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Volumn , Issue 1, 1997, Pages 61-67

A flexible synthesis of azasugars and homoazasugars via olefin metathesis

Author keywords

azasugars; homoazasugars; olefin metathesis; ring closing olefin metathesis

Indexed keywords

CARBOHYDRATE DERIVATIVE; POLYOL; PYRROLIDINE DERIVATIVE;

EID: 0031039168     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1997-1497     Document Type: Article
Times cited : (88)

References (27)
  • 3
    • 0029163690 scopus 로고
    • For example see: Wong, C.-H.; Halcomb, R. L.; Ichikawa, Y.; Kajimoto; T. Angew. Chem. 1995, 107, 569; Angew. Chem., Int. Ed. Engl. 1995, 34, 521. Legler, G. Naturwissenschaften 1993, 80, 397.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 521
  • 4
    • 0027423025 scopus 로고
    • For example see: Wong, C.-H.; Halcomb, R. L.; Ichikawa, Y.; Kajimoto; T. Angew. Chem. 1995, 107, 569; Angew. Chem., Int. Ed. Engl. 1995, 34, 521. Legler, G. Naturwissenschaften 1993, 80, 397.
    • (1993) Naturwissenschaften , vol.80 , pp. 397
    • Legler, G.1
  • 9
    • 0001485244 scopus 로고
    • For recent reviews about applications of ring closing olefin metathesis see: Schmalz, H.-G. Angew. Chem. 1995, 107, 1981; Angew. Chem., Int. Ed. Engl. 1995, 34, 1833. Koert, U. Nach. Chem. Tech. Lab. 1995, 43, 809.
    • (1995) Angew. Chem. , vol.107 , pp. 1981
    • Schmalz, H.-G.1
  • 10
    • 33750239613 scopus 로고
    • For recent reviews about applications of ring closing olefin metathesis see: Schmalz, H.-G. Angew. Chem. 1995, 107, 1981; Angew. Chem., Int. Ed. Engl. 1995, 34, 1833. Koert, U. Nach. Chem. Tech. Lab. 1995, 43, 809.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 1833
  • 11
    • 0001264772 scopus 로고
    • For recent reviews about applications of ring closing olefin metathesis see: Schmalz, H.-G. Angew. Chem. 1995, 107, 1981; Angew. Chem., Int. Ed. Engl. 1995, 34, 1833. Koert, U. Nach. Chem. Tech. Lab. 1995, 43, 809.
    • (1995) Nach. Chem. Tech. Lab. , vol.43 , pp. 809
    • Koert, U.1
  • 17
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    • note
    • The yields for the dihydroxylation and epoxidation steps given in Scheme 2 refer to isolated, purified main products, which were used for the next steps (see experimental). No attempts were made to determine the exact selectivities of these standard steps.
  • 23
    • 33746236970 scopus 로고
    • Schwab, P.; France, M. B.; Ziller, J. W.; Grubbs, R. H. Angew. Chem. 1995, 107, 2179; Angew. Chem., Int. Ed. Engl. 1995, 34, 2039.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 2039
  • 24
    • 85085844515 scopus 로고    scopus 로고
    • note
    • 3CH = CH).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.