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Volumn 50, Issue 26, 2009, Pages 3241-3244

Tandem aza-Claisen rearrangement and ring-closing metathesis reactions: the stereoselective synthesis of functionalised carbocyclic amides

Author keywords

Aza Claisen rearrangements; Carbocyclic amides; Ring closing metathesis; Tandem reactions

Indexed keywords

ACETAMIDE DERIVATIVE; AMIDE; CYCLOHEXENYL TRICHLOROACETAMIDE; CYCLOPENTENYL TRICHLOROACETAMIDE; ETHER; METAL; UNCLASSIFIED DRUG;

EID: 65549104700     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.02.032     Document Type: Article
Times cited : (21)

References (39)
  • 1
    • 0028879573 scopus 로고
    • For general reviews on tandem reactions, see:
    • For general reviews on tandem reactions, see:. Bunce R.A. Tetrahedron 51 (1995) 13103-13159
    • (1995) Tetrahedron , vol.51 , pp. 13103-13159
    • Bunce, R.A.1
  • 20
    • 33646064214 scopus 로고    scopus 로고
    • Overman L.E. (Ed), Wiley, Hoboken, NJ and references cited therein
    • Overman L.E., and Carpenter N.E. In: Overman L.E. (Ed). Organic Reactions Vol. 66 (2005), Wiley, Hoboken, NJ 1-107 and references cited therein
    • (2005) Organic Reactions , vol.66 , pp. 1-107
    • Overman, L.E.1    Carpenter, N.E.2
  • 32
    • 65549108776 scopus 로고    scopus 로고
    • note
    • ® and washed with diethyl ether (100 mL). Concentration of the filtrate followed by flash column chromatography gave the cyclic allylic amides.
  • 39
    • 65549084788 scopus 로고    scopus 로고
    • note
    • Determination of the relative stereochemistry of the bicyclic amide 21 was accomplished using NOE experiments.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.