메뉴 건너뛰기




Volumn 5, Issue , 2009, Pages

Zeolite catalyzed solvent-free one-pot synthesis of dihydropyrimidin-2(1H)- ones - A practical synthesis of monastrol

Author keywords

Biginelli reaction; DHPMs; MCR; Neat; Zeolite

Indexed keywords


EID: 76249099753     PISSN: 18605397     EISSN: 18605397     Source Type: Journal    
DOI: 10.3762/bjoc.5.4     Document Type: Article
Times cited : (25)

References (17)
  • 2
    • 0034518876 scopus 로고    scopus 로고
    • Recent advances in the Biginelli dihydropyrimidine synthesis. New tricks from an old dog
    • DOI 10.1021/ar000048h
    • Kappe, C. O. Acc. Chem. Res. 2000, 33, 879-888. doi:10.1021/ar000048h. (Pubitemid 32056773)
    • (2000) Accounts of Chemical Research , vol.33 , Issue.12 , pp. 879-888
    • Kappe, C.O.1
  • 3
    • 4644324512 scopus 로고    scopus 로고
    • Demonstration of the feasibility of a direct solid-phase split-pool Biginelli synthesis of 3,4-dihydropyrimidinones
    • DOI 10.1021/ol048946r
    • Lusch, M. J.; Tallarico, J. A. Org. Lett. 2004, 6, 3237-3240. doi:10.1021/ol048946r. (Pubitemid 39297308)
    • (2004) Organic Letters , vol.6 , Issue.19 , pp. 3237-3240
    • Lusch, M.J.1    Tallarico, J.A.2
  • 4
  • 6
    • 0038203081 scopus 로고    scopus 로고
    • The first catalytic, asymmetric -additions of isocyanides. Lewis-base-catalyzed, enantioselective Passerini-type reactions
    • DOI 10.1021/ja035410c
    • Denmark, S. E.; Fan, Y. J. Am. Chem. Soc. 2003, 125, 7825-7827. doi:10.1021/ja035410c. (Pubitemid 36782158)
    • (2003) Journal of the American Chemical Society , vol.125 , Issue.26 , pp. 7825-7827
    • Denmark, S.E.1    Fan, Y.2
  • 8
    • 20644448209 scopus 로고    scopus 로고
    • Highly enantioselective one-pot, three-component imino-reformatsky reaction
    • DOI 10.1002/anie.200462757
    • Cozzi, P. G.; Rivalta, E. Angew. Chem., Int. Ed. 2005, 44, 3600-3603. doi:10.1002/anie.200462757. (Pubitemid 40831824)
    • (2005) Angewandte Chemie - International Edition , vol.44 , Issue.23 , pp. 3600-3603
    • Cozzi, P.G.1    Rivalta, E.2
  • 12
    • 0034519777 scopus 로고    scopus 로고
    • Biologically active dihydropyrimidones of the Biginelli-type - A literature survey
    • DOI 10.1016/S0223-5234(00)01189-2
    • Kappe, C. O. Eur. J. Med. Chem. 2000, 35, 1043-1052. doi:10.1016/S0223- 5234(00)01189-2. (Pubitemid 32050011)
    • (2000) European Journal of Medicinal Chemistry , vol.35 , Issue.12 , pp. 1043-1052
    • Kappe, C.O.1
  • 13
    • 0042469059 scopus 로고    scopus 로고
    • doi:10.1002/qsar.200320001
    • Kappe, C. O. QSAR Comb. Sci. 2003, 22, 630-645. doi:10.1002/qsar. 200320001.
    • (2003) QSAR Comb. Sci. , vol.22 , pp. 630-645
    • Kappe, C.O.1
  • 14
    • 0027205552 scopus 로고
    • doi:10.1016/S0040-4020(01)87971-0 For review
    • Kappe, C. O. Tetrahedron 1993, 49, 6937-6963. doi:10.1016/S0040-4020(01) 87971-0 For review.
    • (1993) Tetrahedron , vol.49 , pp. 6937-6963
    • Kappe, C.O.1
  • 15
    • 0030732273 scopus 로고    scopus 로고
    • A reexamination of the mechanism of the Biginelli dihydropyrimidine synthesis. Support for an N-acyliminium ion intermediate
    • DOI 10.1021/jo971010u
    • Kappe, C. O. J. Org. Chem. 1997, 62, 7201-7204. doi:10.1021/jo971010u. (Pubitemid 27463078)
    • (1997) Journal of Organic Chemistry , vol.62 , Issue.21 , pp. 7201-7204
    • Kappe, C.O.1
  • 17
    • 0032524801 scopus 로고    scopus 로고
    • Unprecedented catalytic three component one-pot condensation reaction: An efficient synthesis of 5-alkoxycarbonyl-4-aryl-3,4-dihydropyrimidin- 2(1H)-ones
    • DOI 10.1021/jo970846u
    • Hu, E. H.; Sidler, D. R.; Dolling, U.-H. J. Org. Chem. 1998, 63, 3454-3457. doi:10.1021/jo970846u. (Pubitemid 28269630)
    • (1998) Journal of Organic Chemistry , vol.63 , Issue.10 , pp. 3454-3457
    • Hu, E.H.1    Sidler, D.R.2    Dolling, U.-H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.