208035-47-6Relevant academic research and scientific papers
An expeditious route to the synthesis of highly functionalized chiral oxepines from monosaccharides
Ovaa, Huib,Leeuwenburgh, Michiel A.,Overkleeft, Herman S.,Van Der Marel, Gijs A.,Van Boom, Jacques H.
, p. 3025 - 3028 (1998)
The transformation of partially protected aldofuranoses into dienes by Wittig olefination of the anomeric center followed by either allylation or oxopalladation of alkoxy-1,2-propadienes is described. Ring-closing metastasis of the linear dienes gives rise to a variety of highly functionalized and chiral ring-expanded oxepines.
Tandem RCM-isomerization approach to glycals of desoxyheptoses from a common precursor
Schmidt, Bernd,Biernat, Anne
, p. 105 - 108 (2008/04/12)
Ring closing metathesis and tandem RCM-isomerization have been applied to the synthesis of six- to eight-membered oxacycles, starting from a common precursor. The products of the tandem RCM-isomerization sequence are glycals of 3-deoxyheptoses of varying
