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Volumn 2010, Issue 2, 2010, Pages 1-15

Dynamic kinetic resolution of (S)-mandelate-derived á-bromo esters in nucleophilic substitution and asymmetric syntheses of 3-substituted morpholin-2-ones

Author keywords

Asymmetric synthesis; Chiral auxiliary; Dynamic kinetic resolution; Morpholinone; Nucleophilic substitution

Indexed keywords


EID: 77953407637     PISSN: 1551-7012     EISSN: 15517004     Source Type: Journal    
DOI: 10.3998/ark.5550190.0011.201     Document Type: Article
Times cited : (8)

References (22)
  • 1
    • 0027205525 scopus 로고
    • For reviews on pantolactone auxiliary, see: a
    • For reviews on pantolactone auxiliary, see: (a) Koh, K.; Ben, R. N.; Durst, T. Tetrahedron Lett. 1993, 34, 4473.
    • (1993) Tetrahedron. Lett. , vol.34 , pp. 4473
    • Koh, K.1    Ben, R.N.2    Durst, T.3
  • 16
    • 85069135757 scopus 로고    scopus 로고
    • the reference 3c, Devine et al reported that no spontaneous cyclization was observed in the reactions of lactamide-derived α-halo phenylacetates with N-benzyl 2-aminoethanol. Also, we found that reactions of α-substituted methyl α-bromo acetates with N-benzyl 2-aminoethanol did not gave the cyclized products
    • In the reference 3c, Devine et al reported that no spontaneous cyclization was observed in the reactions of lactamide-derived α-halo phenylacetates with N-benzyl 2-aminoethanol. Also, we found that reactions of α-substituted methyl α-bromo acetates with N-benzyl 2-aminoethanol did not gave the cyclized products.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.