Preparation of chiral cyclopropanecarboxylic acids and 3-oxabicyclo[3.1.0]hexane-2-ones from levoglucosenone Full article
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Tetrahedron: Asymmetry
ISSN: 1362-511X , E-ISSN: 0957-4166 |
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| Output data | Year: 2008, Volume: 19, Number: 6, Pages: 691-694 Pages count : 4 DOI: 10.1016/j.tetasy.2008.02.016 | ||
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Abstract:
Levoglucosenone (a chiral α,β-unsaturated ketone derivative of cellulose) serves as a starting compound in 2 and 3 step syntheses of chiral cyclopropanecarboxylic acids and 3-oxabicyclo[3.1.0]hexane-2-ones, respectively.
Cite:
Samet A.V.
, Lutov D.N.
, Konyushkin L.D.
, Strelenko Y.A.
, Semenov V.V.
Preparation of chiral cyclopropanecarboxylic acids and 3-oxabicyclo[3.1.0]hexane-2-ones from levoglucosenone
Tetrahedron: Asymmetry. 2008. V.19. N6. P.691-694. DOI: 10.1016/j.tetasy.2008.02.016 OpenAlex
Preparation of chiral cyclopropanecarboxylic acids and 3-oxabicyclo[3.1.0]hexane-2-ones from levoglucosenone
Tetrahedron: Asymmetry. 2008. V.19. N6. P.691-694. DOI: 10.1016/j.tetasy.2008.02.016 OpenAlex
Identifiers:
| ≡ OpenAlex: | W2007813488 |