5398-65-2Relevant articles and documents
Enantiomerically pure 2,2-dibromocyclopropanecarboxylic acids, simple chiral building blocks
Baird, Mark S.,Licence, Peter,Tverezovsky, Viacheslav V.,Bolesov, Ivan G.,Clegg, William
, p. 2773 - 2784 (1999)
Simple chiral building blocks 1-(R)- and 1-(S)-2,2- dibromocyclopropanecarboxylic acids and 2-(R)-bromo-1-(S')- cyclopropanecarboxylic acids and their 1-methyl analogues, have been obtained on a preparatively useful laboratory scale.
Thermodynamic control of diastereoselectivity in the formal nucleophilic substitution of bromocyclopropanes
Banning, Joseph E.,Prosser, Anthony R.,Rubin, Michael
supporting information; experimental part, p. 1488 - 1491 (2010/06/21)
(Figure Presented) A new, general, and chemoselective protocol for the formal nucleophilic substitution of 2-bromocyclopropylcarboxamides is described. A wide range of alcohols and phenols can be employed as pronucleophiles in this transformation, providi
Synthese von funktionalisierten bi(cyclopropylidenen)
Huwyler, Rolf,Al-Dulayymi, Ahmad,Neuenschwander, Markus
, p. 2336 - 2347 (2007/10/03)
In view of the synthesis of attractive triafulvalene precursors 9, a series of bi(cyclopropylidenes) 8 with vinyl(8a), alkoxycarbonyl (8c-f), hydroxymethyl (8h), as well as protected hydroxymethyl groups (8g, 8i) have been prepared by simple one-pot react