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Volumn 75, Issue 1, 2010, Pages 11-15

Two-step synthesis of aza- and diazaindoles from chloroamino-N-heterocycles using ethoxyvinylborolane

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL EQUATIONS; N-HETEROCYCLES; PROTECTING GROUP; SUZUKI-MIYAURA COUPLING; TWO-STEP SYNTHESIS;

EID: 73449127236     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo902143f     Document Type: Article
Times cited : (60)

References (45)
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    • For selected recent examples of kinase inhibitors, see: a, Patent Application WO2008157179
    • For selected recent examples of kinase inhibitors, see: (a) Dyke, H. J.; Price, S.; Williams, K. Patent Application WO2008157179, 2008.
    • (2008)
    • Dyke, H.J.1    Price, S.2    Williams, K.3
  • 4
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    • Tsai, J.; Lee, J. T.; Wang, W.; Zhang, J.; Cho, H.; Mamo, S.; Bremer, R.; Gillette, S.; Kong, J.; Haass, N. K.; Sproesser, K.; Li, L.; Smalley, K. S. M.; Fong, D.; Zhu, Y.-L.; Marimuthu, A.; Nguyen, H.; Lam, B.; Liu, J.; Cheung, I.; Rice, J.; Suzuki, Y.; Luu, C.; Settachatgul, C.; Shellooe, R.; Cantwell, J.; Kim, S.-H.; Schlessinger, J.; Zhang, K. Y. J.; West, B. L.; Powell, B.; Habets, G.; Zhang, C.; Ibrahim, P. N.; Hirth, P.; Artis, D. R.; Herlyn, M.; Bollag, G. Proc. Natl. Acad. Sci. U.S.A. 2008, 105, 3041.
    • (d) Tsai, J.; Lee, J. T.; Wang, W.; Zhang, J.; Cho, H.; Mamo, S.; Bremer, R.; Gillette, S.; Kong, J.; Haass, N. K.; Sproesser, K.; Li, L.; Smalley, K. S. M.; Fong, D.; Zhu, Y.-L.; Marimuthu, A.; Nguyen, H.; Lam, B.; Liu, J.; Cheung, I.; Rice, J.; Suzuki, Y.; Luu, C.; Settachatgul, C.; Shellooe, R.; Cantwell, J.; Kim, S.-H.; Schlessinger, J.; Zhang, K. Y. J.; West, B. L.; Powell, B.; Habets, G.; Zhang, C.; Ibrahim, P. N.; Hirth, P.; Artis, D. R.; Herlyn, M.; Bollag, G. Proc. Natl. Acad. Sci. U.S.A. 2008, 105, 3041.
  • 7
    • 73449116263 scopus 로고    scopus 로고
    • For recent examples of nonkinase inhibitors, see: a, Patent Application WO 2008003736
    • For recent examples of nonkinase inhibitors, see: (a) Stoit, A.; Coolen, H. K. A. C.; Van Der Neut, M. A. W.; Kruse, C. G. Patent Application WO 2008003736, 2008.
    • (2008)
    • Stoit, A.1    Coolen, H.K.A.C.2    Van Der Neut, M.A.W.3    Kruse, C.G.4
  • 15
    • 48649100604 scopus 로고    scopus 로고
    • Numerous examples exist in the literature. In this one, substituents in the 2-position decrease the activity of the azaindole inhibitor: Tang, J.; Hamajima, T.; Nakano, M.; Sato, H.; Dickerson, S. H.; Lackey, K. E. Bioorg. Med. Chem. Lett. 2008, 18, 4610.
    • Numerous examples exist in the literature. In this one, substituents in the 2-position decrease the activity of the azaindole inhibitor: Tang, J.; Hamajima, T.; Nakano, M.; Sato, H.; Dickerson, S. H.; Lackey, K. E. Bioorg. Med. Chem. Lett. 2008, 18, 4610.
  • 29
    • 73449085362 scopus 로고    scopus 로고
    • Patent ApplicationWO2005/107760, 2005
    • (c) Hong, J.; Gray, N. S.; Schultz, P. Patent ApplicationWO2005/107760, 2005.
    • Hong, J.1    Gray, N.S.2    Schultz, P.3
  • 34
    • 73449148907 scopus 로고    scopus 로고
    • (Z-isomer): Apollo Scientific Ltd. (http://www.apolloscientific.co. uk) and Synthonix Corporation (http://www.synthonix.com).
    • (Z-isomer): Apollo Scientific Ltd. (http://www.apolloscientific.co. uk) and Synthonix Corporation (http://www.synthonix.com).
  • 45
    • 0024599583 scopus 로고    scopus 로고
    • Acetylene 12 was synthesized according to Pons, J.-M.; Kocieski, P. Tetrahedron Lett. 1989, 30, 1833, but DMPU was substituted for highly toxic HMPA.
    • Acetylene 12 was synthesized according to Pons, J.-M.; Kocieski, P. Tetrahedron Lett. 1989, 30, 1833, but DMPU was substituted for highly toxic HMPA.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.