Regioselective reduction of 4,6-O-benzylidenes using triethylsilane and BF3 .Et2 O
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
APA
Chicago
ICMJE
MLA
NLM
Debenham, S. D., & Toone, E. J. (2000). Regioselective reduction of 4,6-O-benzylidenes using triethylsilane and BF3 .Et2 O. 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 .Et2 O.” 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 .Et2 O. 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 .Et2 O.” 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 .Et2 O. Tetrahedron Asymmetry. 2000 Feb 11;11(2):385–387.
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