Lead tetraacetate oxidation of saturated aliphatic alcohols-IV. The formation of six-membered cyclic ethers
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1965
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Metapodaci
Prikaz svih podataka o dokumentuApstrakt
The lead tetraacetate oxidation of saturated aliphatic alcohols, with structures which do not permit 1,5-cyclization, gave tetrahydropyran derivatives in yields not exceeding 16%. The formation of a small amount of the rearranged ether, 2-ethyl-2-methyltetrahydrofuran, from 4,4-dimethyl-1-pentanol indicates that the cyclization reaction proceeds via an intermediate with carbonium ion character.
Ključne reči:
lead tetraacetate / oxidation / six-membered cyclic ethers / saturated aliphatic alcoholsIzvor:
Tetrahedron, 1965, 21, 10, 2813-2821Izdavač:
- Elsevier
Finansiranje / projekti:
- The Research Fund of SR Serbia, Yugoslavia
DOI: 10.1016/S0040-4020(01)98366-8
ISSN: 0040-4020; 1464-5416
Scopus: 2-s2.0-0141825638
Institucija/grupa
IHTMTY - JOUR AU - Mihailović, Milhailo Lj. AU - Čeković, Živorad M. AU - Jeremić, Dragoslav PY - 1965 UR - https://cer.ihtm.bg.ac.rs/handle/123456789/4628 AB - The lead tetraacetate oxidation of saturated aliphatic alcohols, with structures which do not permit 1,5-cyclization, gave tetrahydropyran derivatives in yields not exceeding 16%. The formation of a small amount of the rearranged ether, 2-ethyl-2-methyltetrahydrofuran, from 4,4-dimethyl-1-pentanol indicates that the cyclization reaction proceeds via an intermediate with carbonium ion character. PB - Elsevier T2 - Tetrahedron T1 - Lead tetraacetate oxidation of saturated aliphatic alcohols-IV. The formation of six-membered cyclic ethers VL - 21 IS - 10 SP - 2813 EP - 2821 DO - 10.1016/S0040-4020(01)98366-8 ER -
@article{ author = "Mihailović, Milhailo Lj. and Čeković, Živorad M. and Jeremić, Dragoslav", year = "1965", abstract = "The lead tetraacetate oxidation of saturated aliphatic alcohols, with structures which do not permit 1,5-cyclization, gave tetrahydropyran derivatives in yields not exceeding 16%. The formation of a small amount of the rearranged ether, 2-ethyl-2-methyltetrahydrofuran, from 4,4-dimethyl-1-pentanol indicates that the cyclization reaction proceeds via an intermediate with carbonium ion character.", publisher = "Elsevier", journal = "Tetrahedron", title = "Lead tetraacetate oxidation of saturated aliphatic alcohols-IV. The formation of six-membered cyclic ethers", volume = "21", number = "10", pages = "2813-2821", doi = "10.1016/S0040-4020(01)98366-8" }
Mihailović, M. Lj., Čeković, Ž. M.,& Jeremić, D.. (1965). Lead tetraacetate oxidation of saturated aliphatic alcohols-IV. The formation of six-membered cyclic ethers. in Tetrahedron Elsevier., 21(10), 2813-2821. https://doi.org/10.1016/S0040-4020(01)98366-8
Mihailović ML, Čeković ŽM, Jeremić D. Lead tetraacetate oxidation of saturated aliphatic alcohols-IV. The formation of six-membered cyclic ethers. in Tetrahedron. 1965;21(10):2813-2821. doi:10.1016/S0040-4020(01)98366-8 .
Mihailović, Milhailo Lj., Čeković, Živorad M., Jeremić, Dragoslav, "Lead tetraacetate oxidation of saturated aliphatic alcohols-IV. The formation of six-membered cyclic ethers" in Tetrahedron, 21, no. 10 (1965):2813-2821, https://doi.org/10.1016/S0040-4020(01)98366-8 . .