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Volumn 74, Issue 6, 2009, Pages 2624-2626

Formal total synthesis of haouamine A

Author keywords

[No Author keywords available]

Indexed keywords

MIZOROKI-HECK REACTIONS; TOTAL SYNTHESIS;

EID: 64149116082     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo802787j     Document Type: Article
Times cited : (22)

References (26)
  • 2
    • 33645450011 scopus 로고    scopus 로고
    • For the total synthesis of (±)-haouamine
    • For the total synthesis of (±)-haouamine A. see: Baran, P. S.; Burns, N. Z. J. Am. Chem.Soc 2006, 128, 3908.
    • (2006) J. Am. Chem.Soc , vol.128 , pp. 3908
    • see, A.1    Baran, P.S.2    Burns, N.Z.3
  • 3
    • 37549003646 scopus 로고    scopus 로고
    • This paper also corrected the biosynthesis proposed in ref 4. For the total synthesis of, -haouamine
    • For the total synthesis of (+)-haouamine A, see: Baran, P. S.; Burns, N. Z. Angew. Chem. Int. Ed. 2008, 47, 205. This paper also corrected the biosynthesis proposed in ref 4.
    • (2008) Angew. Chem. Int. Ed , vol.47 , pp. 205
    • see, A.1    Baran, P.S.2    Burns, N.Z.3
  • 5
    • 33745725813 scopus 로고    scopus 로고
    • For the formal synthesis of haouamine A, see: (a) J, H; Jeong, S. M.; Weinreb, Org. Lett. 2006, 8, 2309.
    • For the formal synthesis of haouamine A, see: (a) J, H; Jeong, S. M.; Weinreb, Org. Lett. 2006, 8, 2309.
  • 7
    • 26444561793 scopus 로고    scopus 로고
    • For synthetic studies toward haouamines, see: a
    • For synthetic studies toward haouamines, see: (a) Smith. N. D; Hayashida, J.; Rawal, V. H. Qrg. Lett. 2005, 7, 4309.
    • (2005) Qrg. Lett , vol.7 , pp. 4309
    • Smith, N.D.1    Hayashida, J.2    Rawal, V.H.3
  • 11
    • 0042379984 scopus 로고    scopus 로고
    • For reviews on palladium-catalyzed reactions involving the Mizoroki-Heck reaction, see: a
    • For reviews on palladium-catalyzed reactions involving the Mizoroki-Heck reaction, see: (a) Dounau, A. B.; Overman, L. E. Chem. Rev. 2003, 103, 2945.
    • (2003) Chem. Rev , vol.103 , pp. 2945
    • Dounau, A.B.1    Overman, L.E.2
  • 19
    • 64149107453 scopus 로고    scopus 로고
    • The cinnamyl group in compound 8 was chosen so as to avoid the isomerization of exo olefin into endo olefin after the cyclization of 8.
    • The cinnamyl group in compound 8 was chosen so as to avoid the isomerization of exo olefin into endo olefin after the cyclization of 8.
  • 20
    • 2042507954 scopus 로고
    • For a review on Suzuki-Miyaura coupling, see
    • For a review on Suzuki-Miyaura coupling, see: Miyaura, N.; Suzuki, A. Chem. Rev. 1995, 95, 2457.
    • (1995) Chem. Rev , vol.95 , pp. 2457
    • Miyaura, N.1    Suzuki, A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.