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Journal of the American Chemical Society|June 3, 2015
A synthesis of alsmaphorazine B demonstrates the chemical feasibility of a new biogenetic hypothesisAllen Y Hong, Christopher D VanderwalSynthesis|September 25, 2025
A Chlorine-Bearing Asymmetric Center as a Stereocontrol Element in a Short Formal Synthesis of SteviolSharon E Michalak, Christopher D VanderwalAngewandte Chemie (International Ed. in English)|February 3, 2016
Stereoselective Halogenation in Natural Product SynthesisWon-jin Chung, Christopher D VanderwalJournal of the American Chemical Society|May 20, 2009
Complex polycyclic lactams from pericyclic cascade reactions of Zincke aldehydesSarah E Steinhardt, Christopher D VanderwalOrganic Letters|August 9, 2014
Investigations into an anionic oxy-cope/transannular conjugate addition approach to 7,20-diisocyanoadocianePhilipp C Roosen, Christopher D VanderwalNatural Product Reports|December 3, 2010
Chlorosulfolipids: structure, synthesis, and biological relevanceD Karl Bedke, Christopher D VanderwalThe Journal of Organic Chemistry|September 15, 2010
Ring-closing metathesis of allylsilanes as a flexible strategy toward cyclic terpenes. short syntheses of teucladiol, isoteucladiol, poitediol, and dactylol and an attempted synthesis of caryophylleneMatthew S Dowling, Christopher D VanderwalEuropean Journal of Organic Chemistry|March 13, 2018
Strategies for the Synthesis of the Halenaquinol and Xestoquinol Families of Natural ProductsGregg M Schwarzwalder, Christopher D VanderwalJournal of the American Chemical Society|November 13, 2004
Enantioselective formal hydration of alpha,beta-unsaturated imides by Al-catalyzed conjugate addition of oxime nucleophilesChristopher D Vanderwal, Eric N JacobsenJournal of the American Chemical Society|October 1, 2009
Ring-closing metathesis of allylsilanes/electrophilic desilylation to prepare exo-methylidenecycloalkanes. Short syntheses of teucladiol and poitediolMatthew S Dowling, Christopher D VanderwalPageof 11