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Volumn 39, Issue 10, 2000, Pages 1829-1832

The absolute configuration and asymmetric total synthesis of the CP molecules (CP-263,114 and CP-225,917, phomoidrides B and A)

Author keywords

Asymmetric synthesis; Configuration determination; Natural products; Polycycles; Total synthesis

Indexed keywords

ALDEHYDE; ORGANIC COMPOUND; PHOMOIDRIDE A; PHOMOIDRIDE B; UNCLASSIFIED DRUG;

EID: 0034658143     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3773(20000515)39:10<1829::AID-ANIE1829>3.0.CO;2-6     Document Type: Article
Times cited : (69)

References (49)
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    • Catalyst 4 was prepared from the corresponding (S)-diol and Al(iBu3) (1.0 equiv, 1.0 M in hexanes) by stirring the two compounds in toluene at ambient temperature for 30 min. The diol was prepared according to the methods of K. B. Simonsen, K. V. Gothelf, K. A. Jørgensen, J. Org. Chem. 1998, 63, 7536 and P. Wipf and J.-K. Jung (see J.-K. Jung, Ph.D. Thesis, University of Pittsburgh, 1999).
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    • Catalyst 4 was prepared from the corresponding (S)-diol and Al(iBu3) (1.0 equiv, 1.0 M in hexanes) by stirring the two compounds in toluene at ambient temperature for 30 min. The diol was prepared according to the methods of K. B. Simonsen, K. V. Gothelf, K. A. Jørgensen, J. Org. Chem. 1998, 63, 7536 and P. Wipf and J.-K. Jung (see J.-K. Jung, Ph.D. Thesis, University of Pittsburgh, 1999).
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    • note
    • 2 (1M in hexanes) to a solution of the corresponding phenol (1.1 equiv) in toluene at 0 C and stirring the mixture at ambient temperature for 30 min.
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    • note
    • 2, in aqueous methanol (71 %).
  • 47
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    • note
    • 2, 25 C.
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    • note
    • A sample of natural 1 was kindly provided to us by Dr. T. Kaneko, Pfizer (Groton, CT).
  • 49
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    • note
    • A similar effect was observed for (-)-16 and (+)-16.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.