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Volumn 17, Issue 20, 2015, Pages 5084-5087

Approach to cis-Phlegmarine Alkaloids via Stereodivergent Reduction: Total Synthesis of (+)-Serratezomine e and Putative Structure of (-)-Huperzine N

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; HUPERZINE A; QUINOLINE DERIVATIVE; SERRATEZOMINE E; SESQUITERPENE;

EID: 84944916851     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/acs.orglett.5b02581     Document Type: Article
Times cited : (21)

References (26)
  • 15
    • 84944955122 scopus 로고    scopus 로고
    • For an unsuccessful analogous reduction of the vinylpyridine unit in an approach to the alkaloid dihydrolycolucine, leading to the opposite stereochemistry to that required, see: House, S. E. Ph.D thesis, University of California, Berkeley, 2010.
    • (2010)
    • House, S.E.1
  • 22
    • 78449245989 scopus 로고    scopus 로고
    • The NMR data for the piperidine ring atoms are slightly different from those reported for the natural product. However, partial protonation of our synthetic 1 afforded NMR data identical to those described for natural 1. For a similar titration of a free base with TFA, see: Altman, R. A.; Nilsson, B. L.; Overman, L. E.; Read de Alaniz, J.; Rohde, J. M.; Taupin, V. J. Org. Chem. 2010, 75, 7519 10.1021/jo101619d
    • (2010) J. Org. Chem. , vol.75 , pp. 7519
    • Altman, R.A.1    Nilsson, B.L.2    Overman, L.E.3    Read De Alaniz, J.4    Rohde, J.M.5    Taupin, V.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.