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Volumn 132, Issue 14, 2010, Pages 5176-5178

Total synthesis of the lycorenine-type amaryllidaceae alkaloid (±)-Clivonine via a biomimetic ring-switch from a lycorine-type progenitor

Author keywords

[No Author keywords available]

Indexed keywords

AMARYLLIDACEAE; DIASTEREOSELECTIVE; TOTAL SYNTHESIS;

EID: 77950817924     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja910184j     Document Type: Article
Times cited : (18)

References (40)
  • 1
    • 61449118878 scopus 로고    scopus 로고
    • and previous reviews in this series
    • Jin, Z. Nat. Prod. Rep. 2009, 26, 363-381 and previous reviews in this series
    • (2009) Nat. Prod. Rep. , vol.26 , pp. 363381
    • Jin, Z.1
  • 5
    • 0004278356 scopus 로고
    • Birkhauser: Basel, Switzerland
    • Barton, D. R. H. Festshrift Arthur Stoll; Birkhauser: Basel, Switzerland, 1957; pp 126-129.
    • (1957) Festshrift Arthur Stoll , pp. 126-129
    • Barton, D.R.H.1
  • 6
    • 77950794020 scopus 로고
    • In, tazettine was thought to be a natural product. Later, Wildman showed it to be an artifact of isolation during which an intramolecular crossed-Cannizzaro rearrangement takes place; pretazettine is the natural product (6, 7c)
    • In 1957, tazettine was thought to be a natural product. Later, Wildman showed it to be an artifact of isolation during which an intramolecular crossed-Cannizzaro rearrangement takes place; pretazettine is the natural product (6, 7c)
    • (1957)
  • 34
    • 25444434134 scopus 로고    scopus 로고
    • Enone 6 can also be prepared in enantiomerically pure form [(5 S, 6 S)-(+)- 6 ] via Pseudomonas putida microbial oxidation of chlorobenzene, see:, Reference 18a
    • Enone 6 can also be prepared in enantiomerically pure form [(5 S, 6 S)-(+)- 6 ] via Pseudomonas putida microbial oxidation of chlorobenzene, see: Spivey, A. C., Giró Manñas, C., and Mann, I. Chem. Commun. 2005, 4426-4428 Reference 18a.
    • (2005) Chem. Commun. , pp. 4426-4428
    • Spivey, A.C.1    Giró Manñas, C.2    Mann, I.3
  • 40
    • 77950803606 scopus 로고    scopus 로고
    • The isolated yields of these alkaloid constituents show strong seasonal dependence (e.g., ref 8)
    • The isolated yields of these alkaloid constituents show strong seasonal dependence (e.g., ref 8).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.