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Volumn 47, Issue 37, 2008, Pages 7091-7094

Total synthesis of pinnatoxin A

Author keywords

Cyclization; Cycloaddition; Macrocycles; Natural products; Ruthenium

Indexed keywords


EID: 54749088233     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200802729     Document Type: Article
Times cited : (41)

References (59)
  • 6
    • 21644490169 scopus 로고    scopus 로고
    • For a review, see
    • For a review, see: M. Kita, D. Uemura, Chem. Lett. 2005, 34, 454-459.
    • (2005) Chem. Lett , vol.34 , pp. 454-459
    • Kita, M.1    Uemura, D.2
  • 10
    • 33745028358 scopus 로고    scopus 로고
    • Kishi and co-workers also reported the total syntheses and stereochemistry of pinnatoxins B, C, and pteriatoxins A-C: c F. Matsuura, R. Peters, M. Anada, S. S. Harried, J. Hao, Y. Kishi, J. Am. Chem. Soc. 2006, 128, 7463-7465;
    • Kishi and co-workers also reported the total syntheses and stereochemistry of pinnatoxins B, C, and pteriatoxins A-C: c) F. Matsuura, R. Peters, M. Anada, S. S. Harried, J. Hao, Y. Kishi, J. Am. Chem. Soc. 2006, 128, 7463-7465;
  • 14
    • 11144270139 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 6505-6510.
    • (2004) Angew. Chem. Int. Ed , vol.43 , pp. 6505-6510
  • 15
    • 0002504638 scopus 로고    scopus 로고
    • For synthetic studies on pinnatoxin A by the Hirama group, see: a
    • For synthetic studies on pinnatoxin A by the Hirama group, see: a) T. Noda, A. Ishiwata, S. Uemura, S. Sakamoto, M. Hirama, Synlett 1998, 298-300;
    • (1998) Synlett , pp. 298-300
    • Noda, T.1    Ishiwata, A.2    Uemura, S.3    Sakamoto, S.4    Hirama, M.5
  • 20
    • 17844381003 scopus 로고    scopus 로고
    • For synthetic studies on pinnatoxin A by the Zakarian group, see: a
    • For synthetic studies on pinnatoxin A by the Zakarian group, see: a) M. J. Pelc, A. Zakarian, Org. Lett. 2005, 7, 1629-1631;
    • (2005) Org. Lett , vol.7 , pp. 1629-1631
    • Pelc, M.J.1    Zakarian, A.2
  • 38
    • 0025164552 scopus 로고
    • For the use of α-methylenelactones in Diels-Alder reactions, see: a
    • For the use of α-methylenelactones in Diels-Alder reactions, see: a) F. Fotiadu, F. Michel, G. Buono, Tetrahedron Lett. 1990, 31, 4863-4866;
    • (1990) Tetrahedron Lett , vol.31 , pp. 4863-4866
    • Fotiadu, F.1    Michel, F.2    Buono, G.3
  • 45
    • 27544502994 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 6630-6666.
    • (2005) Angew. Chem. Int. Ed , vol.44 , pp. 6630-6666
  • 46
    • 1942489377 scopus 로고    scopus 로고
    • For the use of cycloisomerizations to construct the macrocycles, see: a
    • For the use of cycloisomerizations to construct the macrocycles, see: a) B. M. Trost, P. E. Harrington, J. Am. Chem. Soc. 2004, 126, 5028-5029;
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 5028-5029
    • Trost, B.M.1    Harrington, P.E.2
  • 50
    • 54749104315 scopus 로고    scopus 로고
    • [17] with lithiated dimethyl methylphosphonate in THF at -78°C for 30 min.
    • [17] with lithiated dimethyl methylphosphonate in THF at -78°C for 30 min.
  • 54
    • 0038568793 scopus 로고    scopus 로고
    • 2H as the hydrogen donor in transfer hydrogenolysis, see: a B. ElAmin, G. M. Anantharamaiah, G. P. Royer, G. E. Means, J. Org. Chem. 1979, 44, 3442-3444;
    • 2H as the hydrogen donor in transfer hydrogenolysis, see: a) B. ElAmin, G. M. Anantharamaiah, G. P. Royer, G. E. Means, J. Org. Chem. 1979, 44, 3442-3444;


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.