4462-97-9Relevant academic research and scientific papers
SYNTHESIS OF NEW CARBOCYCLIC ANALOGUES OF OXETANOCIN A AND OXETANOCIN G
Pecquet, Pascal,Huet, Francois,Legraverend, Michel,Bisagni, Emile
, p. 739 - 745 (2007/10/02)
The synthesis of cis-3-amino-1-cyclobutanemethanol has been performed in six steps (59.6percent yield) from cis-1,3-cyclobutanedicarboxylic anhydride.This allowed us to obtain two new carbocyclic analogues of oxetanocin A and oxetanocin G related to 7-deazaadenosine and 7-deazaguanosine.
On the Reduction of Benzvalene Ozonide to cis-1,3-Cyclobutanedimethanol with LiAlH4
Leininger, Hartmut,Lanzendoerfer, Franz,Christl, Manfred
, p. 669 - 680 (2007/10/02)
On treatment with LiAlH4 at -30 deg C the polymeric ozonide of benzvalene (1) gives bicyclobutane-endo,endo-2,4-dimethanol (7).At higher temperatures cis-1,3-cyclobutanedimethanol (4) is formed.The stereochemical course of this unusual C-C hydrogenolysis has been elucidated by means of deuterated substrates.For this purpose a complete analysis of 1H NMR spectra of the labeled cis-1,3-cyclobutanedicarboxylic anhydrides 9a-c had to be carried out.The dialcohol 7 and its bismethyl ether 16 add thiophenol across the central bond to form the cis products 18 and 19, respectively.Acids or Ag+ ions isomerize 7 via cleavage of a lateral bond into the ethers 21.
