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Volumn , Issue 18, 2010, Pages 3152-3162

Novel syntheses of variably substituted pyrrolo[2,3-d]thiazoles

Author keywords

heterocycles; microwave irradiation; pyrroles; thiazoles

Indexed keywords

HECK CYCLIZATION; HETEROCYCLES; MICROWAVE ASSISTED; PYRROLES; SUZUKI REACTION; THIAZOLES;

EID: 77956494237     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1258159     Document Type: Article
Times cited : (4)

References (28)
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    • For a review of pyrrolo[2,1-b ]thiazoles, see
    • For a review of pyrrolo[2,1-b ]thiazoles, see:, Tverdokhlebov A V., Heterocycles 2007 71 761
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    • US Patent Appl. US 20020058216; Chem. Abstr. 2002, 136, 393179
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    • Nakamura, T.1    Hioki, T.2    Ohzeki, K.3    Hanaki, N.4
  • 5
    • 0000617337 scopus 로고
    • For the original synthesis of pyrrolo[3,2-d ]thiazoles, see
    • For the original synthesis of pyrrolo[3,2-d ]thiazoles, see:, Shafiee A, Mazloumi A, Cohen V I., J. Heterocycl. Chem. 1979 16 1563
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    • Shafiee, A.1    Mazloumi, A.2    Cohen, V.I.3
  • 16
    • 2442455607 scopus 로고    scopus 로고
    • For an explicit example of a Boc-protected iodoaniline being cyclized to the corresponding indole after Sonogashira coupling employing TBAF as base in a one-pot procedure, see
    • For an explicit example of a Boc-protected iodoaniline being cyclized to the corresponding indole after Sonogashira coupling employing TBAF as base in a one-pot procedure, see:, Suzuki N, Yasaki S, Yasuhara A, Sakamoto T, Chem. Pharm. Bull. 2003 51 1170
    • (2003) Chem. Pharm. Bull. , vol.51 , pp. 1170
    • Suzuki, N.1    Yasaki, S.2    Yasuhara, A.3    Sakamoto, T.4
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    • For a discussion of aminopalladation/reductive elimination reactions for the syntheses of indoles, see
    • For a discussion of aminopalladation/reductive elimination reactions for the syntheses of indoles, see:, Arcadi A, Cacchi S, Marinelli F, Tetrahedron Lett. 1992 33 3915
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    • Arcadi, A.1    Cacchi, S.2    Marinelli, F.3
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    • 0347096620 scopus 로고
    • The yields of 4-and 5-aminothiazoles are low and rapid decomposition to a black solid is particularly mentioned for the 4-aminothiazole, see
    • The yields of 4-and 5-aminothiazoles are low and rapid decomposition to a black solid is particularly mentioned for the 4-aminothiazole, see:, Diener H, Zollinger H, Can. J. Chem. 1986 64 1102
    • (1986) Can. J. Chem. , vol.64 , pp. 1102
    • Diener, H.1    Zollinger, H.2
  • 25
    • 0034679471 scopus 로고    scopus 로고
    • Knochel and co-workers mention the importance of NMP as solvent in combination with t-BuOK to induce cyclization to the pyrrole moiety:; Angew. Chem. 2000, 112, 2607
    • Knochel and co-workers mention the importance of NMP as solvent in combination with t-BuOK to induce cyclization to the pyrrole moiety:, Rodriguez A L., Koradin C, Dohle W, Knochel P, Angew. Chem. Int. Ed. 2000 39 2488; Angew. Chem. 2000, 112, 2607
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  • 26
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    • Pyrrolo[3,2-d ]thiazole as a keratin dyeing compound is claimed, but its synthesis is not explicitly stated, see: PCT Int. Appl. WO 2005077324; Chem. Abstr. 2005, 143, 234964
    • Pyrrolo[3,2-d ]thiazole as a keratin dyeing compound is claimed, but its synthesis is not explicitly stated, see:, Murphy B P., Glenn R W. Jr., Lim M I., Gardlik J M., Jones S D., Laidig W D., Shaffer J D., PCT Int. Appl. WO 2005077324 2005; Chem. Abstr. 2005, 143, 234964
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    • Murphy, B.P.1    Glenn, Jr.R.W.2    Lim, M.I.3    Gardlik, J.M.4    Jones, S.D.5    Laidig, W.D.6    Shaffer, J.D.7
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    • The formation of a black slurry residue is observed, probably due to polymerization.
    • The formation of a black slurry residue is observed, probably due to polymerization.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.