A convenient method for the preparation of mono- and bis-substituted photochromic bis(benzothienyl)perfluorocyclopentenes via regioselective Friedel-Crafts acylation

Tetrahedron Letters

Volumn 53, Issue 44, 2012, Pages 5948-5951

  Bogacheva, A M ^a   Yarovenko, V N ^b   Levchenko, K S ^c   Kobeleva, O I ^d   Valova, T M ^d   Barachevsky, V A ^d   Struchkova, M I ^b   Shmelin, P S ^c   Krayushkin, M M ^b   Charushin, V N ^a  

^a INSTITUTE OF ORGANIC SYNTHESIS   (Russian Federation)

^b N D ZELINSKY INSTITUTE OF ORGANIC CHEMISTRY   (Russian Federation)

^c Central Science Research Institute of Technology 'Technomash'   (Russian Federation)

^d PHOTOCHEMISTRY CENTER   (Russian Federation)

Author keywords

Benzofurans; Bis(benzothienyl) hexafluorocyclopentenes; Photochromes; Regioselective Friedel Crafts acylation; Thiazoles

Indexed keywords

1,2 BIS(2 METHYLBENZO[B]THIEN 3 YL)HEXAFLUOROCYCLOPENTENE; BIS(BENZOTHIENYL)PERFLUOROCYCLOPENTENE DERIVATIVE; CYCLOPENTENE DERIVATIVE; KETONE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CYCLIZATION; FRIEDEL CRAFTS REACTION;

EID: 84866769372     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2012.08.111     Document Type: Article

References (17)

1. M. Irie Chem. Rev. 100 2000 1685 1716
2. K. Matsuda, and M. Irie Chem. Lett. 35 2006 1204 1209
3. M.M. Krayushkin, and M.A. Kalik Adv. Heterocycl. Chem. 103 2011 1 5
4. V.A. Barachevsky, and M.M. Krayushkin Russ. Chem. Bull. 57 2008 867 875
5. T. Yamaguchi, and M. Irie J. Photochem. Photobiol., A 178 2006 162 169
6. S. Pu, P. Yan, G. Liu, W. Miao, and W. Liu Tetrahedron Lett. 52 2011 143 147
7. T.J. Fukaminato Photochem. Photobiol., C 12 2011 177 208
8. C.M. Rayner, and N.A. Graham Science of Synthesis: Houben-Weyl Methods of Molecular Transformations 10 2000 Georg Thieme Stuttgart 155-184
9. S. Pal, M.A. Khan, P. Bindu, and P.K. Dubey Beilstein J. Org. Chem. 3 2007 35
10. V.N. Yarovenko, L.V. Khristoforova, L.I. Belen'kii, A.S. Shashkov, T.K. Baryshnikova, and M.M. rayushkin Chem. Heterocycl. Compd. 47 2011 166 172
11. V.N. Yarovenko, L.V. Khristoforova, L.I. Belenkii, N.D. Chuvylkin, and M.M. Krayushkin Russ. Chem. Bull. 11 2011 2270 2274
12. E. Kim, M. Kim, and K. Kim Tetrahedron 62 2006 6814 6821
13. S. Kobatake, M. Yamada, T. Yamada, and M. Irie J. Am. Chem. Soc. 121 1999 8450 8456
14. A.W. Erian, S.M. Sherif, and H.M. Gaber Molecules 8 2003 793 865
15. I.K. Moiseev, N.V. Makarova, and M.N. Zemtsova Russ. J. Org. Chem. 39 2003 1759 1773
16. U. Bora, A. Saikia, and R.C. Boruah Org. Lett. 5 2003 435 438
17. S.F. Gan, J.P. Wan, Y.J. Pan, and C.R. Sun Synlett 2010 973 975