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Volumn 12, Issue 17, 2010, Pages 3906-3909

Development of a 2-aza-cope-[3 + 2] dipolar cycloaddition strategy for the synthesis of quaternary proline scaffolds

Author keywords

[No Author keywords available]

Indexed keywords

DRUG DERIVATIVE; PROLINE; PYRROLIDINE DERIVATIVE;

EID: 77956218622     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol101606v     Document Type: Article
Times cited : (16)

References (44)
  • 1
    • 77956214019 scopus 로고    scopus 로고
    • For reviews of these alkaloid classses, see
    • For reviews of these alkaloid classses, see
  • 3
    • 0001465266 scopus 로고
    • Ed.; Academic Press: New York
    • Martin, S. F. In The Alkaloids; Brossi, A., Ed.; Academic Press: New York, 1987; Vol. 30, p 252.
    • (1987) The Alkaloids , vol.30 , pp. 252
    • Martin, S.F.1    Brossi, A.2
  • 4
    • 77956218705 scopus 로고    scopus 로고
    • Ed.; Academic Press: New York. For selected syntheses, see
    • Tsuda, Y.; Sano, T. In The Alkaloids; Cordell, G. A., Ed.; Academic Press: New York, 1996; Vol. 48, p 239. For selected syntheses, see
    • (1996) The Alkaloids , vol.48 , pp. 239
    • Tsuda, Y.1    Sano, T.2    Cordell, G.A.3
  • 15
    • 77956214501 scopus 로고    scopus 로고
    • For a recent perspective, see
    • For a recent perspective, see
  • 17
    • 77956194914 scopus 로고    scopus 로고
    • For earlier accounts, see
    • For earlier accounts, see
  • 20
    • 77956205578 scopus 로고    scopus 로고
    • For selected examples, see
    • For selected examples, see
  • 35
    • 77956213200 scopus 로고    scopus 로고
    • Preparation of 1a, 1b, and 1e
    • Preparation of 1a, 1b, and 1e
  • 37
    • 77956212545 scopus 로고    scopus 로고
    • Preparation of 1d
    • Preparation of 1d
  • 40
    • 77956210601 scopus 로고    scopus 로고
    • For the preparation of 1c, see Supporting Information
    • For the preparation of 1c, see Supporting Information.
  • 41
    • 77956203223 scopus 로고    scopus 로고
    • We found it convenient to conduct the reactions in the presence of 4 Å molecular sieves, thereby reducing the possibility of byproduct formation from competing processes with water
    • We found it convenient to conduct the reactions in the presence of 4 Å molecular sieves, thereby reducing the possibility of byproduct formation from competing processes with water.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.