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Volumn 46, Issue 35, 2007, Pages 6703-6705

Total synthesis of neooxazolomycin

Author keywords

Alkaloids; Antibiotics; Natural products; Total synthesis

Indexed keywords

ALKALOIDS; ALKENYLATION; LACTONIZATION; NATURAL PRODUCTS;

EID: 34548628976     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200702229     Document Type: Article
Times cited : (63)

References (29)
  • 11
    • 0001539570 scopus 로고    scopus 로고
    • For a review, see, Eds, Z. Rappoport, Y. Apeloig, Wiley, New York
    • For a review, see I. Ojima, Z. Li, J. Zhu in The Chemistry of Organic Silicon Compounds, Vol. 2 (Eds.: Z. Rappoport, Y. Apeloig), Wiley, New York, 1998, pp. 1687-1792.
    • (1998) The Chemistry of Organic Silicon Compounds , vol.2 , pp. 1687-1792
    • Ojima, I.1    Li, Z.2    Zhu, J.3
  • 17
    • 34548607722 scopus 로고    scopus 로고
    • 3 (1 equiv) in EtOH at room temperature, the corresponding Z isomer was obtained exclusively in 50% yield.
    • 3 (1 equiv) in EtOH at room temperature, the corresponding Z isomer was obtained exclusively in 50% yield.
  • 20
    • 34548657678 scopus 로고    scopus 로고
    • 2O (3:1), which was the same solvent system as that employed for the osmylation.
    • 2O (3:1), which was the same solvent system as that employed for the osmylation.
  • 21
    • 34548602171 scopus 로고    scopus 로고
    • Conformer 17 was suggested to be the energetically most stable by Molecular mechanics calculations (MMFF, Macro Model 8.5).
    • Conformer 17 was suggested to be the energetically most stable by Molecular mechanics calculations (MMFF, Macro Model 8.5).
  • 24
    • 33845373603 scopus 로고    scopus 로고
    • Prepared by Takai-Utimoto olefination of (E)-4-(Fmoc)amino-but-2- enal; see the Supporting Information and also K. Takai, K. Nitta, K. Utimoto, J. Am. Chem. Soc. 1986, 108, 7408-7410.
    • Prepared by Takai-Utimoto olefination of (E)-4-(Fmoc)amino-but-2- enal; see the Supporting Information and also K. Takai, K. Nitta, K. Utimoto, J. Am. Chem. Soc. 1986, 108, 7408-7410.
  • 26
    • 34548618902 scopus 로고    scopus 로고
    • WO 2003006422
    • Y. Watanabe, WO 2003006422.
    • Watanabe, Y.1
  • 29
    • 34548641322 scopus 로고    scopus 로고
    • Prepared by a modified Kende procedure, where the method for the preparation of (Z)-2-methyl-5-(trimethylsilyl)pent-2-en-4-ynal, required for the key aldol reaction, was highly improved; see the Supporting Information.
    • Prepared by a modified Kende procedure, where the method for the preparation of (Z)-2-methyl-5-(trimethylsilyl)pent-2-en-4-ynal, required for the key aldol reaction, was highly improved; see the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.