Synthetic approaches to activated pyrrolo[3,2,1-hi]indoles: synthesis of 6,8-dimethoxy pyrrolo[3,2,1-hi]indole

Tetrahedron

Volumn 65, Issue 12, 2009, Pages 2591-2598

  Jumina, ^a   Kumar, Naresh ^a   Black, David St C ^a  

^a UNIVERSITY OF NEW SOUTH WALES   (Australia)

Author keywords

Dehydrogenation; Indoles; Isatins; Pyrroloindoles

Indexed keywords

6,8 DIMETHOXY PYRROLO[3,2,1 HI]INDOLE; INDOLE DERIVATIVE; ISATIN; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CRYSTAL STRUCTURE; CYCLIZATION; DEHYDROGENATION; PRIORITY JOURNAL; REDUCTION KINETICS; RING OPENING; SUBSTITUTION REACTION;

EID: 60149111738     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.01.010     Document Type: Article

References (23)

1. Jumina; Keller P.A., Kumar N., and Black D.St.C. Tetrahedron 64 (2008) 11603-11610
2. Black D.St.C., Keller P.A., and Kumar N. Tetrahedron 48 (1992) 7601-7608
3. Martinez A.G., Alvarez R.M., Barcina J.O., Cerero S.M., Vilar E.T., Fraile A.G., Hanack M., and Subramanian L.R. J. Chem. Soc., Chem. Commun. (1990) 1571-1572
4. Meth-Cohn O., and Staniforth S.P. In: Heathcock C.H. (Ed). Comprehensive Organic Chemistry Vol. 2 (1991), Pergamon, Oxford 777-794
5. Sugasawa T., Adachi M., Sasakura K., and Kitagawa A. J. Org. Chem. 44 (1979) 578-586
6. Anthony W.C. J. Org. Chem. 25 (1960) 2049-2053
7. Brown V.H., Skinner W.A., and De Graw J.I. J. Heterocycl. Chem. 6 (1969) 539-543
8. Newman H., and Angier R.B. J. Org. Chem. 34 (1969) 3484-3491
9. Gribble G.W., and Hoffman J.H. Synthesis (1977) 859-860
10. Gribble G.W., and Nutaitis C.F. Org. Prep. Proced. Int. 17 (1985) 317-384
11. Gribble G.W., Lord P.D., Skotnicki J., Dietz S.E., Eaton J.T., and Johnson J.L. J. Am. Chem. Soc. 96 (1974) 7812-7814
12. Kumar Y., and Florvall L. Synth. Commun. 13 (1983) 489-493
13. Valls N., Bonjoch J., and Bosch J. J. Org. Chem. 57 (1992) 2508-2511
14. Marshall J.A., and Johnson W.S. J. Org. Chem. 28 (1963) 595-596
15. Hach V. Synthesis (1974) 341-342
16. Paudler W.W., and Shin H.G. J. Heterocycl. Chem. 6 (1969) 415-417
17. Black D.St.C., Bowyer M.C., Bowyer P.K., Ivory A.J., Kim M., Kumar N., McConnell D.B., and Popiolek M. Aust. J. Chem. 47 (1994) 1741-1750
18. Black D.St.C., Kumar N., and Wong L.C.H. Aust. J. Chem. 39 (1986) 15-20
19. Black D.St.C., Gatehouse B.M.K.C., Theobald F., and Wong L.C.H. Aust. J. Chem. 33 (1980) 343-350
20. In: Ibers J.A., and Hamilton W.C. (Eds). International Tables for X-Ray Crystallography Vol. 4 (1974), Kynoch, Birmingham
21. Altomare A., Burla M.C., Camalli M., Cascarano G., Giacovazzo C., Guagliardi A., and Polidori G. J. Appl. Crystallogr. 27 (1994) 435-440
22. Rae A.D. RAELS. A comprehensive Least Squares Refinement Program (1996), University of New South Wales, Sydney
23. Johnson C.K. ORTEP-II (1976), Oak Ridge National Laboratory, Oak Ridge, TN