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Peter Wipf

Researcher at University of Pittsburgh

Publications -  795
Citations -  27717

Peter Wipf is an academic researcher from University of Pittsburgh. The author has contributed to research in topics: Total synthesis & Transmetalation. The author has an hindex of 83, co-authored 767 publications receiving 25316 citations. Previous affiliations of Peter Wipf include University of California, Los Angeles & University of Vermont.

Papers
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Journal ArticleDOI

Transient Delivery of a KCNQ2/3-Specific Channel Activator 1 Week After Noise Trauma Mitigates Noise-Induced Tinnitus

TL;DR: In this paper, a very potent and highly specific activator of Kv7.2/3 channels was developed for noise-induced tinnitus in mice and tested in an operant animal model, where mice are trained to move in response to sound but not move in silence.
Patent

Use of targeted nitroxide agents in bone healing

TL;DR: In this article, compositions and related methods useful for accelerating bone healing and growth are presented and cross-linked into dimers without loss of activity, where the compounds comprise a nitroxide-containing group attached to a mitochondria-targeting group.
Patent

Small molecule inhibitors of the nuclear translocation of androgen receptor for the treatment of castration-resistant prostate cancer

TL;DR: A compound, or a pharmaceutically acceptable salt or ester thereof, according to formula I: R 20 is H or alkyl; R 22 includes at least one divalent amino radical; R 23 is aryl, substituted aryyl, heteroaryl, substituted hetero-aryl, cycloalkyl, substituted cyclo-alkycloalky, heterocyclo-labeled, cycloencyl, substituting cyclohexanecyclo-cycloalkynediyl, and substituted cycloencyclohex
Journal ArticleDOI

Dimethylzinc-Mediated Additions of Alkenylzirconocenes to Aldimines. New Methodologies for Allylic Amine and C-Cyclopropylalkylamine Syntheses.

TL;DR: In this article, a transition state that explains the need for both zirconocene complex and alkyl zinc in the cyclopropanation reaction is proposed, which allows the stereoselective formation of five new carbon-carbon bonds.