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DOI: 10.1055/s-0030-1258559
Synthesis of Organosulfur Compounds Based on Cyclocondensation Reactions of 3-Arylthio-1-silyloxy-1,3-butadienes and 1,3-Bis(silyloxy)-1,3-butadienes
Publication History
Publication Date:
03 September 2010 (online)
Abstract
Cyclocondensation reactions of sulfur-containing dienes, such as 3-arylthio-1-silyloxy-1,3-butadienes and 4-arylthio-1,3-bis(trimethylsilyloxy)-1,3-butadienes, with various dielectrophiles and dieneophiles allow for a convenient synthesis of a variety of functionalized and sterically encumbered aryl-substituted sulfides and sulfones which are not readily available by other methods. The building block strategy outlined herein is advantageous for the synthesis of highly substituted, sterically encumbered and functionalized molecules compared to methods which rely on the formation of a carbon-sulfur bond.
1 Introduction
2 3-Arylthio-1-trimethylsilyloxy-1,3-butadienes
2.1 Synthesis of 3-Arylthio-1-trimethylsilyloxy-1,3-butadienes
2.2 [3+3] Cyclocondensations of 3-Arylthio-1-trimethylsilyloxy-1,3-butadienes
2.2.1 1,1,3,3-Tetramethoxypropane
2.2.2 3-Silyloxy-2-en-1-ones
2.2.3 3-Alkoxy-2-en-1-ones
2.2.4 3-Ketoacetals
2.2.5 1,1-Diacylcyclopropanes
2.2.6 3-Oxo-orthoesters
2.2.7 1,1-Bis(methylthio)-1-en-3-ones
2.3 [4+2] Cycloadditions of 1-Arylthio-3-trimethylsilyloxy-1,3-butadienes
2.3.1 Dimethyl Acetylenedicarboxylate
2.3.2 Dimethyl Allene-1,3-dicarboxylate
2.4 Michael-Type Reactions of 1-Arythio-3-trimethylsilyloxy-1,3-butadienes
3 Cyclocondensations of 1,3-Bis(silyloxy)-1,3-butadienes with Sulfur-Containing Dielectrophiles
3.1 Reactions of 3-Alkoxy- and 3-Silyloxy-2-en-1-ones
3.1.1 2-Arylthio-3-silyloxy-2-en-1-ones
3.1.2 2-Arylthio-3-alkoxy-2-en-1-ones
3.1.3 2-Arylsulfonyl-3-alkoxy-2-en-1-ones
3.2 Reactions of 1,1-Bis(methylthio)-1-en-3-ones
4 4-Arylthio-1,3-bis(trimethylsilyloxy)-1,3-butadienes
4.1 Synthesis of 4-Arylthio-1,3-bis(trimethylsilyloxy)-1,3-butadienes
4.2 [3+3] Cyclizations of 4-Arylthio-1,3-bis(trimethylsilyloxy)-1,3-butadienes
4.2.1 1,1,3,3-Tetramethoxypropane
4.2.2 3-Silyloxy-2-en-1-ones
4.2.3 1,1-Diacetylcyclopropane
4.3 Cyclizations of 4-Arylthio-1,3-bis(silyloxy)-1,3-butadienes with Chromones
4.3.1 Formylchromone
4.3.2 Chromone
5 Conclusions
Key words
arenes - cyclizations - organosulfur compounds - silyl enol ethers
-
1a
Behar V.Danishefsky SJ. J. Am. Chem. Soc. 1993, 115: 7017 -
1b
Toste FD.Still IWJ. J. Am. Chem. Soc. 1995, 117: 7261 -
1c
Davidson BS.Molinski TF.Barrows LR.Ireland CM. J. Am. Chem. Soc. 1991, 113: 4709 -
1d
Mori Y.Taneda S.Hayashi H.Sakushima A.Kamata K.Suzuki AK.Yoshino S.Sakata M.Sagai M.Seki K.-i. Biol. Pharm. Bull. 2002, 25: 145 -
1e
Davis RA.Sandoval IT.Concepcion GP.Moreira da Rocha R.Ireland CM. Tetrahedron 2003, 59: 2855 -
1f
