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Journal of the American Chemical Society|January 23, 2016
Unprecedented Intramolecular [4 + 2]-Cycloaddition between a 1,3-Diene and a Diazo EsterHuang Qiu, Harathi D Srinivas, Peter Y Zavalij, et al.
Dalton Transactions (Cambridge, England : 2003)|January 8, 2015
Synthesis, structure, and properties of a dialumane supported by pyrazolate ligandsChristopher J Snyder, Peter Zavalij, Kit Bowen, et al.
Organic Letters|July 1, 2015
Lewis Acid/Rhodium-Catalyzed Formal [3 + 3]-Cycloaddition of Enoldiazoacetates with Donor-Acceptor CyclopropanesQing-Qing Cheng, Yu Qian, Peter Y Zavalij, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|July 14, 2020
Acyclic Cucurbit[n]uril-Type Receptors: Aromatic Wall Extension Enhances Binding Affinity, Delivers Helical Chirality, and Enables Fluorescence SensingSteven Murkli, Jared Klemm, David King, et al.
Acta Crystallographica. Section E, Crystallographic Communications|March 24, 2016
Crystal and mol-ecular structure of meso-2,6-di-bromo-hepta-nedioic acid (meso-2,6-di-bromo-pimelic acid)Nathaniel D A Dirda, Peter Y Zavalij, Joseph P Y Kao
The Journal of Organic Chemistry|March 30, 2010
Reasons why aldehydes do not generally participate in cucurbit[n]uril forming reactionsDa Ma, Zuzana Gargulakova, Peter Y Zavalij, et al.
Organic & Biomolecular Chemistry|March 4, 2015
Acyclic cucurbit[n]uril-type molecular containers: influence of glycoluril oligomer length on their function as solubilizing agentsLaura Gilberg, Ben Zhang, Peter Y Zavalij, et al.
Angewandte Chemie (International Ed. in English)|April 25, 2024
Acyclic Cucurbit[n]uril Receptors Function as Solid State Sequestrants for Organic MicropollutantsSuvenika Perera, Alok Shaurya, Michael Baptiste, et al.
The Journal of Organic Chemistry|July 1, 2008
Self-sorting molecular clipsSoumyadip Ghosh, Anxin Wu, James C Fettinger, et al.
Journal of the American Chemical Society|September 28, 2010
Preparation and C-X reductive elimination reactivity of monoaryl Pd(IV)-X complexes in water (X = OH, OH2, Cl, Br)Williamson Oloo, Peter Y Zavalij, Jing Zhang, et al.
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