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Volumn 50, Issue 49, 2009, Pages 6810-6813

Synthesis of pyrrolo[1,3]diazepines by a dipolar cycloaddition-retro-Mannich domino reaction

Author keywords

[No Author keywords available]

Indexed keywords

2,3,4,5 TETRAHYDRO 1H PYRROLO[1,2 C][1,3]DIAZEPINE; 4 THIO 3 OXAZOLIN 5 ONE DERIVATIVE; DIAZEPINE DERIVATIVE; ETHYL CYANOFORMATE; FORMIC ACID; OXAZOLONE; PYRROLO[1,3]DIAZEPINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 70350010184     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.09.107     Document Type: Article
Times cited : (12)

References (24)
  • 5
    • 0029609551 scopus 로고
    • The synthesis and biology of pyrrolo[1,3]diazepines remain essentially unexplored, in spite of some previous preparative work:
    • The synthesis and biology of pyrrolo[1,3]diazepines remain essentially unexplored, in spite of some previous preparative work:. Daich A., Ohier P., and Decroix B. J. Heterocycl. Chem. 32 (1995) 1731-1734
    • (1995) J. Heterocycl. Chem. , vol.32 , pp. 1731-1734
    • Daich, A.1    Ohier, P.2    Decroix, B.3
  • 12
    • 70350014142 scopus 로고    scopus 로고
    • Sharp, J. T., Nitrile Ylides and Nitrile imines. In Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products; Padwa, A.; Pearson, W. H.; Eds.; Chem. Heterocycl. Compds.; J. Wiley & Sons, Inc., 2002, 59, pp 473-538.
    • Sharp, J. T., Nitrile Ylides and Nitrile imines. In Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products; Padwa, A.; Pearson, W. H.; Eds.; Chem. Heterocycl. Compds.; J. Wiley & Sons, Inc., 2002, Vol. 59, pp 473-538.
  • 14
    • 4444303072 scopus 로고    scopus 로고
    • For the use of azamacrocycles in diversity-oriented synthesis, see, for example:
    • For the use of azamacrocycles in diversity-oriented synthesis, see, for example:. Wipf P., Stephenson C.R.J., and Walczak M.A.A. Org. Lett. 6 (2004) 3009-3012
    • (2004) Org. Lett. , vol.6 , pp. 3009-3012
    • Wipf, P.1    Stephenson, C.R.J.2    Walczak, M.A.A.3
  • 21
    • 61449199502 scopus 로고    scopus 로고
    • See: and references cited therein
    • See:. Jin Z. Nat. Prod. Rep. 26 (2009) 382-445 and references cited therein
    • (2009) Nat. Prod. Rep. , vol.26 , pp. 382-445
    • Jin, Z.1
  • 22
    • 70350014141 scopus 로고    scopus 로고
    • note
    • 2SNa (M+Na) 375.1143, found 375.1114.
  • 23
    • 70350040628 scopus 로고    scopus 로고
    • note
    • 4SNa (M+Na) 473.1502, found 473.1511.
  • 24
    • 70350027468 scopus 로고    scopus 로고
    • note
    • 3, 300 K) δ 7.35-7.11 (m, 10 H), 5.85 (dt, 1 H, J = 5.7, 15.5 Hz), 5.38 (dt, 1 H, J = 6.3, 15.5 Hz), 4.76 (d, 2 H, J = 5.7 Hz), 4.38 (s, 2 H), 3.86 (s, 3 H), 3.77 (s, 3 H), 3.68-3.65 (m, 2 H), 3.12 (br s, 2 H), 2.90-2.85 (m, 2 H), 2.82 (s, 3 H), 1.78-1.69 (m, 2 H).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.