Enantioselective synthesis and selective monofunctionalization of (4R,6R)-4,6-dihydroxy-2,8-dioxabicyclo[3.3.0]octane
- Author
- Bruno Linclau (UGent) , Martin J. Jeffery, Solen Josse and Cyrille Tomassi
- Organization
- Abstract
- An efficient, enantioselective synthesis of a disubstituted bis-THF scaffold 5 is described, as well as an efficient differentiation of the 1,3-diol unit.
- Keywords
- HIV PROTEASE INHIBITORS, STEREOCONTROLLED SYNTHESIS, ASPERGILLUS-STELLATUS, FURO<2, 3B>FURANS, METATHESIS, MYCOTOXIN, ARABITOL
Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-01GMMXB1R7KJB5ACVJKSFDRE0F
- MLA
- Linclau, Bruno, et al. “Enantioselective Synthesis and Selective Monofunctionalization of (4R,6R)-4,6-Dihydroxy-2,8-Dioxabicyclo[3.3.0]Octane.” ORGANIC LETTERS, vol. 8, no. 25, 2006, pp. 5821–24, doi:10.1021/ol062431d.
- APA
- Linclau, B., Jeffery, M. J., Josse, S., & Tomassi, C. (2006). Enantioselective synthesis and selective monofunctionalization of (4R,6R)-4,6-dihydroxy-2,8-dioxabicyclo[3.3.0]octane. ORGANIC LETTERS, 8(25), 5821–5824. https://doi.org/10.1021/ol062431d
- Chicago author-date
- Linclau, Bruno, Martin J. Jeffery, Solen Josse, and Cyrille Tomassi. 2006. “Enantioselective Synthesis and Selective Monofunctionalization of (4R,6R)-4,6-Dihydroxy-2,8-Dioxabicyclo[3.3.0]Octane.” ORGANIC LETTERS 8 (25): 5821–24. https://doi.org/10.1021/ol062431d.
- Chicago author-date (all authors)
- Linclau, Bruno, Martin J. Jeffery, Solen Josse, and Cyrille Tomassi. 2006. “Enantioselective Synthesis and Selective Monofunctionalization of (4R,6R)-4,6-Dihydroxy-2,8-Dioxabicyclo[3.3.0]Octane.” ORGANIC LETTERS 8 (25): 5821–5824. doi:10.1021/ol062431d.
- Vancouver
- 1.Linclau B, Jeffery MJ, Josse S, Tomassi C. Enantioselective synthesis and selective monofunctionalization of (4R,6R)-4,6-dihydroxy-2,8-dioxabicyclo[3.3.0]octane. ORGANIC LETTERS. 2006;8(25):5821–4.
- IEEE
- [1]B. Linclau, M. J. Jeffery, S. Josse, and C. Tomassi, “Enantioselective synthesis and selective monofunctionalization of (4R,6R)-4,6-dihydroxy-2,8-dioxabicyclo[3.3.0]octane,” ORGANIC LETTERS, vol. 8, no. 25, pp. 5821–5824, 2006.
@article{01GMMXB1R7KJB5ACVJKSFDRE0F,
abstract = {{An efficient, enantioselective synthesis of a disubstituted bis-THF scaffold 5 is described, as well as an efficient differentiation of the 1,3-diol unit.}},
author = {{Linclau, Bruno and Jeffery, Martin J. and Josse, Solen and Tomassi, Cyrille}},
issn = {{1523-7060}},
journal = {{ORGANIC LETTERS}},
keywords = {{HIV PROTEASE INHIBITORS,STEREOCONTROLLED SYNTHESIS,ASPERGILLUS-STELLATUS,FURO<2,3B>FURANS,METATHESIS,MYCOTOXIN,ARABITOL}},
language = {{eng}},
number = {{25}},
pages = {{5821--5824}},
title = {{Enantioselective synthesis and selective monofunctionalization of (4R,6R)-4,6-dihydroxy-2,8-dioxabicyclo[3.3.0]octane}},
url = {{http://doi.org/10.1021/ol062431d}},
volume = {{8}},
year = {{2006}},
}
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