Benzannulation

Tetrahedron

Volumn 64, Issue 48, 2008, Pages 10775-10790

  Kotha, Sambasivarao ^a   Misra, Shilpi ^a   Halder, Somnath ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY BOMBAY   (India)

Author keywords

Benzannulation; Cyclization; Cycloaddition; Diels Alder reaction; Rearrangement; Suzuki coupling, Metathesis

Indexed keywords

AROMATIC COMPOUND; BENZENE; CARBONYL DERIVATIVE; CHROMIUM; KETONE; LEWIS ACID; NAPHTHALENE; PALLADIUM; PHENANTHRENE; PHOSPHORUS; POLYCYCLIC AROMATIC HYDROCARBON; REBECCAMYCIN; RUTHENIUM;

ANNULATION REACTION; ANTINEOPLASTIC ACTIVITY; BENZANNULATION; BENZYLATION; CHEMICAL STRUCTURE; CYCLIZATION; CYCLOADDITION; DIELS ALDER REACTION; POLYMERIZATION; PRIORITY JOURNAL; REACTION ANALYSIS; REVIEW; RING CLOSING METATHESIS; VILSMEIER HAACK REACTION;

ALNUS;

EID: 53849135518     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.09.004     Document Type: Review

References (75)

1. Hervey R.G. Curr. Org. Chem. 8 (2004) 303-323
2. Hirsch A., and Brettreich M. Fullerenes Chemistry and Reactions (2005), Wiley-VCH, Weinheim
3. Monthioux M., and Kuznetsov V.L. Carbon 44 (2006) 1621-1623
4. Rodri{dotless}guez D., Castedo L., domi{dotless}nguez D., and Saa C. Org. Lett. 15 (2003) 3119-3121
5. Gupta A., Sen S., Harmata M., and Pulley S.R. J. Org. Chem. 70 (2005) 7422-7425
6. Asao N., Takahashi K., Lee S., Kasahara T., and Yamamoto Y. J. Am. Chem. Soc. 124 (2002) 12650-12651
7. Asao N., Nogami T., Lee S., and Yamamoto Y. J. Am. Chem. Soc. 125 (2003) 10921-10925
8. Asao N., and Aikawa H. J. Org. Chem. 71 (2006) 5249-5253
9. Barluenga J., Villa H.V., Ballesteros A., and González J.M. Org. Lett. 5 (2003) 4121-4123
10. Kotha S., and Ghosh A.K. Tetrahedron 60 (2004) 10833-10841
11. Kotha S., and Brahmachary E. Bioorg. Med. Chem. Lett. 7 (1997) 2719-2722
12. Kotha S., Ganesh T., and Ghosh A. Bioorg. Med. Chem. Lett. 10 (2000) 1755-1757
13. Kuroda S., Oda M., Zuo S., Kanayama K., Shah S.I.M., Furuta S., Miyatake R., and Kyogoku M. Tetrahedron Lett. 42 (2001) 6345-6348
14. Hayes M.E., Shinokubo H., and Danheiser R.L. Org. Lett. 7 (2005) 3917-3920
15. Paquette L., Lavrik P., and Karmer P. J. Org. Chem. 42 (1977) 503-507
16. Sygula A., Sygula R., and Rabideau P.W. Org. Lett. 8 (2006) 5909-5911
17. Grubbs R.H. Tetrahedron 60 (2004) 7117-7140
18. Kotha S., and Sreenivasachary N. Indian J. Chem. 40B (2001) 763-780
19. Schrock R.R., and Hoveyda A.H. Angew. Chem., Int. Ed. 42 (2003) 4592-4633
20. Fürstner A., Koch D., Langemann K., Leitner W., and Six C. Angew. Chem., Int. Ed. 36 (1997) 2466-2469
21. Pernerstorfer J., Schuster M., and Blechert S. Chem. Commun. (1997) 1949-1950
22. Kotha S., and Mandal K. Tetrahedron Lett. 45 (2004) 2585-2589
23. Kotha S., Shah V.R., and Mandal K. Adv. Synth. Catal. 349 (2007) 1159-1172
24. Iuliano A., Piccioli P., and Fabbri D. Org. Lett. 6 (2004) 3711-3714
25. Collins S.K., Grandbois A., Vachon M.P., and Cote J. Angew. Chem., Int. Ed. 45 (2006) 2923-2926
26. Bonifacio M.C., Robertson C.R., Jung J.-Y., and King B.T. J. Org. Chem. 70 (2005) 8522-8526
27. Pelly S.C., Parkinson C.J., Otterlo W.A.L., and de Koning C.B. J. Org. Chem. 70 (2005) 10474-10481
28. Katz T.J., and Sivavec T.M. J. Am. Chem. Soc. 107 (1985) 737-738
29. Kotha S., Sreenivasachary N., and Brahmachary E. Tetrahedron Lett. 39 (1998) 2805-2808
30. Kotha S., Halder S., and Brahmachary E. Tetrahedron 58 (2002) 9203-9208
31. Kotha S. Acc. Chem. Res. 36 (2003) 342-351
