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Volumn 46, Issue 48, 2005, Pages 8385-8389

Meyers' bicyclic lactam formation under mild and highly stereoselective conditions

Author keywords

(R) Phenylglycinol; Meyers' bicyclic lactam; Mukaiyama's reagent; Thioester

Indexed keywords

CARBOXYLIC ACID; LACTAM DERIVATIVE; REAGENT;

EID: 27644594599     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.09.154     Document Type: Article
Times cited : (23)

References (22)
  • 12
    • 33845376014 scopus 로고
    • This alternative approach was mainly motivated by Thottathil's work which reported the condensation of (S)-5-(hydroxymethyl)2-pyrrolidinone with benzaldehyde under dehydrating conditions providing the corresponding bicyclic lactam in high yield with total diastereoselectivity. J.K. Thottatil, J.L. Moniot, R.H. Mueller, M.K.Y. Wong, and T.P. Kissick J. Org. Chem. 51 1986 3140 3143
    • (1986) J. Org. Chem. , vol.51 , pp. 3140-3143
    • Thottatil, J.K.1    Moniot, J.L.2    Mueller, R.H.3    Wong, M.K.Y.4    Kissick, T.P.5
  • 17
    • 27644535638 scopus 로고    scopus 로고
    • note
    • 2 was evaporated and the residue was purified by flash chromatography on silica gel (AcOEt/cyclohexane: 1/1) to afford trans-2d in 90% yield (de >95%).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.