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Volumn 127, Issue 50, 2005, Pages 17921-17937

Ru-catalyzed alkene-alkyne coupling. Total synthesis of amphidinolide P

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; CHELATION; COMPLEXATION; RUTHENIUM; SATURATION (MATERIALS COMPOSITION); SYNTHESIS (CHEMICAL); THERMODYNAMICS;

EID: 29344448010     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja055967n     Document Type: Article
Times cited : (93)

References (142)
  • 11
    • 7044233499 scopus 로고    scopus 로고
    • For the most recent studies, see, Amphidinolide F: (a) Shotwell, J. B.; Roush, W. R. Org. Lett. 2004, 6, 3865.
    • (2004) Org. Lett. , vol.6 , pp. 3865
    • Shotwell, J.B.1    Roush, W.R.2
  • 39
    • 29344470821 scopus 로고    scopus 로고
    • ref 5c, 5e, 5f
    • (h) ref 5c, 5e, 5f.
  • 45
    • 29344436858 scopus 로고    scopus 로고
    • ref 6g
    • (c) ref 6g.
  • 57
    • 0001055858 scopus 로고    scopus 로고
    • Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer-Verlag: Heidelberg, Chapter 27
    • (a) Yanagisawa, A. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer-Verlag: Heidelberg, 1999; Vol. 2, Chapter 27.
    • (1999) Comprehensive Asymmetric Catalysis , vol.2
    • Yanagisawa, A.1
  • 81
    • 0000912070 scopus 로고    scopus 로고
    • Racemic aldehyde 28a was prepared by dihydroxylation, followed by oxidative cleavage of known PMB-protected hepta-1,6-dien-4-o1: Shepherd, J. N.; Na, J.; Myles, D. C. J. Org. Chem. 1997, 62, 4558.
    • (1997) J. Org. Chem. , vol.62 , pp. 4558
    • Shepherd, J.N.1    Na, J.2    Myles, D.C.3
  • 82
    • 85046172650 scopus 로고    scopus 로고
    • Racemic aldehyde 28b was prepared in four standard steps (allylation, TBS protection, DDQ-mediated PMB cleavage, and Moffat-Swern oxidation) from known 3-(4-methoxy-benzyloxy)-propionaldehyde: Oka, T.; Marai, A. Tetrahedron 1998, 54, 1.
    • (1998) Tetrahedron , vol.54 , pp. 1
    • Oka, T.1    Marai, A.2
  • 86
    • 29344451261 scopus 로고    scopus 로고
    • note
    • See the Supporting Information for details.
  • 87
    • 29344468056 scopus 로고    scopus 로고
    • note
    • 2 in dichloromethane gave a 1:1 1,2-anti/syn ratio and an 8:1 2,4-anti/syn ratio. Tn both cases, alternative conditions gave higher 1,2-anti/syn ratio.
  • 91
    • 0027230283 scopus 로고
    • and references therein
    • Kant, J. J. Org. Chem. 1993, 58, 2296 and references therein.
    • (1993) J. Org. Chem. , vol.58 , pp. 2296
    • Kant, J.1
  • 106
    • 29344448282 scopus 로고    scopus 로고
    • (c) http://www.glasscontour.com/.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.