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Volumn , Issue 11, 2005, Pages 1751-1756

Diastereo- and enantioselective synthesis of 2-substituted 1-aminocyclopropane-1-carboxylic acids. Application to the synthesis of protected 2,3-methano analogs of ornithine and glutamic acid

Author keywords

Amino acids; Asymmetric synthesis; Chemoselectivity; Chiral pool; Cyclopropanes; Protecting groups

Indexed keywords

CARBON; HYDROGEN BONDS; PROPANE; STEREOCHEMISTRY; SUBSTITUTION REACTIONS;

EID: 23044511485     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-870007     Document Type: Article
Times cited : (7)

References (52)
  • 27
    • 0027997482 scopus 로고
    • Chang, H. S.; Bergmeier, S. C.; Frick, J. A.; Bathe, A.; Rapoport, H. J. Org. Chem. 1994, 59, 5336, it provides the first example of a highly efficacious use of the pendant γ-hydroxyethyl group on a cyclopropane for further functional elaboration. The use of a similarly substituted cyclopropane was reported recently in reference 7a.
    • (1994) J. Org. Chem. , vol.59 , pp. 5336
    • Chang, H.S.1    Bergmeier, S.C.2    Frick, J.A.3    Bathe, A.4    Rapoport, H.5
  • 34
    • 0011166757 scopus 로고
    • Wiley: New York
    • A general procedure for using ethyl chloroformate as an activating agent in a Curtius reaction is described in: Kaiser, C.; Weinstock, J. Org. Synth. Coll. Vol. VI; Wiley: New York, 1988, 910.
    • (1988) J. Org. Synth. Coll. Vol. VI , vol.6 , pp. 910
    • Kaiser, C.1    Weinstock2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.