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Regioselective reduction of 4,6-O-benzylidenes using triethylsilane and BF3.Et2O

Publication ,  Journal Article
Debenham, SD; Toone, EJ
Published in: Tetrahedron Asymmetry
February 11, 2000

The 4,6-di-O-benzylidene acetals of glucose, mannose, glucosamine, and galactose were regioselectively reduced by triethylsilane in the presence of BF3.Et2O to yield the 6-O-benzyl ethers in good to excellent yields. Copyright (C) 2000 Elsevier Science Ltd.

Duke Scholars

Published In

Tetrahedron Asymmetry

DOI

ISSN

0957-4166

Publication Date

February 11, 2000

Volume

11

Issue

2

Start / End Page

385 / 387

Related Subject Headings

  • Organic Chemistry
  • 3405 Organic chemistry
  • 0305 Organic Chemistry
 

Citation

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Debenham, S. D., & Toone, E. J. (2000). Regioselective reduction of 4,6-O-benzylidenes using triethylsilane and BF3.Et2O. Tetrahedron Asymmetry, 11(2), 385–387. https://doi.org/10.1016/S0957-4166(99)00584-4
Debenham, S. D., and E. J. Toone. “Regioselective reduction of 4,6-O-benzylidenes using triethylsilane and BF3.Et2O.” Tetrahedron Asymmetry 11, no. 2 (February 11, 2000): 385–87. https://doi.org/10.1016/S0957-4166(99)00584-4.
Debenham SD, Toone EJ. Regioselective reduction of 4,6-O-benzylidenes using triethylsilane and BF3.Et2O. Tetrahedron Asymmetry. 2000 Feb 11;11(2):385–7.
Debenham, S. D., and E. J. Toone. “Regioselective reduction of 4,6-O-benzylidenes using triethylsilane and BF3.Et2O.” Tetrahedron Asymmetry, vol. 11, no. 2, Feb. 2000, pp. 385–87. Scopus, doi:10.1016/S0957-4166(99)00584-4.
Debenham SD, Toone EJ. Regioselective reduction of 4,6-O-benzylidenes using triethylsilane and BF3.Et2O. Tetrahedron Asymmetry. 2000 Feb 11;11(2):385–387.
Journal cover image

Published In

Tetrahedron Asymmetry

DOI

ISSN

0957-4166

Publication Date

February 11, 2000

Volume

11

Issue

2

Start / End Page

385 / 387

Related Subject Headings

  • Organic Chemistry
  • 3405 Organic chemistry
  • 0305 Organic Chemistry