Liu H.Fujiwara T.Nishikawa T.Mishima Y.Nagai H.Shida T.Tachibana K.Kobayashi H.Mangindaan REP.Namikoshi M. Tetrahedron 2005, 61: 8611 -
1g
Kaplan ML.Reents WD. Tetrahedron Lett. 1982, 23: 373 -
1h
Hosoya Y.Adachi H.Nakamura H.Nishimura Y.Naganawa H. Tetrahedron Lett. 1996, 37: 9227 - Antibacterial activity:
-
2a
Shrimali SS.Joshi BC.Kishore D. J. Indian Chem. Soc. 1988, 65: 438 -
2b
Upadhyay PS.Vansdadia RN.Baxi AJ. Indian J. Chem. Sect. B 1990, 29: 793 - Inhibition of phospholipidase A2:
-
2c
Teshirogi I.Matsutani S.Shirahase K.Fujii Y.Yoshida T. J. Med. Chem. 1996, 39: 5183 - Inhibition of catechol O-methyltransferase:
-
2d
Paulini R.Lerner C.Diederich F.Jakob-Roetne R.Zuercher G.Borroni E. Helv. Chim. Acta 2006, 89: 1856 - Inhibition of dihydropteroate synthase of Escherichia coli:
-
2e
de Benedetti PG.Iarossi D.Menziani C.Caiolfa V.Frassineti C.Cennamo C. J. Med. Chem. 1987, 30: 459 -
2f
de Benedetti PG.Iarossi D.Folli U.Frassineti C.Menziani MC.Cennamo C. J. Med. Chem. 1989, 32: 2396 - Hypolipidemic activity:
-
2g
Sircar I.Hoefle M.Maxwell RE. J. Med. Chem. 1983, 26: 1020 - Cytotoxicity against HeLa cells and the antipicornavirus:
-
2h
Markley LD.Tong YC.Dulworth JK.Steward DL.Goralski CT. J. Med. Chem. 1986, 29: 427 - Neuropeptide Y1 receptor binding activity:
-
2i
Wright J.Bolton G.Creswell M.Downing D.Georgic L. Bioorg. Med. Chem. Lett. 1996, 6: 1809 - Anti-HIV activity:
-
2j
Neamati N.Mazumder A.Zhao H.Sunder S.Burke TR.Schultz RJ.Pommier Y. Antimicrob. Agents Chemother. 1997, 41: 385 -
2k
Chan JH.Hong JS.Hunter RN.Orr GF.Cowan JR.Sherman DB.Sparks SM.Reitter BE.Andrews CW.Hazen Richard J.Clair MS. J. Med. Chem. 2001, 44: 1866 -
2l
Tagat JR.McCombie SW.Steensma RW.Lin S.-I.Nazareno DV.Baroudy B.Vantuno N.Xu S.Liu J. Bioorg. Med. Chem. Lett. 2001, 11: 2143 - Anticholesteremic activity:
-
2m
Stanton JL.Cahill E.Dotson R.Tan J.Tomaselli HC.Wasvary JM.Stephan ZF.Steele RE. Bioorg. Med. Chem. Lett. 2000, 10: 1661 - Binding to human muscarinic M1 and M2 receptors:
-
2n
Kozlowski JA.Zhou G.Tagat JR.Lin S.-I.McCombie SW.Ruperto VB.Duffy RA.McQuade RA.Crosby G.Taylor LA.Billard W. Bioorg. Med. Chem. Lett. 2002, 12: 791 -
2o
Wang Y.Chackalamannil S.Hu Z.Clader JW.Greenlee W.Billard W.Binch H.Crosby G.Ruperto V.Duffy RA.McQuade R.Lachowicz JE. Bioorg. Med. Chem. Lett. 2000, 10: 2247 -
2p
Boyle CD.Chackalamannil S.Chen L.-Y.Dugar S.Pushpavanam P.Billard W.Binch H.Crosby G.Cohen-Williams M.Coffin VL.Duffy RA. Bioorg. Med. Chem. Lett. 2000, 10: 2727 -
2q
Wang Y.Chackalamannil S.Chang W.Greenlee W.Ruperto V.Duffy RA.McQuade R.Lachowicz JE. Bioorg. Med. Chem. Lett. 2001, 11: 891 -
2r
Boyle CD.Chackalamannil S.Clader JW.Greenlee WJ.Josien HB.Kaminski JJ.Kozlowski JA.McCombie SW.Nazareno DV.Tagat JR.Wang Y. Bioorg. Med. Chem. Lett. 2001, 11: 2311 -
2s
Boyle CD.Vice SF.Campion J.Chackalamannil S.Lankin CM.McCombie SW.Billard W.Binch H.Crosby G.Williams M.-C.Coffin VL. Bioorg. Med. Chem. Lett. 2002, 12: 3479 - Histamine H3 receptor antagonistic activity:
