Reaction:JCGG-RAC0001310

JCGG ID		JCGG-RAC0001310
Submitter		The Noguchi Institute
Reaction ID		R-0000-001310
Regist Date		2012/06/21 16:50:05
REACTANT
MOLECULE ID		JCGG-COM0001478 (Reaction Tree)
	Mol	6.96 mmol
MOLECULE ID		JCGG-COM0000160
	Reactant Type	NaH
	Mol	14.9 micro mol
MOLECULE ID		JCGG-COM0000831
	Reactant Type	PMBCl
	Mol	37.1 mmol
PRODUCT
MOLECULE ID		JCGG-COM0001451 (Reaction Tree)
	Yield	91%
REACTION DETAIL
Reaction Time		2 hours
Reaction Temp		0 degree C
Solvent		dry DMF
COMMENT
Keywords: stereoselective synthesis, mycobacterial arabinan, arabinofuranosyl donors, arabinofuranosylation, TIDPS
REFERENCE
Reference Id		REF-0000-000067
	Issn	Print
	Doi	10.1021/ol062198j
	PubMed ID	17107063
	Journal Name	Organic letters. (2006) 8 (24): 5525-8.
	Article Title	Stereoselective synthesis of a fragment of mycobacterial arabinan.
	Author	Akihiro, Ishiwata; Hiroko, Akao; Yukishige, Ito
	Affiliation	RIKEN (Institute of Physical and Chemical Research), Wako-shi, Saitama 351-0198, Japan.
Reference Id		REF-0000-000068
	Source	ORGANIC LETTERS, 2006, Vol. 8, No. 24, 5525-5528
	Doi	10.1021/ol062198j