a public good project by the
Synthesis
Company
of California

© 2026

Andrew S. Kende | doi.page

0 works0 citations0 h-index

Andrew S. Kende

Publications by Year

Research Areas

Synthetic Organic Chemistry Methods, Oxidative Organic Chemistry Reactions, Asymmetric Synthesis and Catalysis, Fluorine in Organic Chemistry, Chemical synthesis and alkaloids

Most-Cited Works

→ Stereospecific, high affinity binding of 2,3,7,8-tetrachlorodibenzo-p-dioxin by hepatic cytosol. Evidence that the binding species is receptor for induction of aryl hydrocarbon hydroxylase.(1976)1,364 cited
→ Quinolone signaling in the cell-to-cell communication system of Pseudomonas aeruginosa(1999)1,089 cited
→ STUDIES ON THE MECHANISM OF ACTION OF THE CHLORINATED DIBENZO‐p‐DIOXINS AND RELATED COMPOUNDS*(1979)335 cited
→ Functional analysis of the Pseudomonas aeruginosa autoinducer PAI(1996)159 cited
→ 3,4,3′,4′-Tetrachloro Azoxybenzene and Azobenzene: Potent Inducers of Aryl Hydrocarbon Hydroxylase(1976)143 cited
→ Analysis of structural requirements for ah receptor antagonist activity: Ellipticines, flavones, and related compounds(1996)142 cited

→ generation of a solvated zerovalent nickel reagent. Biaryl formation(1975)

141 cited

→ Photoaffinity labeling of the Ah receptor.(1986)135 cited

→ Stereochemistry of deconjugative alkylation of ester dienolates. Stereospecific total synthesis of the litsenolides(1982)129 cited

→ Flavone Antagonists Bind Competitively with 2,3,7,8-Tetrachlorodibenzo-p-Dioxin (TCDD) to the Aryl Hydrocarbon Receptor But Inhibit Nuclear Uptake and Transformation(1999)129 cited