-
2t
Sasse A.Ligneau X.Sadek B.Elz S.Pertz HH.Ganellin CR.Arrang J.-M.Schwartz J.-C.Schunack W.Stark H. Arch. Pharm. (Weinheim Ger.) 2001, 334: 45 - Antiprotozoal activity:
-
2u
Langler RF.Paddock RL.Thompson DB.Crandall I.Ciach M.Kain KC. Aust. J. Chem. 2003, 56: 1127 - Binding to neuroblastoma cells:
-
2v
Clark RD.Jahangir A.Severance D.Salazar R.Chang T.Chang D.Jett MF.Smith S.Bley K. Bioorg. Med. Chem. Lett. 2004, 14: 1053 - Binding to the human cannabinoid CB1 receptor:
-
2w
Lavey BJ.Kozlowski JA.Hipkin RW.Gonsiorek W.Lundell DJ.Piwinski JJ.Narula S.Lunn CA. Bioorg. Med. Chem. Lett. 2005, 15: 783 - Inhibition of the main protease of the recombinant SARS coronavirus:
-
2x
Lu I.-L.Mahindroo N.Liang P.-H.Peng Y.-H.Kuo C.-J.Tsai K.-C.Hsieh H.-P.Chao Y.-S.Wu S.-Y. J. Med. Chem. 2006, 9: 5154 -
3a
Glass HB.Reid EE. J. Am. Chem. Soc. 1929, 51: 3428 -
3b
Dougherty G.Hammond PD. J. Am. Chem. Soc. 1935, 57: 117 - For the trifluoromethanesulfonic acid catalyzed sulfurization of cycloalkanes, see:
-
3c
Olah GA.Wang Q.Prakash GKS. J. Am. Chem. Soc. 1990, 112: 3697 -
3d
Kemp DS.Carey RI.Dewan JC.Galakatos NG.Kerkman D.Leung S.-L. J. Org. Chem. 1989, 54: 1589 ; and references cited therein -
3e
Chua M.Hoyer H. Z. Naturforsch. B 1965, 20: 416 -
3f
Baxter I.Ben-Haida A.Colquhoun HM.Hodge P.Kohnke FH.Williams DJ. Chem. Eur. J. 2000, 6: 4285 ; and references cited therein -
3g
Campbell JR. J. Org. Chem. 1964, 29: 1830 -
4a
Taniguchi N. J. Org. Chem. 2007, 72: 1241 -
4b
Fernández-Rodríguez MA.Shen Q.Hartwig JF. J. Am. Chem. Soc. 2006, 128: 2180 -
4c
Murata M.Buchwald SL. Tetrahedron 2004, 60: 7397 -
4d
Gendre F.Yang M.Diaz P. Org. Lett. 2005, 7: 2719 -
4e
Bates CG.Gujadhur RK.Venkataraman D. Org. Lett. 2002, 4: 2803 -
4f
Rábai J. Synthesis 1989, 523 -
5a
Joseph JK.Jain SL.Sain B. Synth. Commun. 2006, 36: 2743 -
5b
Chen D.-W.Kubiak RJ.Ashley JA.Janda KD. J. Chem. Soc., Perkin Trans. 1 2001, 21: 2796 -
5c
Marquie J.Laporterie A.Dubac J.Roques N.Desmurs J.-R. J. Org. Chem. 2001, 66: 421 -
5d
Repichet S.Roux CL.Dubac J. Tetrahedron Lett. 1999, 40: 9233 -
5e
Hajipour AR.Zarei A.Khazdooz L.Pourmousavi SA.Mirjalili BBF.Ruoho AE. Phosphorus Sulfur Silicon Relat. Elem. 2005, 180: 2029 -
5f
Woroshzow V.Kutschkarow V. Zh. Obshch. Khim. 1949, 19: 1943 ; Chem. Abstr. 1950, 1922 -
6a
Zhu W.Ma D. J. Org. Chem. 2005, 70: 2696 -
6b
Bandgar BP.Bettigeri SV.Phopase J. Org. Lett. 2004, 6: 2105 -
6c
Huang F.Batey RA. Tetrahedron 2007, 63: 7667 -
7a
Hilt G.Lüers S. Synthesis 2003, 1784 -
7b
Hilt G.Lüers S.Harms K. J. Org. Chem. 2004, 69: 624 -
8a
Erian AW.Issac Y.Sherif SM.Mahmoud FF. J. Chem. Soc., Perkin Trans. 1 2000, 3686 -
8b
Ogura K.Takeda M.Xie JR.Akazome M.Matsumoto S. Tetrahedron Lett. 2001, 42: 1923 -
8c
