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Volumn 4, Issue 8, 2014, Pages 3758-3767

One-pot four-component approach for the construction of dihydropyridines and dihydropyridinones using amines and activated alkynes

Author keywords

[No Author keywords available]

Indexed keywords

ACID TREATMENTS; ACTIVATED ALKYNES; DIASTEREOMERS; DIHYDROPYRIDINES; DIPOLAR ADDITIONS; DOMINO REACTIONS; SELECTIVE FORMATION; SOLVENT FREE CONDITIONS;

EID: 84890815077     PISSN: None     EISSN: 20462069     Source Type: Journal    
DOI: 10.1039/c3ra45850d     Document Type: Article
Times cited : (20)

References (76)
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    • 0004101860 scopus 로고
    • in, ed. A. Padwa, Wiley-Interscience, New York, 1-176
    • R. Huisgen, in 1,3-Dipolar Cycloaddition Chemistry, ed., A. Padwa, Wiley-Interscience, New York, 1984, vol. 1, pp. 1-176
    • (1984) 1,3-Dipolar Cycloaddition Chemistry , vol.1
    • Huisgen, R.1
  • 75
    • 84861529538 scopus 로고    scopus 로고
    • All the reactions performed during the optimization of acid catalysts for the transformation of 1 mmol of dihydropyridine 5a to dihydropyridinone 13a were carried out using 1-2 mL of the acid catalyst Crystallographic data for compound 13d
    • S. E. Kiruthika R. Amritha P. T. Perumal Tetrahedron Lett. 2012 53 3268
    • (2012) Tetrahedron Lett. , vol.53 , pp. 3268
    • Kiruthika, S.E.1    Amritha, R.2    Perumal, P.T.3
  • 76
    • 84856692224 scopus 로고    scopus 로고
    • 13C NMR spectrum could be masking one of the acyclic carbons. Thus one of the signals was missing (tentatively corresponding to the C-3 carbon). Otherwise the compounds are characterized completely through other methods along with the support of the X-ray single crystal analysis performed for the representative compound 13d
    • T. Sengupta K. S. Gayen P. Pandit D. K. Maiti Chem.-Eur. J. 2012 18 1905
    • (2012) Chem.-Eur. J. , vol.18 , pp. 1905
    • Sengupta, T.1    Gayen, K.S.2    Pandit, P.3    Maiti, D.K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.