메뉴 건너뛰기




Volumn 3, Issue 9, 2014, Pages 926-931

Aza-[4+3] and aza-[3+2] annulations for synthesis of dihydroazepines and dihydropyrroles from alkynes, sulfonyl azides, and 1,3-dienes

Author keywords

[No Author keywords available]

Indexed keywords


EID: 84909952294     PISSN: 21935807     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajoc.201402071     Document Type: Article
Times cited : (44)

References (58)
  • 45
    • 84901617584 scopus 로고    scopus 로고
    • A paper reporting an essentially same reaction recently appeared, Angew. Chem. 2014, 126, 5768
    • A paper reporting an essentially same reaction recently appeared: H. Shang, Y. Wang, Y. Tian, J. Feng, Y. Tang, Angew. Chem. Int. Ed. 2014, 22, 5662; Angew. Chem. 2014, 126, 5768.
    • (2014) Angew. Chem. Int. Ed. , vol.22 , pp. 5662
    • Shang, H.1    Wang, Y.2    Tian, Y.3    Feng, J.4    Tang, Y.5
  • 50
    • 84909966970 scopus 로고    scopus 로고
    • The reactions of 2a (E only) and 2a' (E/Z=1:1.27) gave the same racemic mixture of 4a (Chiralpak 1B-3 using EtOH/n-hexane=1:4 as the eluent was used in chiral-phase HPLC analysis)
    • The reactions of 2a (E only) and 2a' (E/Z=1:1.27) gave the same racemic mixture of 4a (Chiralpak 1B-3 using EtOH/n-hexane=1:4 as the eluent was used in chiral-phase HPLC analysis).
  • 56
    • 84871977552 scopus 로고    scopus 로고
    • 4-n-Butyl triazole was converted into 4-n-butyl dihydroazepine in 25% yield. the reaction of 4-tert-butyl-1-mesyl-1,2,3-triazole gave an a,b-unsaturated N-mesyl imine in quantitative yield via rearrangement of methyl group, Angew. Chem. 2012, 124, 13231
    • 4-n-Butyl triazole was converted into 4-n-butyl dihydroazepine in 25% yield. the reaction of 4-tert-butyl-1-mesyl-1,2,3-triazole gave an a,b-unsaturated N-mesyl imine in quantitative yield via rearrangement of methyl group. N. Selander, B. T. Worrell, V. V. Fokin, Angew. Chem. Int. Ed. 2012, 51, 13054; Angew. Chem. 2012, 124, 13231.
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 13054
    • Selander, N.1    Worrell, B.T.2    Fokin, V.V.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.