Matsumoto S.Kumazawa K.Ogura K. Bull. Chem. Soc. Jpn. 2003, 76: 2179 -
8d
Bianchi L.Dell’Erba C.Maccagno M.Mugnoli A.Novi M.Petrillo G.Sancassan F.Tavani C. J. Org. Chem. 2003, 68: 5254 -
8e
Mutsuhiro Y.Watanabe M.Furukawa S. Chem. Pharm. Bull. 1990, 38: 902 -
8f
Padwa A.Gareau Y.Harrison B.Rodriguez A. J. Org. Chem. 1992, 57: 3540 -
8g
Hayakawa K.Nishiyama H.Kanematsu K. J. Org. Chem. 1985, 50: 512 -
8h
Nakayama J.Hirashima A. J. Am. Chem. Soc. 1990, 112: 7648 -
8i
Hu C.-M.Hong F.Jiang B.Xu Y. J. Fluorine Chem. 1994, 66: 215 -
8j
Antelo B.Castedo L.Delamano J.Gomes A.Lopez C.Tojo G. J. Org. Chem. 1996, 61: 1188 -
8k
Bull JR.Desmond-Smith NS.Heggie SJ.Hunter R.Tien F.-C. Synlett 1998, 900 - 9
Chan TH.Prasad CVC. J. Org. Chem. 1986, 51: 3012 - 10
Imran M.Iqbal I.Rasool N.Rashid MA.Langer P. Synlett 2008, 2708 - 11
Imran M.Iqbal I.Rasool N.Fischer C.Langer P. Tetrahedron 2009, 65: 8794 - 12
Iqbal I.Imran M.Langer P. Helv. Chim. Acta 2010, in print - 13
Iqbal I.Imran M.Shkoor M.Fatunsin O.Riahi A.Villinger A.Fischer C.Langer P. Tetrahedron 2010, submitted - 14
Iqbal I.Imran M.Villinger A.Langer P. Synthesis 2009, 297 - 15
Andersson C.-M.Hallberg A. J. Org. Chem. 1988, 53: 4257 - 16
Rashid MA.Rasool N.Iqbal I.Imran M.Langer P. Tetrahedron Lett. 2008, 49: 2466 - 17
Danishefsky SJ. Acc. Chem. Res. 1979, 66 - 18
Zefirov NS.Kozhushkov SI.Kuznetsova TS. Tetrahedron 1982, 38: 1693 - 19
Imran M.Iqbal I.Langer P. Synlett 2009, 1477 - 20
Iqbal I.Imran M.Langer P. Synthesis 2009, 2430 - 21
Iqbal I.Imran M.Fischer C.Langer P. Helv. Chim. Acta 2010, 93: 704 -
22a
Prasad CVC.Chan TH. J. Org. Chem. 1987, 52: 110 -
22b
Prasad CVC.Chan TH. J. Org. Chem. 1987, 52: 120 -
22c
Prasad CVC.Chan TH. J. Org. Chem. 1989, 54: 3242 -
22d
Schwerdtfeger AE.Chan TH.
J. Org. Chem. 1993, 58: 6513 -
23a
Chan T.-H.Brownbridge P. J. Am. Chem. Soc. 1980, 102: 3534 -
23b
Brownbridge P.Chan T.-H.Brook MA.Kang GJ. Can. J. Chem. 1983, 61: 688 - 24 For a review on [3+3] cyclocondensations
of 1,3-bis(silyl enol ethers) with 1,3-dielectrophiles, see:
Feist H.Langer P. Synthesis 2007, 327 - 25
Rashid MA.Reinke H.Langer P. Tetrahedron Lett. 2007, 48: 2321 - 26
Rashid MA.Rasool N.Adeel M.Reinke H.Fischer C.Langer P. Tetrahedron 2008, 64: 3782 - 27
Shkoor M.Fatunsin O.Riahi A.Villinger A.Langer P. Tetrahedron Lett. 2009, 50: 5726 - 28
Fatunsin O.Shkoor M.Riahi A.Hussain M.Villinger A.Fischer C.Langer P. Helv. Chim. Acta 2010, in print - 29
Riahi A.Shkoor M.Fatunsin O.Lubbe M.Reinke H.Langer P. Tetrahedron Lett. 2009, 50: 115 - 30
Shkoor M.Riahi A.Fatunsin O.Reinke H.Fischer C.Langer P. Synthesis 2009, 2223 - 31
Lubbe M.Klassen R.Trabhardt T.Villinger A.Langer P. Synlett 2008, 2331 - 32
Sher M.Ahmed Z.Rashid MA.Fischer C.Langer P. J. Org. Chem. 2007, 72: 6284 - 33
Appel B.Rotzoll S.Reinke H.Langer P. Eur. J. Org. Chem. 2006, 3638 - 34
Appel B.Saleh NNR.Langer P. Chem. Eur. J. 2006, 12: 1221