6,7,8,10-Tetra-O-benzyl-1,2,3,4-tetradeoxy-α-D-gluco-dec-5-ulopyranosyl 2,3,4,6-Tetra-O-benzyl-α-D-glucopyranoside

doi:10.3390/M671

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Molbank 2010, 2010(2), M671; doi:10.3390/M671

Short Note

6,7,8,10-Tetra-O-benzyl-1,2,3,4-tetradeoxy-α-D-gluco-dec-5-ulopyranosyl 2,3,4,6-Tetra-O-benzyl-α-D-glucopyranoside

Takashi Yamanoi^1,* , Ryo Inoue^1,2, Yoshiki Oda¹ and Keita Hamasaki²

¹ The Noguchi Institute, 1-8-1 Kaga, Itabashi-ku, Tokyo 173-0003, Japan ² Department of Applied Chemistry, Shibaura Institute of Technology, 3-7-5 Toyosu, Koto-ku, Tokyo 135-8548, Japan

* Author to whom correspondence should be addressed.

Received: 17 March 2010 / Accepted: 1 April 2010 / Published: 7 April 2010

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Abstract: The title compound 1 was synthesized by the coupling reaction of 6,7,8,10-tetra-O-benzyl-1,2,3,4-tetradeoxy-α-D-gluco-dec-5-ulopyranose (2) with 2,3,4,6-tetra-O-benzyl-D-glucopyranose (3) in the presence of 5 mol% bismuth(III) triflate in dichloromethane at 0 °C.

Keywords: trehalose mimic; ketose; glucose; bismuth triflate

Supplementary Files

Supplementary File 1:
M671 3D structure (MOL, 8 KB) Display in MOL Viewer
3D structure generated by CORINA by Molecular Networks.
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Cite This Article

MDPI and ACS Style

Yamanoi, T.; Inoue, R.; Oda, Y.; Hamasaki, K. 6,7,8,10-Tetra-O-benzyl-1,2,3,4-tetradeoxy-α-D-gluco-dec-5-ulopyranosyl 2,3,4,6-Tetra-O-benzyl-α-D-glucopyranoside. Molbank 2010, 2010, M671.

AMA Style

Yamanoi T, Inoue R, Oda Y, Hamasaki K. 6,7,8,10-Tetra-O-benzyl-1,2,3,4-tetradeoxy-α-D-gluco-dec-5-ulopyranosyl 2,3,4,6-Tetra-O-benzyl-α-D-glucopyranoside. Molbank. 2010; 2010(2):M671.

Chicago/Turabian Style

Yamanoi, Takashi; Inoue, Ryo; Oda, Yoshiki; Hamasaki, Keita. 2010. "6,7,8,10-Tetra-O-benzyl-1,2,3,4-tetradeoxy-α-D-gluco-dec-5-ulopyranosyl 2,3,4,6-Tetra-O-benzyl-α-D-glucopyranoside." Molbank 2010, no. 2: M671.

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