93132-83-3Relevant articles and documents
USING THE COMPARISON OF STERIC VERSUS ELECTRONIC EFFECTS TO INFER MECHANISTIC INFORMATION IN STEPWISE ELECTROPHILIC ADDITION REACTIONS INVOLVING THREE-MEMBERED CYCLIC INTERMEDIATES
Nelson, Donna J.,Soundararajan, Raman
, p. 6207 - 6210 (1988)
Correlations of IP's versus relative reactivities or formation constants of reactions of alkenes with ArSCl, MeCO3H, Ag(1+), or HgCl2 reveal that complexation reactions show steric dependence, that additions with the first step rate-determining are sterically independent, and that those with the second step rate-determining are sterically dependent.
(4 S,5 S)-2,2,4-Triethyl-5-methyl-1,3-dioxolane: A new volatile released by a triatomine bug
Unelius,Bohman,Lorenzo,Troeger,Franke,Francke
supporting information; experimental part, p. 5601 - 5603 (2011/03/20)
Adults of the triatomine bug Triatoma brasiliensis release 2,2,4-triethyl-5-methyl-1,3-dioxolane (1) as a mixture of the (4S,5S)- and (4R,5R)-enantiomers in a ratio of 4:1. Among the volatile acetals identified from insects so far, this is the first example resulting from an intermolecular condensation of a carbonyl moiety and a diol substructure.