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Volumn 14, Issue 13, 2003, Pages 1787-1798

Stereochemical assignment of the C23-C35 portion of sphinxolide/reidispongiolide class of natural products by asymmetric synthesis

Author keywords

[No Author keywords available]

Indexed keywords

LACTONE DERIVATIVE; MACROLIDE; REIDISPONGIOLIDE A; SPHINXOLIDE; UNCLASSIFIED DRUG;

EID: 0037756812     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(03)00372-0     Document Type: Article
Times cited : (31)

References (24)
  • 21
    • 0034644383 scopus 로고    scopus 로고
    • The diastereomeric purity of aldol adduct 14 was judged by the NMR spectra and the configuration was assigned on the basis of literature precedent, see:
    • The diastereomeric purity of aldol adduct 14 was judged by the NMR spectra and the configuration was assigned on the basis of literature precedent, see: Smith A.B. III, Beauchamp T.J., LaMarche M.J., Kaufman M.D., Qiu Y., Arimoto H., Jones D.R., Kobayashi K. J. Am. Chem. Soc. 122:2000;8654-8664.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 8654-8664
    • Smith A.B. III1    Beauchamp, T.J.2    LaMarche, M.J.3    Kaufman, M.D.4    Qiu, Y.5    Arimoto, H.6    Jones, D.R.7    Kobayashi, K.8
  • 22
    • 0025128154 scopus 로고
    • The extraordinary level of substrate control exhibited by aldehyde 16 in the reaction with (E)-crotylboronates is quite surprising and deserves further investigation; see:
    • The extraordinary level of substrate control exhibited by aldehyde 16 in the reaction with (E)-crotylboronates is quite surprising and deserves further investigation; see: Roush W.R., Palkowitz A.D., Ando K. J. Am. Chem. Soc. 112:1990;6348-6359.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 6348-6359
    • Roush, W.R.1    Palkowitz, A.D.2    Ando, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.