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Chemical Communications (Cambridge, England)|July 12, 2002
Sex pheromone biosynthesis in the female olive fruit-fly. Double labelling from [18O2]-dioxygen into 1,7-dioxaspiro[5.5]undecaneMary T Fletcher, Basilis E Mazomenos, John H Georgakopoulos, et al.Organic Letters|December 20, 2003
4,6,8,10,16-penta- and 4,6,8,10,16,18-hexamethyldocosanes from the cane beetle antitrogusparvulus--cuticular hydrocarbons with unprecedented structure and stereochemistryMary T Fletcher, Sharon Chow, Lynette K Lambert, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|May 21, 2011
The truth about false unicorn (Chamaelirium luteum): total synthesis of 23R,24S-chiograsterol B defines the structure and stereochemistry of the major saponins from this medicinal herbNicholas J Matovic, Julia M U Stuthe, Victoria L Challinor, et al.The Journal of Organic Chemistry|February 26, 2005
Novel cuticular hydrocarbons from the cane beetle Antitrogus parvulus--4,6,8,10,16-penta- and 4,6,8,10,16,18-hexamethyldocosanes-unprecedented anti-anti-anti-stereochemistry in the 4,6,8,10-methyltetradSharon Chow, Mary T Fletcher, Lynette K Lambert, et al.Organic Letters|March 12, 2005
Spiroacetal biosynthesis: (+/-)-1,7-dioxaspiro[5.5]undecane in Bactrocera cacuminata and Bactrocera oleae (Olive Fruit Fly)Brett D Schwartz, Christopher S P McErlean, Mary T Fletcher, et al.Journal of Natural Products|August 14, 2012
Structure and bioactivity of steroidal saponins isolated from the roots of Chamaelirium luteum (false unicorn)Victoria L Challinor, Julia M U Stuthe, Peter G Parsons, et al.Chirality|July 29, 2003
Insect chemistry and chiralityPatricia Y Hayes, Mary T Fletcher, Sharon Chow, et al.Pageof 3