and selective NPY5 receptor antagonist. (2003) (25)
- Structure-activity relationship studies on 2-heteroaryl-4-arylimidazoles NPY5 receptor antagonists. (2003) (24)
- Syntheses and rearrangements of spirocyclic oxaziridines derived from unsymmetrical ketones (1991) (23)
- Structure-activity relationships in a series of NPY Y5 antagonists: 3-amido-9-ethylcarbazoles, core-modified analogues and amide isosteres. (2003) (14)
- A systematic study of P1–P3 spanning sidechains for the inhibition of HIV-1 protease (1995) (13)
- Synthesis and SAR of amino acid-derived heterocyclic progesterone receptor full and partial agonists. (2009) (11)
- Biochemical and biological activities of 2,3-dihydro-6-[3-(2-hydroxymethyl)phenyl-2-propenyl]-5-benzofuranol (L-651,896), a novel topical anti-inflammatory agent. (1987) (11)
- A Concise Synthesis of the Naphthoic Acid Component of Neocarzinostatin Chromophore Featuring a New Photocyclization Reaction (1996) (10)
- 2-Amino-9-aryl-3-cyano-4-methyl-7-oxo-6,7,8,9-tetrahydropyrido[2',3':4,5]thieno[2,3-b]pyridine derivatives as selective progesterone receptor agonists. (2009) (10)
- Improving the developability profile of pyrrolidine progesterone receptor partial agonists. (2010) (10)
- Bioisosteric replacement of the hydrazide pharmacophore of the cannabinoid-1 receptor antagonist SR141716A. Part I: potent, orally-active 1,4-disubstituted imidazoles. (2009) (9)
- Discovery of orally active, pyrrolidinone-based progesterone receptor partial agonists. (2009) (7)
- Synthetic replacement of the methylamino group of neocarzinostatin chromophore with hydroxyl prohibits thiol activation in organic solvents and diminishes the rate and efficiency of thiol-promoted DNA cleavage in water (1999) (6)
- ITERATIVE PROTEIN STRUCTURE-BASED DRUG DESIGN AND SYNTHESIS OF HIV PROTEASE INHIBITORS (1995) (6)
- Neuropeptide Y receptor antagonists. (2001) (4)
- An Improved Preparation of Highly Enantiomerically Enriched (R)-(+)-4- tert-Butyldimethylsiloxy-2-cyclopenten-1-one. (1996) (3)
- Total Synthesis of (+)‐Neocarzinostatin Chromophore. (1998) (2)
- Syntheses and Rearrangements of Spirocyclic Oxaziridines Derived from Unsymmetrical Ketones. (1991) (1)
- Synthetic Aspects of an Asymmetric Nitrogen-Insertion Process: Preparation of Chiral, Non-Racemic Caprolactams and Valerolactams. Total Synthesis of (-)-Alloyohimbane. (1990) (0)
- Protease inhibitors useful for the treatment of HIV AIDS. (1993) (0)
- Directed Regiochemical Control in Ring Expansion Reactions of a Substituted trans-Decalone. (1991) (0)
- Enantioselective Synthesis of Neocarzinostatin Chromophore Aglycon ( VII). (1997) (0)
- A Concise Synthesis of the Naphthoic Acid Component of Neocarzinostatin Chromophore Featuring a New Photocyclization Reaction. (1996) (0)
- Erratum: Syntheses and rearrangements of spirocyclic oxaziridines derived from unsymmetrical ketones (Journal of Organic Chemistry (1991) 56, (502)) (1991) (0)
- Graphical contents list (2009) (0)
- Directed regiochemicalcontrolin thering expansion reactionsofasubstituted trans-decalone (1992) (0)
- A Mild, Osmium Tetraoxide‐Catalyzed Method in the Oxidation of Sulfides to Sulfones. (1992) (0)
- Cannabino¤dreceptorliganden and uses thereof. (2004) (0)
- Spiro [isobenzofuran-1,4'-piperidin] -3-one and 3-hour spiroisobenzofuran-1,4'-piperidine (2001) (0)
- HIV protease inhibitors, useful for the treatment of AIDS (1993) (0)
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