1613145-23-5Relevant articles and documents
Diastereo- and enantioselective synthesis of 1,3,5,7-tetraol structural units using a Prins cyclisation-reductive cleavage sequence
Brun, Elodie,Bellosta, Véronique,Cossy, Janine
supporting information, p. 6718 - 6721 (2014/06/23)
Stereocontrolled and efficient access to all the diastereomers of 1,3,5,7-tetraol structural units was developed using a Prins cyclisation-reductive cleavage sequence applied to tetrahydropyran aldehydes. Furthermore, these tetraols can be selectively functionalized. This journal is the Partner Organisations 2014.