메뉴 건너뛰기




Volumn 51, Issue 6, 2010, Pages 903-906

Polycyclic N-heterocyclic compounds. Part 61: A novel Truce-Smiles type rearrangement reaction of 4-(2-cyanovinyloxy)butanenitriles to give cycloalkeno[1,2-d]furo[2,3-b]pyridines

Author keywords

Cyanovinyl ether; Cycloalkeno 1,2 d furo 2,3 b pyridine; Estervinyl ether; Heterocycle; Michael addition; Truce Smiles rearrangement

Indexed keywords

4 (2 CYANOVINYLOXY)BUTANENITRILE DERIVATIVE; CYCLOALKENO[1,2 D]FURO[2,3 B]PYRIDINE DERIVATIVE; LACTAM; NITRILE; PYRIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 73249146107     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.12.010     Document Type: Article
Times cited : (18)

References (15)
  • 2
    • 54449097480 scopus 로고    scopus 로고
    • For a leading review, see
    • For a leading review, see. Snape T.J. Chem. Soc. Rev. 37 (2008) 2452-2458
    • (2008) Chem. Soc. Rev. , vol.37 , pp. 2452-2458
    • Snape, T.J.1
  • 3
    • 0343496824 scopus 로고    scopus 로고
    • For recent reports on Truce-Smiles rearrangement, see:
    • For recent reports on Truce-Smiles rearrangement, see:. Erickson W.R., and McKennon M.J. Tetrahedron Lett. 41 (2000) 4541-4544
    • (2000) Tetrahedron Lett. , vol.41 , pp. 4541-4544
    • Erickson, W.R.1    McKennon, M.J.2
  • 14
    • 73249115053 scopus 로고    scopus 로고
    • note
    • 3 in DMF, using strong bases directly. But the yield was relatively low (∼20%). In this case, intramolecular Claisen type condensation products were not isolated either.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.