Synthesis of Derivatives of the Optically Active beta-Amino Acids from (+)-Car-2-ene Full article
Journal |
Helvetica Chimica Acta
ISSN: 0018-019X , E-ISSN: 1522-2675 |
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Output data | Year: 2008, Volume: 91, Number: 10, Pages: 1849-1856 Pages count : DOI: 10.1002/hlca.200890197 | ||
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Abstract:
The reaction of (+)-car-2-ene (4) with chlorosulfonyl isocyanate (=sulfuryl chloride isocyanate; CISO2NCO) led to the tricyclic lactams 6 and 8 corresponding to the initial formation both of the tertiary carbenium and alpha-cyclopropylcarbenium ions (Scheme 2). A number of optically active derivatives of beta-amino acids which are promising compounds for further use in asymmetric synthesis were synthesized from the lactams (see 16, 17, and 19-21 in Scheme 3).
Cite:
Koneva E.A.
, Volcho K.P.
, Gatilov Y.V.
, Korchagina D.V.
, Salnikov G.E.
, Salakhutdinov N.F.
Synthesis of Derivatives of the Optically Active beta-Amino Acids from (+)-Car-2-ene
Helvetica Chimica Acta. 2008. V.91. N10. P.1849-1856. DOI: 10.1002/hlca.200890197 WOS Scopus РИНЦ
Synthesis of Derivatives of the Optically Active beta-Amino Acids from (+)-Car-2-ene
Helvetica Chimica Acta. 2008. V.91. N10. P.1849-1856. DOI: 10.1002/hlca.200890197 WOS Scopus РИНЦ
Dates:
Published print: | Oct 1, 2008 |
Identifiers:
Web of science | WOS:000261050300004 |
Scopus | 2-s2.0-55249104742 |
Elibrary | 13567262 |
OpenAlex | W2038120370 |