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Volumn 5, Issue 6, 2014, Pages 2184-2190

Total syntheses of indolactam alkaloids (-)-indolactam V, (-)-pendolmycin, (-)-lyngbyatoxin A, and (-)-teleocidin A-2

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOIDS; COUPLINGS; NITROGEN COMPOUNDS; SYNTHESIS (CHEMICAL);

EID: 84900303608     PISSN: 20416520     EISSN: 20416539     Source Type: Journal    
DOI: 10.1039/c4sc00256c     Document Type: Article
Times cited : (59)

References (81)
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    • L. Shi, US Pat., US2011152308A1, 2011
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    • Shi, L.1
  • 67
    • 84900334966 scopus 로고    scopus 로고
    • US Pat., US2013023502A1, The transformations used to prepare are identical to those previously developed in our laboratory, but with modified procedures to improve the yields. See the ESI for details. Our previously reported yield for the formation of 11 from 9 and 10 was 62%; see ref. 10 Less than 5% of the corresponding C5-substituted product was detected
    • G. Dahmann, D. Fiegen, M. Fleck, M. Hoffmann, J. Klicic, S. P. East, S. C. R. Napier and J. Scott, US Pat., US2013023502A1, 2013
    • (2013) , vol.9
    • Dahmann, G.1    Fiegen, D.2    Fleck, M.3    Hoffmann, M.4    Klicic, J.5    East, S.P.6    Napier, S.C.R.7    Scott, J.8
  • 79
    • 84900341831 scopus 로고    scopus 로고
    • US Pat., US20070072884A1
    • P. Crowley and R. Salmon, US Pat., US20070072884A1, 2007
    • (2007)
    • Crowley, P.1    Salmon, R.2
  • 80
    • 17744378379 scopus 로고    scopus 로고
    • The addition of LiBr helped to suppress the competitive formation of des-bromo compound 14 The stereochemical configurations at the newly formed quaternary centers of 31 and 32 were assigned after conversion to the natural products 3 and 4
    • N. K. Garg D. D. Caspi B. M. Stoltz J. Am. Chem. Soc. 2005 127 5970 5978
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 5970-5978
    • Garg, N.K.1    Caspi, D.D.2    Stoltz, B.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.