266693-87-2Relevant academic research and scientific papers
A new convergent route to aldohexoses from a common chiral building block.
Honzumi,Taniguchi,Ogasawara
, p. 1355 - 1358 (2007/10/03)
[reaction in text] A diastereocontrolled route to the eight aldohexoses has been developed starting from a common cyclohexanoid chiral building block.
Integrated synthesis of conduritols A-F using a single chiral building block
Honzumi, Masatoshi,Hiroya, Kou,Taniguchi, Takahiko,Ogasawara, Kunio
, p. 1985 - 1986 (2007/10/03)
Six possible diastereomers of conduritols have been synthesized diastereoselectively in an integrated manner starting from a single chiral precursor, which served as a synthetic equivalent of chiral cis-1,4-dihydroxycyclohexa-2,5-diene.
