Reaction:JCGG-RAC0000207

JCGG ID		JCGG-RAC0000207
Submitter		The Noguchi Institute
Reaction ID		R-0000-000207
Regist Date		2012/06/21 14:52:45
REACTANT
MOLECULE ID		JCGG-COM0000226 (Reaction Tree)
	Reactant Type	Donor[1,3,4,6-tetra-O-benzyl-D-frucofuranosyl acetate (alpha/beta=1/2)]
	Mol	1
MOLECULE ID		JCGG-COM0000006
	Reactant Type	Activator
	Mol	0.05
MOLECULE ID		JCGG-COM0000037
	Reactant Type	Acceptor
	Mol	1
PRODUCT
MOLECULE ID		JCGG-COM0000239 (Reaction Tree)
	Product Type	alpha
	Yield	92%(alpha/beta=65/35)
MOLECULE ID		JCGG-COM0000240 (Reaction Tree)
	Product Type	beta
	Yield	92%(alpha/beta=65/35)
REACTION DETAIL
Reaction Time		0.5 hour to overnight
Reaction Temp		0 degree C
Solvent		PhCH3
Catalyst		Activator
Comment		Anhydrous CaSO4 was included in the solvent.
COMMENT
The PMID could not be found.
REFERENCE
Reference Id		REF-0000-000011
	Source	Tetrahedron Letters 48 (2007) 6458‐6462
	Doi	10.1016/j.tetlet.2007.07.092