119649-45-5Relevant articles and documents
The di-t-butylsilylene protecting group as a bridging unit in linear and macrocyclic bis-malonates for the regioselective multifunctionalization of C60
Guerra, Sebastiano,Trinh, Thi Minh Nguyet,Schillinger, Franck,Muhlberger, Lucie,Sigwalt, David,Holler, Michel,Nierengarten, Jean-Fran?ois
, p. 6251 - 6257 (2013)
Fullerene equatorial bis-adducts have been prepared with high regioselectivity by a double Bingel reaction between [60]fullerene and di-t-butylsilylene-tethered bis-malonates. Macrocyclic bis-malonates incorporating di-t-butylsilylene moieties have also b
Regioselective Preparation of Fullerene Bis-adducts from Cleavable Macrocyclic Bis-malonates
Trinh, Thi Minh Nguyet,Schillinger, Franck,Guerra, Sebastiano,Meichsner, Eric,Nierengarten, Iwona,Hahn, Uwe,Holler, Michel,Nierengarten, Jean-Fran?ois
, p. 3770 - 3786 (2021/06/27)
A series of macrocyclic bis-malonates incorporating either di-tert-butylsilylene or tetra-iso-propyldisiloxane subunits have been prepared and used for the regioselective bis-functionalization of [60]fullerene by double Bingel cyclopropanations. By system
Fluorine in pheromones: Synthesis of fluorinated 12-dodecanolides as emerald ash borer pheromone mimetics
Zhang, Qingzhi,Teschers, Charlotte S.,Callejo, Ricardo,Yang, Mingyan,Wang, Mingan,Silk, Peter J.,Ryall, Krista,Roscoe, Lucas E.,Cordes, David B.,Slawin, Alexandra M.Z.,O'Hagan, David
supporting information, p. 2917 - 2922 (2019/04/30)
A series of five 12-dodecanolides have been synthesised containing CF2 groups at C5, C6, C7, C8 and in one case, a double substitution at C5 & C8, as a strategy to bias the conformational space accessed by these macrocycles, and to assess if th