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Volumn 67, Issue 49, 2011, Pages 9522-9528

An efficient one-pot multicomponent approach to 5-amino-7-aryl-8- nitrothiazolo[3,2-a]pyridines

Author keywords

Heterocycles; Knoevenagel reaction; Multicomponent reactions; Nitrile; Pyridine; Thiazoline

Indexed keywords

2 NITROMETHYLENETHIAZOLIDINE; 2 PHENYLSULFONYLACETONITRILE; 5 AMINO 7 (2 BROMOPHENYL) 8 NITRO 3,7 DIHYDRO 2H THIAZOLO [3,2 ALPHA]PYRIDINE 6 CARBONITRILE; 5 AMINO 7 (2 FLUOROPHENYL) 8 NITRO 3,7 DIHYDRO 2H THIAZOLO [3,2 ALPHA]PYRIDINE 6 CARBONITRILE; 5 AMINO 7 (2,4 DICHLOROPHENYL) 8 NITRO 3,7 DIHYDRO 2H THIAZOLO [3,2 ALPHA]PYRIDINE 6 CARBONITRILE; 5 AMINO 7 (2,6 DICHLOROPHENYL) 8 NITRO 3,7 DIHYDRO 2H THIAZOLO[3,2 ALPHA]PYRIDINE 6 CARBONITRILE; 5 AMINO 7 (4 (DIMETHYLAMINO)PHENYL) 8 NITRO 3,7 DIHYDRO 2H THIAZOLO [3,2 ALPHA]PYRIDINE 6 CARBONITRILE; 5 AMINO 7 (4 BROMOPHENYL) 8 NITRO 3,7 DIHYDRO 2H THIAZOLO [3,2 ALPHA]PYRIDINE 6 CARBONITRILE; 5 AMINO 7 (4 CHLOROPHENYL) 8 NITRO 3,7 DIHYDRO 2H THIAZOLO [3,2 ALPHA]PYRIDINE 6 CARBONITRILE; 5 AMINO 7 (4 FLUOROPHENYL) 8 NITRO 3,7 DIHYDRO 2H THIAZOLO [3,2 ALPHA]PYRIDINE 6 CARBONITRILE; 5 AMINO 7 (5 BROMO 2 HYDROXYPHENYL) 8 NITRO 3,7 DIHYDRO 2H THIAZOLO [3,2 ALPHA]PYRIDINE 6 CARBONITRILE; 5 AMINO 7 ARYL 8 NITROTHIAZOLO[3,2 ALPHA]PYRIDINE DERIVATIVE; 5 AMINO 8 NITRO 7 (4 NITROPHENYL) 3,7 DIHYDRO 2H THIAZOLO [3,2 ALPHA]PYRIDINE 6 CARBONITRILE; 5 AMINO 8 NITRO 7 PHENYL 3,7 DIHYDRO 2H THIAZOLO [3,2 ALPHA]PYRIDINE 6 CARBONITRILE; 7 (4 CHLOROPHENYL) 8 NITRO 6 (PHENYLSULFONYL) 3,7 DIHYDRO 2H THIAZOLO [3,2 ALPHA]PYRIDIN 5 AMINE; 7 (4 FLUOROPHENYL) 8 NITRO 6 (PHENYLSULFONYL) 3,7 DIHYDRO 2H THIAZOLO [3,2 ALPHA]PYRIDIN 5 AMINE; 7 (4 FLUOROPHENYL) 8 NITRO 6 (PHENYLSULFONYL) 6,7 DIHYDRO 2H THIAZOLO [3,2 ALPHA]PYRIDIN 5(3H) IMINE; 8 NITRO 7 PHENYL 6 (PHENYLSULFONYL) 3,7 DIHYDRO 2H THIAZOLO [3,2 ALPHA]PYRIDIN 5 AMINE; 8 NITRO 7 PHENYL 6 (PHENYLSULFONYL) 6,7 DIHYDRO 2H THIAZOLO [3,2 ALPHA]PYRIDIN 5(3H) IMINE; ALDEHYDE; CARBENE; ETHYL 2 CYANOACETATE; ETHYL 5 AMINO 7 (4 BROMOPHENYL) 8 NITRO 3,7 DIHYDRO 2H THIAZOLO [3,2 ALPHA]PYRIDINE 6 CARBOXYLATE; ETHYL 5 AMINO 7 (4 CHLOROPHENYL) 8 NITRO 3,7 DIHYDRO 2H THIAZOLO [3,2 ALPHA]PYRIDINE 6 CARBOXYLATE; ETHYL 5 AMINO 8 NITRO 7 (4 NITROPHENYL)D3,7DDIHYDRO 2H THIAZOLO [3,2 ALPHA]PYRIDINE 6 CARBOXYLATE; MALONONITRILE; NITRILE; PYRIDINE DERIVATIVE; THIAZOLE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 80555122767     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2011.10.005     Document Type: Article
Times cited : (50)

References (20)
  • 17
    • 0021686418 scopus 로고
    • The double-bond geometry in 2-nitromethylenethiazoline (1) is solvent-dependent, with the expected preference for hydrogen bonding with the thiazoline NH being over-ridden in some instances by an attractive interaction with the sulfur. For leading references see
    • The double-bond geometry in 2-nitromethylenethiazoline (1) is solvent-dependent, with the expected preference for hydrogen bonding with the thiazoline NH being over-ridden in some instances by an attractive interaction with the sulfur. For leading references see S. Rajappa, K. Nagarajan, K. Venkatesan, N. Kamath, V.M. Padmanabhan, W. Von Philipsborn, B.C. Chen, and R. Mueller Helv. Chim. Acta 67 1984 1669 1680
    • (1984) Helv. Chim. Acta , vol.67 , pp. 1669-1680
    • Rajappa, S.1    Nagarajan, K.2    Venkatesan, K.3    Kamath, N.4    Padmanabhan, V.M.5    Von Philipsborn, W.6    Chen, B.C.7    Mueller, R.8
  • 18
    • 0024802255 scopus 로고
    • Throughout this manuscript, the structure has been represented with ambiguous stereochemistry since this was not explicitly investigated
    • S. Rajappa, B.M. Bhawal, A.R.A.S. Deshmukh, S.G. Manjunatha, and J. Chandrasekhar J. Chem. Soc., Chem. Commun. 1989 1729 1730 Throughout this manuscript, the structure has been represented with ambiguous stereochemistry since this was not explicitly investigated
    • (1989) J. Chem. Soc., Chem. Commun. , pp. 1729-1730
    • Rajappa, S.1    Bhawal, B.M.2    Deshmukh, A.R.A.S.3    Manjunatha, S.G.4    Chandrasekhar, J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.