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Synthesis of optically active, cyclic alpha-hydroxy ketones and 1,2-diketones from verbenone epoxide Full article

Journal Helvetica Chimica Acta
ISSN: 0018-019X , E-ISSN: 1522-2675
Output data Year: 2006, Volume: 89, Number: 3, Pages: 507-514 Pages count : DOI: 10.1002/hlca.200690052
Authors Il'ina IV , Volcho KP , Korchagina DV , Barkhash VA , Salakhutdinov NF
Affiliations
1 (Данные Web of science) Russian Acad Sci, NN Vorozhtsov Novosibirsk Inst Organ Chem, Siberian Branch, Novosibirsk 630090, Russia

Abstract: The reactivity of verbenone epoxide (5), a terpenoid from the pinane series, towards different aliphatic and aromatic aldehydes in the presence of natural montmorillonite (askanite-bentonite) clay has been studied. A series of mechanistically different transformations afforded a number of new, optically active, polyfunctional compounds (7, 8, 10 - 14, 16). These products are potentially interesting synthons in asymmetric synthesis.
Cite: Il'ina I. , Volcho K. , Korchagina D. , Barkhash V. , Salakhutdinov N.
Synthesis of optically active, cyclic alpha-hydroxy ketones and 1,2-diketones from verbenone epoxide
Helvetica Chimica Acta. 2006. V.89. N3. P.507-514. DOI: 10.1002/hlca.200690052 WOS Scopus РИНЦ OpenAlex
Dates:
Published print: Mar 1, 2006
Identifiers:
Web of science: WOS:000236535500013
Scopus: 2-s2.0-33645580391
Elibrary: 13505982
OpenAlex: W2027871678
Citing:
DB Citing
Web of science 24
Scopus 23
Elibrary 27
OpenAlex 20
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