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Volumn 47, Issue 15, 2006, Pages 2605-2606

Two-step synthesis of the bipyrrole precursor of prodigiosins

Author keywords

Bipyrrole; Haloformylation; Natural product; Prodigiosins; Suzuki coupling; Tambjamines

Indexed keywords

4 METHOXY 2,2' BIPYRROLE 5 CARBOXALDEHYDE; 4 METHOXY 3 PYRROLIN 2 ONE; PRODIGIOSIN; PYRROLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33644898091     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.02.035     Document Type: Article
Times cited : (61)

References (16)
  • 9
    • 84942714694 scopus 로고
    • It has been previously shown that increasing the size of R groups in the formylating reagent can be beneficial for controlling regioselectivity and change the ratio of the possible products: For example: S. Pansare, and G. Ravi Synlett 10 1994 823 824
    • (1994) Synlett , vol.10 , pp. 823-824
    • Pansare, S.1    Ravi, G.2
  • 10
    • 33644910046 scopus 로고    scopus 로고
    • note
    • 3): δ (ppm) 1.24-1.37 (6H, m), 3.31-3.46 (2H, q, J = 7.1), 3.76 (3H, s), 4.03-4.18 (2H, q, J = 7.1), 5.58 (1H, s), 6.98 (1H, s). HRMS; m/z: 259.0440 [M+1]. Found: 259.0443.
  • 13
    • 33644900115 scopus 로고    scopus 로고
    • note
    • 6): δ (ppm) 3.82 (3H, s), 6.10 (1H, t, J = 2.9), 6.26 (1H, s), 6.73 (1H, d, J = 2.6), 6.89 (1H, br s), 9.27 (1H, s), 11.13-11.29 (1H, br s), 11.32-11.49 (1H, br s). HRMS; m/z: 191.0815 [M+1]. Found: 191.0807.
  • 14
    • 33644929176 scopus 로고    scopus 로고
    • Produced by MDS Pharma Services, South Bothell WA, USA.
    • Produced by MDS Pharma Services, South Bothell WA, USA.
  • 16
    • 33644896414 scopus 로고    scopus 로고
    • note
    • 2-[2-[(3,5-Dimethyl-1H-pyrrol-2-yl)methylene]-3-methoxy-2H-pyrrol-5-yl] -1H-indole.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.