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Volumn 54, Issue 30, 2013, Pages 3974-3976

Furan ring opening-pyrrole ring closure. A simple route to 1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-3-ones

Author keywords

1,2,3,4 Tetrahydropyrrolo 1,2 a pyrazines; Furans; Recyclization; Ring closure; Ring opening

Indexed keywords

1,2,3,4 TETRAHYDROPYRROLO[1,2 A]PYRAZIN 3 ONE; FURAN; PYRROLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84879409866     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2013.05.066     Document Type: Article
Times cited : (19)

References (45)
  • 38
    • 84875712000 scopus 로고    scopus 로고
    • When this manuscript was in preparation, Batra and co-workers reported the analogous preparation of 1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazines from furfurylamines and optically active α-amino acids, see: S. Bhowmik, A.K.S. Kumar, and S. Batra Tetrahedron Lett. 54 2013 2251 2254
    • (2013) Tetrahedron Lett. , vol.54 , pp. 2251-2254
    • Bhowmik, S.1    Kumar, A.K.S.2    Batra, S.3
  • 44
    • 0025975362 scopus 로고
    • Furfurylamine 3a is commercially available. Furfurylamines 3b-g were synthesized from the corresponding oximes by the published method: Y.-H. Kuo, and K.-S. Shih Chem. Pharm. Bull. 39 1991 181 183
    • (1991) Chem. Pharm. Bull. , vol.39 , pp. 181-183
    • Kuo, Y.-H.1    Shih, K.-S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.