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Volumn 67, Issue 38, 2011, Pages 7330-7335

Synthesis of 1,6-dihydropyrrolo[2,3-g]indazoles using Larock indole annulation

Author keywords

Indazole; Larock indole annulation; Pyrroloindazole; Regioselectivity

Indexed keywords

1,6 DIHYDROPYRROLO[2,3 G]INDAZOLE DERIVATIVE; 4 IODO 6 NITRO 1 (TETRAHYDRO 2H PYRAN 2 YL) 1H INDAZOL 5 AMINE; 5 NITRO 1 (TETRAHYDRO 2H PYRAN 2 YL) 1H INDAZOL 6 AMINE; 5 NITRO 1 (TETRAHYDRO 2H PYRAN 2 YL) 7 (2 TRIMETHYLSILYLETHYNYL) 1H INDAZOL 6 AMINE; 5 NITRO 1 (TETRAHYDRO 2H PYRAN 2 YL) 7 (TRIMETHYLSILYL) 1,6 DIHYDROPYRROLO[2,3 G]INDAZOLE; 5 NITRO 8 PHENYL 1 (TETRAHYDRO 2H PYRAN 2 YL) 1,6 DIHYDROPYRROLO[2,3 G]INDAZOLE; 5 NITRO 8 PHENYL 1,6 DIHYDROPYRROLO[2,3 G]INDAZOLE; 5 NITRO 8 PROPYL 1 (TETRAHYDRO 2H PYRAN 2 YL) 1,6 DIHYDROPYRROLO[2,3 G]INDAZOLE; 5 NITRO 8 PROPYL 1,6 DIHYDROPYRROLO[2,3 G]INDAZOLE; 6 NITRO 1 (TETRAHYDRO 2H PYRAN 2 YL) 1H INDAZOL 6 AMINE; 7 ETHYL 5 NITRO 8 PHENYL 1 (TETRAHYDRO 2H PYRAN 2 YL) 1,6 DIHYDROPYRROLO[2,3 G]INDAZOLE; 7 IODO 5 NITRO 1 (TETRAHYDRO 2H PYRAN 2 YL) 1H INDAZOL 6 AMINE; 8 DIETHOXYMETHYL 5 NITRO 1 (TETRAHYDRO 2H PYRAN 2 YL) 1,6 DIHYDROPYRROLO[2,3 G]INDAZOLE; 8 ETHYL 5 NITRO 7 PHENYL 1 (TETRAHYDRO 2H PYRAN 2 YL) 1,6 DIHYDROPYRROLO[2,3 G]INDAZOLE; ALKYNE; ETHYL 5 NITRO 8 PHENYL 1 (TETRAHYDRO 2H PYRAN 2 YL) 1,6 DIHYDROPYRROLO[2,3 G]INDAZOLE 7 CARBOXYLATE; ETHYL 8 METHYL 5 NITRO 1 (TETRAHYDRO 2H PYRAN 2 YL) 1,6 DIHYDROPYRROLO[2,3 G]INDAZOLE 7 CARBOXYLATE; INDAZOLE DERIVATIVE; METHYL 5 NITRO 8 PROPYL 1 (TETRAHYDRO 2H PYRAN 2 YL) 1,6 DIHYDROPYRROLO[2,3 G]INDAZOLE 7 CARBOXYLATE; UNCLASSIFIED DRUG;

EID: 80051785112     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2011.07.029     Document Type: Article
Times cited : (23)

References (53)
  • 4
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    • For recent examples of the Larock indole synthesis, see
    • For recent examples of the Larock indole synthesis, see
  • 14
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    • For a recent example using Cacchi's strategy for indole synthesis, see: Y. Chen, N.A. Markina, and R.C. Larock Tetrahedron 65 2009 8908
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    • For recent examples, see
    • For recent examples, see
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    • For review on indazoles, see
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    • 1H NOESY experiments
    • 1H NOESY experiments.
  • 47
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    • 6), major regioisomer: 6.66 (1H, d, J=8.5 Hz), 7.52 (1H, s), 8.43 (1H, s), 8.66 (1H, s), 12.05 (1H, br s); minor regioisomer: 6.01 (1H, d, J=9 Hz), 6.94 (1H, s), 8.35 (1H, s), 8.59 (1H, s), 11.85 (1H, br s). Compounds 19 and 20 (400 MHz, CDCl3), major regioisomer: 5.95 (1H, d, J=8.5 Hz), 8.20 (1H, s); minor regioisomer: 6.21 (1H, d, J=8.5 Hz), 8.29 (1H, s).
    • 6), major regioisomer: 6.66 (1H, d, J=8.5 Hz), 7.52 (1H, s), 8.43 (1H, s), 8.66 (1H, s), 12.05 (1H, br s); minor regioisomer: 6.01 (1H, d, J=9 Hz), 6.94 (1H, s), 8.35 (1H, s), 8.59 (1H, s), 11.85 (1H, br s). Compounds 19 and 20 (400 MHz, CDCl3), major regioisomer: 5.95 (1H, d, J=8.5 Hz), 8.20 (1H, s); minor regioisomer: 6.21 (1H, d, J=8.5 Hz), 8.29 (1H, s).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.