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Volumn 48, Issue 18, 2009, Pages 3221-3223

Catalysis in the total synthesis of bryostatin 16

Author keywords

[No Author keywords available]

Indexed keywords

MACRO-CYCLIZATION; MACROCYCLES; SUBSTRATE ACTIVATION; TOTAL SYNTHESIS;

EID: 70349934208     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200900109     Document Type: Article
Times cited : (6)

References (20)
  • 2
    • 70349940992 scopus 로고    scopus 로고
    • A. Gradillas, J. Pérez-Castells, Angew. Chem. 2006, 118, 6232-6247; Angew. Chem. Int. Ed. 2006, 45, 6086-6101.
    • A. Gradillas, J. Pérez-Castells, Angew. Chem. 2006, 118, 6232-6247; Angew. Chem. Int. Ed. 2006, 45, 6086-6101.
  • 3
    • 70349971306 scopus 로고    scopus 로고
    • Other well-known macrocyclization methods are encountered, but less frequently, for example, Horner-Wadsworth-Emmons, Nozaki-Hiyama-Kishi, and intramolecular cross-coupling
    • Other well-known macrocyclization methods are encountered, but less frequently, for example, Horner-Wadsworth-Emmons, Nozaki-Hiyama-Kishi, and intramolecular cross-coupling.
  • 5
    • 0035984562 scopus 로고    scopus 로고
    • For a review on the chemistry and biology of the bryostatins, see
    • For a review on the chemistry and biology of the bryostatins, see: K. J. Hale, M. G. Hummersone, S. Manaviazar, M. Frigerio, Nat. Prod. Rep. 2002, 19, 413-453.
    • (2002) Nat. Prod. Rep , vol.19 , pp. 413-453
    • Hale, K.J.1    Hummersone, M.G.2    Manaviazar, S.3    Frigerio, M.4
  • 7
    • 70349964242 scopus 로고    scopus 로고
    • For current information, see
    • For current information, see http://clinicaltrials.gov.
  • 11
    • 70349964234 scopus 로고    scopus 로고
    • for bryostatin 3, see: K. Ohmori, Y. Ogawa, T. Obitsu, Y. Ishikawa, S. Nishiyama, S. Yamamura, Angew. Chem. 2000, 112, 2376-2379; Angew. Chem. Int. Ed. 2000, 39, 2290-2294.
    • c) for bryostatin 3, see: K. Ohmori, Y. Ogawa, T. Obitsu, Y. Ishikawa, S. Nishiyama, S. Yamamura, Angew. Chem. 2000, 112, 2376-2379; Angew. Chem. Int. Ed. 2000, 39, 2290-2294.
  • 12
    • 44349096284 scopus 로고    scopus 로고
    • For a fascinating Prins-driven macrocyclization strategy toward bryostatin analogues, see
    • For a fascinating Prins-driven macrocyclization strategy toward bryostatin analogues, see: P. A. Wender, B. A. DeChristopher, A. J. Schrier, J. Am. Chem. Soc. 2008, 130, 6658-6659.
    • (2008) J. Am. Chem. Soc , vol.130 , pp. 6658-6659
    • Wender, P.A.1    DeChristopher, B.A.2    Schrier, A.J.3
  • 19
    • 70349950388 scopus 로고    scopus 로고
    • Trost et al. previously described a 16-step synthesis of 8 from (R)-pantolactone; see: reference [11].
    • Trost et al. previously described a 16-step synthesis of 8 from (R)-pantolactone; see: reference [11].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.