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Volumn 65, Issue 4, 2009, Pages 888-895

Alternative synthetic approach for (+)-phomopsidin via the highly stereoselective TADA reaction

Author keywords

[No Author keywords available]

Indexed keywords

FUNGAL PROTEIN; KETONE DERIVATIVE; LACTONE DERIVATIVE; MICROTUBULE PROTEIN; PHOMOPSIDIN; UNCLASSIFIED DRUG;

EID: 57649089188     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.11.030     Document Type: Article
Times cited : (16)

References (26)
  • 4
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    • Wakui, F.; Harimaya, K.; Iwata, M.; Sashita, R.; Chiba, N.; Mikawa, T. Jpn. Kokai Tokkyo Koho JP 07,126,211, May 16, 1995, Appl. Oct. 29, 1993;
    • Wakui, F.; Harimaya, K.; Iwata, M.; Sashita, R.; Chiba, N.; Mikawa, T. Jpn. Kokai Tokkyo Koho JP 07,126,211, May 16, 1995, Appl. Oct. 29, 1993;
  • 5
    • 4243622054 scopus 로고
    • Chem. Abstr. 123 (1995) 105272b
    • (1995) Chem. Abstr. , vol.123
  • 7
    • 0000048482 scopus 로고
    • For reviews, see:. Trost B.M., and Fleming I. (Eds), Pergamon, Oxford and references cited therein and in Ref. 7
    • For reviews, see:. Roush W.R. In: Trost B.M., and Fleming I. (Eds). Comprehensive Organic Synthesis Vol. 5 (1991), Pergamon, Oxford 513-550 and references cited therein and in Ref. 7
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 513-550
    • Roush, W.R.1
  • 11
    • 0000454316 scopus 로고
    • The same stereoelectronic effect reported by Deslongchamps and co-workers: Our contribution to the stereoselective IMDA reactions that would be influenced by the allylic stereogenic center with a hydroxyl group, see:
    • The same stereoelectronic effect reported by Deslongchamps and co-workers:. Dory Y.L., Ouellet C., Berthiaume S., Favre A., and Deslongchamps P. Bull. Soc. Chim. Fr. 131 (1994) 121-141 Our contribution to the stereoselective IMDA reactions that would be influenced by the allylic stereogenic center with a hydroxyl group, see:
    • (1994) Bull. Soc. Chim. Fr. , vol.131 , pp. 121-141
    • Dory, Y.L.1    Ouellet, C.2    Berthiaume, S.3    Favre, A.4    Deslongchamps, P.5
  • 17
    • 2042507954 scopus 로고
    • and references cited therein
    • Miyaura N., and Suzuki A. Chem. Rev. 95 (1995) 2457-2483 and references cited therein
    • (1995) Chem. Rev. , vol.95 , pp. 2457-2483
    • Miyaura, N.1    Suzuki, A.2
  • 23
    • 57649091068 scopus 로고    scopus 로고
    • note
    • Most of the geometrical isomer of the macrolactone 5 remained unreacted.
  • 24
    • 57649111430 scopus 로고    scopus 로고
    • note
    • The ratio was based on the weight of the products.
  • 25
    • 0002446724 scopus 로고
    • Trost B.M., and Fleming I. (Eds), Pergamon, Oxford and references cited therein
    • Roush W.R. In: Trost B.M., and Fleming I. (Eds). Comprehensive Organic Synthesis Vol. 8 (1991), Pergamon, Oxford 1-24 and references cited therein
    • (1991) Comprehensive Organic Synthesis , vol.8 , pp. 1-24
    • Roush, W.R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.