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Volumn , Issue 2, 2005, Pages 319-321

Enantioselective synthesis of [(1R,3-exo)-2-benzyl-2-azabicyclo[2.2.1]hept- 5-en-3-yl]methanol via Aza-Diels-Alder reaction

Author keywords

Asymmetric synthesis; Chiral auxiliaries; Diels Alder reactions; Induction

Indexed keywords

2 BENZYL 2 AZABICYCLO[2.2.1]HEPT 5 EN 3 YL]METHANOL; METHANOL; UNCLASSIFIED DRUG;

EID: 13844274936     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2004-836068     Document Type: Article
Times cited : (20)

References (20)
  • 16
    • 13844286301 scopus 로고    scopus 로고
    • note
    • 4. Removal of the solvent on a rotary evaporator yielded an orange oil (2.3 g) which was purified by column chromatography (silica gel) using hexane-EtOAc 3:1 as eluent. Fractions 7-10 afforded a colorless oil (1.61 g) identified as the pure major adduct (1R3-exo) 1a. Yield 70%.
  • 17
    • 13844300381 scopus 로고    scopus 로고
    • note
    • 2: 443.2824. Found: 443.2817.
  • 18
    • 13844303947 scopus 로고    scopus 로고
    • note
    • 2: 443.2824. Found: 443.2814.
  • 19
    • 13844259613 scopus 로고    scopus 로고
    • note
    • 17NO: 215.1310. Found: 215.1319.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.