32. Kaliappan K., and Ravikumar V. Org. Biomol. Chem. 3 (2005) 848-851
33. Danheiser R.L., Takaki K., and Cha D. Org. Lett. 2 (2000) 3407-3410
34. Danheiser R.L., Zhang Y., and Austin W.F. Tetrahedron 64 (2008) 915-925
35. Danheiser R.L., Brisbois R.G., Kowalczyk J.J., and Millar R.F. J. Am. Chem. Soc. 112 (1990) 3093-3100
36. Danheiser R.L., Gee S.K., and Perez J.J. J. Am. Chem. Soc. 108 (1986) 806-810
37. Danheisr R.L., and Helgason A.L. J. Am. Chem. Soc. 116 (1994) 9471-9479
38. Danheiser R.L., Casebier D.S., and Firooznia F. J. Org. Chem. 60 (1995) 8341-8350
39. Smith A.B., Kozman S.A., and Adams C.M. J. Am. Chem. Soc. 122 (2000) 4984-4985
40. Kotha S., Brahmachary E., and Lahiri K. Eur. J. Org. Chem. (2005) 4741-4767
41. Kotha S., and Sreenivasachary N. Bioorg. Med. Chem. Lett. 10 (2000) 1413-1415
42. Kotha S., Mohanraja K., and Durani S. Chem. Commun. (2000) 1909-1910
43. Kotha S., and Sreenivasachary N. Eur. J. Org. Chem. (2001) 3375-3383
44. Shibata T., Yoshida S., Arai Y., and Endo K. Tetrahedron 64 (2008) 821-830
45. Agenet N., Buisine O., Slowinski F., Gandon V., and Malacria M. In: Overman L.E. (Ed). Organic Reactions Vol. 68 (2007), John Wiley & Sons, Hoboken 1
46. Chopade P.R., and Louie J. Adv. Synth. Catal. 348 (2006) 2107-2327
47. Yamamoto Y. Curr. Org. Chem. 9 (2005) 503-519
48. Tanaka K. Synlett (2007) 1977-1993
49. Panda K., Venkatesh C., Ila H., and Junjappa H. Eur. J. Org. Chem. (2005) 2045-2055
50. Hsung R.P., Buchanan G.S., Long Q.A., and Ghosh S.K. Tetrahedron 64 (2008) 883-893
51. Washakoon N., and Rigby J. J. Org. Chem. 61 (1996) 7644-7645
52. Brenna E., Fuganti C., Perozzo V., and Serra S. Tetrahedron 53 (1997) 15029-15040
53. Serra S., and Fuganti C. Synlett (1999) 1241-1242
54. Serra S. Synlett (2000) 890-892
55. Karus G.A., and Choudhury P.K. Synlett (2004) 97-98
56. Wurthwein E., Lyaskovskyy V., and Frohlich R. Synthesis 14 (2007) 2135-2144
57. Husein S., and Haddad N. Tetrahedron Lett. 38 (1997) 6087-6090
58. Hasegawa E., Y.Tamura, and Tosaka E. Chem. Commun. (1997) 1895-1896
59. Kim B.H., Lee J.G., Yim T., Kim H.-J., Lee H.Y., and Kim Y.G. Tetrahedron Lett. 47 (2006) 7727-7730
60. Burton D., Xu J., and Wang Y. J. Org. Chem. 71 (2006) 7780-7784
61. Minatti A., and Dötz K.H. J. Org. Chem. 70 (2005) 3745-3748
62. Danishefsky S., and Gordon D. J. Org. Chem. 57 (1992) 7052-7055
63. Watanabe M., Tanaka K., Saikawa Y., and Nakata M. Tetrahedron Lett. 48 (2007) 203-206
64. Shen H.-C., Tang J.-M., Chang H.-K., Yang C.-W., and Liu R.-S. J. Org. Chem. 70 (2005) 10113-10116
65. Shen H.-C., Pal S., Lian J.-J., and Liu R.-S. J. Am. Chem. Soc. 125 (2003) 15762-15763
66. Odedra A., Wu C.-J., Pratar T.B., Huang C.-W., Ran Y.-F., and Liu R.-S. J. Am. Chem. Soc. 127 (2005) 3406-3412
67. Nishii Y., Yoshida T., and Tanbe Y. Tetrahedron Lett. 38 (1997) 7195-7198
68. Nishii Y., and Tanbe Y. J. Chem. Soc., Perkin Trans. 1 (1997) 477-486
69. Rao S.C., and Rao G.S.K. Synthesis 3 (1987) 231-233
70. Raju B., and Rao G.S.K. Indian J. Chem. 26B (1987) 175-176
71. Ding W., Pu J., and Zhang C. Synthesis (1992) 635-637
72. Harrowven D.C., Bradley M., Castro J.L., and Flanagan S.R. Tetrahedron Lett. 42 (2001) 6973-6975
73. Terme T., Crozet M.P., Giraud L., and Vanelle P. Tetrahedron 56 (2000) 1097-1101
74. Tius M.A., and Galen J.G. Tetrahedron Lett. 27 (1986) 2571-2574
75. Langer P., Gorls H., Fischer C., and Hussain I. Tetrahedron 64 (2008) 864-900