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Volumn 2, Issue 15, 2000, Pages 2189-2192

Control of olefin geometry in the bryostatin B-ring through exploitation of a C2-symmetry breaking tactic and a Smith-Tietze coupling reaction

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; ANTINEOPLASTIC AGENT; BRYOSTATIN 1; EPOXIDE; ETHER DERIVATIVE; KETONE; LACTONE; MACROLIDE;

EID: 0034720959     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol005850y     Document Type: Article
Times cited : (48)

References (51)
  • 4
    • 0000575874 scopus 로고
    • (a) For the total synthesis of bryostatin 7, see: Masamune, S. Pure Appl. Chem. 1988, 60, 1587. Kageyama, M.; Tamura, T.; Nantz, M. H.; Roberts, J. C.; Somfai, P.; Whritenour, D. C.; Masamune, S. J. Am. Chem. Soc. 1990, 112, 7407.
    • (1988) Pure Appl. Chem. , vol.60 , pp. 1587
    • Masamune, S.1
  • 45
    • 0042507985 scopus 로고
    • For the use of a Reformatsky reaction/dehydration sequence to create an exocyclic enoate, see: Johnson, W. S.; Christianson, R. G. J. Am. Chem. Soc. 1951, 73, 5511.
    • (1951) J. Am. Chem. Soc. , vol.73 , pp. 5511
    • Johnson, W.S.1    Christianson, R.G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.