Todd R. Ryder, Ph.D.

Affiliations: 
2006 University of Rochester, Rochester, NY 
Area:
Synthetic Organic Chemistry
Google:
"Todd Ryder"
Mean distance: 8.32
 
SNBCP

Parents

Sign in to add mentor
Robert K. Boeckman, Jr. grad student 2006 Rochester
 (1. Synthesis of a (+)-discodermolide analog. 2. Studies of (-)-nakadomarin A.)
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Boeckman RK, Wang H, Rugg KW, et al. (2016) A Scalable Total Synthesis of (-)-Nakadomarin A. Organic Letters. 18: 6136-6139
Golebiowski A, Whitehouse D, Beckett RP, et al. (2013) Synthesis of quaternary α-amino acid-based arginase inhibitors via the Ugi reaction. Bioorganic & Medicinal Chemistry Letters. 23: 4837-41
Van Zandt MC, Whitehouse DL, Golebiowski A, et al. (2013) Discovery of (R)-2-amino-6-borono-2-(2-(piperidin-1-yl)ethyl)hexanoic acid and congeners as highly potent inhibitors of human arginases I and II for treatment of myocardial reperfusion injury. Journal of Medicinal Chemistry. 56: 2568-80
Golebiowski A, Paul Beckett R, Van Zandt M, et al. (2013) 2-Substituted-2-amino-6-boronohexanoic acids as arginase inhibitors. Bioorganic & Medicinal Chemistry Letters. 23: 2027-30
Boeckman RK, Miller Y, Ryder TR. (2010) Diels-Alder reactions of cyclic isoimidium salts. Organic Letters. 12: 4524-7
Boeckman RK, Genung NE, Chen K, et al. (2010) Synthetic and mechanistic studies of the aza-retro-Claisen rearrangement. A facile route to medium ring nitrogen heterocycles. Organic Letters. 12: 1628-31
Hu LY, Boxer PA, Kesten SR, et al. (2006) The design and synthesis of human branched-chain amino acid aminotransferase inhibitors for treatment of neurodegenerative diseases. Bioorganic & Medicinal Chemistry Letters. 16: 2337-40
Hu LY, Ryder TR, Rafferty MF, et al. (2000) Neuronal N-type calcium channel blockers: a series of 4-piperidinylaniline analogs with analgesic activity. Drug Design and Discovery. 17: 85-93
Hu LY, Ryder TR, Rafferty MF, et al. (2000) The discovery of [1-(4-dimethylamino-benzyl)-piperidin-4-yl]-[4-(3,3-dimethylbutyl)-phen yl]-(3-methyl-but-2-enyl)-amine, an N-type Ca+2 channel blocker with oral activity for analgesia. Bioorganic & Medicinal Chemistry. 8: 1203-12
Ryder TR, Hu LY, Rafferty MF, et al. (2000) Structure-activity relationship at the leucine side chain in a series of N,N-dialkyldipeptidyl-amines as N-type calcium channel blockers. Drug Design and Discovery. 16: 317-22
See more...