855306-33-1Relevant articles and documents
Convergent synthesis of a β-(1→3)-mannohexaose
Crich, David,Wu, Baolin,Jayalath, Prasanna
, p. 6806 - 6815 (2008/02/12)
(Chemical Equation Presented) An as yet unknown β-(1→3)- mannohexaose has been synthesized by a block route involving the coupling of two trisaccharides. Comparison of three closely related attempted mannohexaose syntheses reinforces the influence of subt
2-O-Propargyl ethers: Readily cleavable, minimally intrusive protecting groups for β-mannosyl donors
Crich, David,Jayalath, Prasanna
, p. 2277 - 2280 (2007/10/03)
(Chemical Equation Presented) The use of 2-O-propargyl ethers as protecting groups in 4,6-O-benzylidene-protected mannopyranosyl donors bearing either bulky silyl groups or glycosidic linkages on O3 overcomes the poor stereoselectivity achieved with the c