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Volumn 44, Issue 7, 2003, Pages 1343-1346

Reaction of lithium eneselenolates derived from selenoamides with ketones: A highly diastereoselective synthetic route to β,β-disubstituted β-hydroxy selenoamides

Author keywords

, disubstituted hydroxy selenoamides; Diastereoselectivity; Lithium eneselenolates; Organoselenium compounds; Selenoamides

Indexed keywords

AMIDE; CYCLOHEXANE OXIDE; KETONE DERIVATIVE; LITHIUM DERIVATIVE;

EID: 0037429087     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)02877-0     Document Type: Article
Times cited : (25)

References (35)
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    • (a) Heathcock, C. H. Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I., Eds.; Pergamon, Oxford, 1991; Vol. 2, p. 181;
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 181
    • Heathcock, C.H.1
  • 2
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    • Page P. C. B., Ed.; Springer: Berlin
    • (b) Metzner, P. In Topics in Current Chemistry; Page P. C. B., Ed.; Springer: Berlin, 1999; Vol. 204, p. 127.
    • (1999) Topics in Current Chemistry , vol.204 , pp. 127
    • Metzner, P.1
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    • 0342531366 scopus 로고    scopus 로고
    • Back, T. G., Ed.; Oxford University Press: Oxford
    • (c) Chieffi, A.; Comasseto, J. V. Organoselenium Chemistry; Back, T. G., Ed.; Oxford University Press: Oxford, 1999; p. 131;
    • (1999) Organoselenium Chemistry , pp. 131
    • Chieffi, A.1    Comasseto, J.V.2
  • 11
    • 0001600151 scopus 로고    scopus 로고
    • Wirth, T., Ed.; Springer: Berlin
    • (d) Murai, T.; Kato, S. Topics in Current Chemistry; Wirth, T., Ed.; Springer: Berlin, 2000; Vol. 208, p. 177;
    • (2000) Topics in Current Chemistry , vol.208 , pp. 177
    • Murai, T.1    Kato, S.2
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    • and references cited therein.
    • Murai T., Aso H., Kato S. Org. Lett. 4:2002;1407. and references cited therein.
    • (2002) Org. Lett. , vol.4 , pp. 1407
    • Murai, T.1    Aso, H.2    Kato, S.3
  • 27
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    • 2O as an eluent to give 0.171 g (70%) of 4a as a yellow oil.
    • 2O as an eluent to give 0.171 g (70%) of 4a as a yellow oil.
  • 28
    • 0012926255 scopus 로고    scopus 로고
    • 1=0.057, 1271 reflections, GOF=1.00. Crystallographic Data for 4h have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC 197594.
    • 1=0.057, 1271 reflections, GOF=1.00. Crystallographic Data for 4h have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC 197594.
  • 29
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    • The signals due to the carbon atom of the C=Se group of anti isomers were observed in higher fields than those of syn isomers.
    • The signals due to the carbon atom of the C=Se group of anti isomers were observed in higher fields than those of syn isomers.
  • 30
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    • 5c
    • 5c.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.