메뉴 건너뛰기




Volumn 33, Issue 12, 2000, Pages 879-888

Recent advances in the Biginelli dihydropyrimidine synthesis. New tricks from an old dog

Author keywords

[No Author keywords available]

Indexed keywords

3,4 DIHYDROPYRIMIDIN 2(1H) ONE; ACETOACETIC ACID DERIVATIVE; ACETOACETIC ACID ETHYL ESTER; ALDEHYDE; BIOLOGICAL FACTOR; NATURAL PRODUCT; PYRIMIDINE DERIVATIVE; UNCLASSIFIED DRUG; UREA;

EID: 0034518876     PISSN: 00014842     EISSN: None     Source Type: Journal    
DOI: 10.1021/ar000048h     Document Type: Article
Times cited : (1265)

References (75)
  • 7
    • 0034678033 scopus 로고    scopus 로고
    • Target-oriented and diversity-oriented organic synthesis in drug discovery
    • (2000) Science , vol.287 , pp. 1964-1969
    • Schreiber, S.L.1
  • 11
    • 0027205552 scopus 로고
    • 100 Years of the Biginelli dihydropyrimidine synthesis
    • (1993) Tetrahedron , vol.49 , pp. 6937-6963
    • Kappe, C.O.1
  • 23
    • 0030732273 scopus 로고    scopus 로고
    • A reexamination of the mechanism of the biginelli dihydropyrimidine synthesis. Support for an N-acyliminium ion intermediate
    • (1997) J. Org. Chem. , vol.62 , pp. 7201-7204
    • Kappe, C.O.1
  • 25
    • 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
    • (1998) J. Org. Chem. , vol.63 , pp. 3454-3457
    • Hu, E.H.1    Sidler, D.R.2    Dolling, U.-H.3
  • 28
    • 26844487901 scopus 로고    scopus 로고
    • Polyphosphate ester-mediated synthesis of dihydropyrimidines. Improved conditions for the biginelli reaction
    • (1998) Synlett , pp. 718-720
    • Kappe, C.O.1    Falsone, S.F.2
  • 29
    • 0033958880 scopus 로고    scopus 로고
    • Iron(III)-catalyzed synthesis of dihydropyrimidinones. Improved conditions for the Biginelli reaction
    • (2000) Synlett , pp. 63-64
    • Lu, J.1    Ma, H.2
  • 31
    • 0034703416 scopus 로고    scopus 로고
    • Indium(III) chloride-catalyzed one-pot synthesis of dihydropyrimidinones by a three-component coupling of 1,3-dicarbonyl compounds, aldehydes, and urea: An improved procedure for the biginelli reaction
    • (2000) J. Org. Chem. , vol.65 , pp. 6270-6272
    • Ranu, B.C.1    Hajra, A.2    Jana, U.3
  • 36
    • 0032847541 scopus 로고    scopus 로고
    • Microwave-assisted high-speed parallel synthesis of 4-aryl-3,4-dihydropyrimidin-2(1H)-ones using a solventless biginelli condensation protocol
    • (1999) Synthesis , pp. 1799-1803
    • Kappe, C.O.1    Kumar, D.2    Varma, R.S.3
  • 39
    • 0001235198 scopus 로고
    • Synthesis of substituted 1,2,3,4-tetrahydro-6-methyl-2-oxo-5-pyrimidinecarboxylic acid esters: The biginelli condensation revisited
    • (1987) Heterocycles , vol.26 , pp. 1185-1188
    • O'Reilly, B.C.1    Atwal, K.S.2
  • 54
    • 0034598368 scopus 로고    scopus 로고
    • Highly versatile solid-phase synthesis of biofunctional 4-aryl-3,4-dihyropyrimidines using resin-bound isothiourea building blocks and multidirectional resin cleavage
    • (2000) Bioorg. Med. Chem. Lett. , vol.10 , pp. 49-51
    • Kappe, C.O.1
  • 65
    • 0033525676 scopus 로고    scopus 로고
    • Tuning stereoselection on tethered biginelli condensations. Synthesis of cis- or trans-1-oxo- and 1-iminohexahydropyrrolo[1,2-c]pyrimidines
    • (1999) J. Org. Chem. , vol.64 , pp. 1520-1528
    • McDonald, A.I.1    Overman, L.E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.