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Volumn 8, Issue 8, 2006, Pages 1617-1620

Enantioselective synthesis and absolute configuration assignment of gabosine O. synthesis of (+)- and (-)-gabosine N and (+)- and (-)-epigabosines N and O

Author keywords

[No Author keywords available]

Indexed keywords

BENZOQUINONE DERIVATIVE; CYCLOHEXANONE DERIVATIVE; GABOSINE N;

EID: 33646445311     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol060173e     Document Type: Article
Times cited : (40)

References (24)
  • 3
    • 0034728955 scopus 로고    scopus 로고
    • Synthetic studies indicate that the structure of gabosine K needs to be revised: (c) Metha, G.; Lakshminath, S. Tetrahedron Lett. 2000, 41, 3509.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 3509
    • Metha, G.1    Lakshminath, S.2
  • 13
    • 15944370982 scopus 로고    scopus 로고
    • (e) Ramana, G. V.; Rao, B. V. Tetrahedron Lett. 2005, 46, 3049. Gabosine I: ref 3. (±)-Gabosine B and putative structure of (±)-gabosine K: ref 1c. Gabosine A:
    • (2005) Tetrahedron Lett. , vol.46 , pp. 3049
    • Ramana, G.V.1    Rao, B.V.2
  • 20
    • 0037123420 scopus 로고    scopus 로고
    • For sterically controlled facial selectivity in dihydroxylation reactions of related systems, see: Kwon, Y.-U.; Lee, C.; Ghung, S.-K. J. Org. Chem. 2002, 67, 3327.
    • (2002) J. Org. Chem. , vol.67 , pp. 3327
    • Kwon, Y.-U.1    Lee, C.2    Ghung, S.-K.3
  • 23
    • 33646461351 scopus 로고    scopus 로고
    • note
    • Enantiomeric excesses were determined by CHPLC analyses.
  • 24
    • 33646452683 scopus 로고    scopus 로고
    • note
    • 1d -21.0° (c 0.1, MeOH).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.