140386-94-3Relevant articles and documents
Synthesis of optically active monothioimides with chirality due to sulphur substitution
Milewska,Polonski
, p. 359 - 362 (1994)
Two optically active bicyclic monothioimides were prepared via chiral derivatives of cis-1,2-cyclopropanedicarboxylic and cis-1,3-cyclopentanedicarboxylic acids and their absolute configurations were assigned.
Synthesis and antiviral activities of some novel carbocyclic nucleosides
Carmen Balo,Fernandez, Franco,Lens, Evangelina,Lopez, Carmen,De Clercq, Erik,Andrei, Graciela,Snoeck, Robert,Baizarini, Jan
, p. 1335 - 1346 (2007/10/03)
cis-3-Aminomethylcyclopentylmethanol (4), prepared from norbornene (5) in four steps and 51% overall yield, was used as a precursor in the synthesis of carbocylic nucleosides 13 - 18 containing guanine and 8-azaguanine bases. None of these compounds had a
Enantioselective synthesis of (+) and (-)-cis-3-aminocyclopentanecarboxylic acids by enzymatic asymmetrization
Chenevert,Martin
, p. 199 - 200 (2007/10/02)
Both enantiomers of cis-3-aminocyclopentanecarboxylic acid (GABA analogs, inhibitory neurotransmitter) have been prepared via enzymatic asymmetrization of cis -1,3-cyclopentanedicarboxylic acid.
