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Volumn 129, Issue 4, 2007, Pages 914-923

Preparation of chiral α-oxy-[2H1]methyllithiums of 99% ee and determination of their configurational stability

Author keywords

[No Author keywords available]

Indexed keywords

BENZALDEHYDE; CHEMICAL STABILITY; METHYLLITHIUMS; SPECTROSCOPIC COMPARISON;

EID: 33846646631     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja066183s     Document Type: Article
Times cited : (40)

References (59)
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    • Organolithiums: Selectivity for Synthesis
    • Pergamon: Amsterdam
    • (b) Clayden, J. Organolithiums: Selectivity for Synthesis; Tetrahedron Organic Chemistry Series 23; Pergamon: Amsterdam, 2002.
    • (2002) Tetrahedron Organic Chemistry Series , vol.23
    • Clayden, J.1
  • 3
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    • Organolithiums in Enantioselective Synthesis; Hodgson, D. M., Ed.; Topics in Organometallic Chemistry 5; Springer: Berlin, 2003.
    • (c) Organolithiums in Enantioselective Synthesis; Hodgson, D. M., Ed.; Topics in Organometallic Chemistry 5; Springer: Berlin, 2003.
  • 18
    • 33846623819 scopus 로고    scopus 로고
    • Hoppe, D.; Marr, F.; Bruggemann, M. In Organolithiums in Enantioselective Synthesis; Hodgson, D. M., Ed.; Topics in Organometallic Chemisty 5; Springer: Berlin, 2003; pp 61-137.
    • (b) Hoppe, D.; Marr, F.; Bruggemann, M. In Organolithiums in Enantioselective Synthesis; Hodgson, D. M., Ed.; Topics in Organometallic Chemisty 5; Springer: Berlin, 2003; pp 61-137.
  • 19
    • 33846563047 scopus 로고    scopus 로고
    • Reviews: (a) Beak, P.; Johnson, T. A.; Kim, D. D.; Lim, S. H. In Organolithiums in Enantioselective Synthesis; Hodgson, D. M., Ed.; Topics in Organometallic Chemisty 5; Springer: Berlin, 2003; pp 139-176.
    • Reviews: (a) Beak, P.; Johnson, T. A.; Kim, D. D.; Lim, S. H. In Organolithiums in Enantioselective Synthesis; Hodgson, D. M., Ed.; Topics in Organometallic Chemisty 5; Springer: Berlin, 2003; pp 139-176.
  • 44
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    • Chem. Abstr. 1953, 47, 3227i.
    • Chem. Abstr. 1953, 47, 3227i.
  • 46
    • 33846611514 scopus 로고    scopus 로고
    • The analogue compound formed from the TMP derivative was isolated in 2% as a side product when carbamate 28 was stannylated according to Scheme 7.
    • The analogue compound formed from the TMP derivative was isolated in 2% as a side product when carbamate 28 was stannylated according to Scheme 7.
  • 49
    • 33846585555 scopus 로고    scopus 로고
    • v. d. Kerk, G. J. M.; Noltes, J. G.; Luijten, J. G. A. J. Appl. Chem. 1957, 7, 366-369.
    • v. d. Kerk, G. J. M.; Noltes, J. G.; Luijten, J. G. A. J. Appl. Chem. 1957, 7, 366-369.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.