En route towards α-benzotriazoyl nitroso derivatives

Monbaliu, Jean-Christophe; Beagle, Lucas; Kovacs, Judit; Zeller, Matthias; Stevens, Christian; Katritzky, Alan

doi:10.1039/c2ra21311g

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Article (Scientific journals)

En route towards α-benzotriazoyl nitroso derivatives

Monbaliu, Jean-Christophe; Beagle, Lucas; Kovacs, Judit et al.

2012 • In RSC Advances, 2, p. 8941-8945

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10.1039/c2ra21311g

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Keywords :

α-benzotriazoyl nitroso derivativves; NO donor; DFT

Disciplines :

Chemistry

Author, co-author :

Monbaliu, Jean-Christophe ; University of Florida - UF > Department of Chemistry > Center for Heterocyclic Compounds

Beagle, Lucas; University of Florida - UF > Department of Chemistry > Center for Heterocyclic Compounds

Kovacs, Judit; University of Florida - UF > Department of Chemistry > Center for Heterocyclic Compounds

Zeller, Matthias; Youngstown State University > Department of Chemistry

Stevens, Christian; Universiteit Gent - Ugent > Department of Sustainable Organic Chemistry and Technology > SynBioC Research Group

Katritzky, Alan; University of Florida - UF > Department of Chemistry > Center for Heterocyclic Compounds

Language :

English

Title :

En route towards α-benzotriazoyl nitroso derivatives

Publication date :

2012

Journal title :

RSC Advances

eISSN :

2046-2069

Publisher :

Royal Society of Chemistr, United Kingdom

Volume :

Pages :

8941-8945

Peer reviewed :

Peer Reviewed verified by ORBi

Available on ORBi :

since 06 January 2014

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B. S. Bodnar M. J. Miller Angew. Chem., Int. Ed. 2011 50 5630 5647
H. Yamamoto M. Kawasaki Bull. Chem. Soc. Jpn. 2007 80 595 607
Y. Yamamoto H. Yamamoto Eur. J. Org. Chem. 2006 2031 2043
S. Iwasa A. Fakhruddin H. Nishiyama Mini-Rev. Org. Chem. 2005 2 157 175
H. Yamamoto N. Momiyama Chem. Commun. 2005 3514 3525
D. Chaiyaveij L. Cleary A. S. Batsanov T. B. Marder K. J. Shea A. Whiting Org. Lett. 2011 13 3442 3445
J. M. de los Santos R. Ignacio G. Rubiales D. Aparicio F. Palacios J. Org. Chem. 2011 76 6715 6725
T. A. Wencewicz B. Yang J. R. Rudloff A. G. Oliver M. J. Miller J. Med. Chem. 2011 54 6843 6858
A. Yanagisawa T. Fujinami Y. Oyokawa T. Sugita K. Yoshida Org. Lett. 2012 14 2434 2437
V. Krchnak J. Zajícek P. A. Miller M. J. Miller J. Org. Chem. 2011 76 10249 10253
C. P. Frazier J. R. Engelking J. Read de Alaniz J. Am. Chem. Soc. 2011 133 10430 10433
K. Shen X. Liu G. Wang L. Lin X. Feng Angew. Chem., Int. Ed. 2011 50 4684 4688
M. Nielsen D. Worgull T. Zweifel B. Gschwend S. Bertelsen K. A. Jørgensen Chem. Commun. 2011 47 632 649
S. Murru A. A. Gallo R. S. Srivastava ACS Catal. 2011 1 29 31
P. Sancibrao D. Karila C. Kouklovsky G. Vincent J. Org. Chem. 2010 75 4333 4336
P.-H. Lu C.-S. Yang B. Devendar C.-C. Liao Org. Lett. 2010 12 2642 2645
G. R. Stephenson A. M. Balfe D. L. Hughes R. D. Kelsey Tetrahedron Lett. 2010 51 6806 6809
W. Lin K. G. Virga K.-H. Kim J. Zajicek D. Mendel M. J. Miller J. Org. Chem. 2009 74 5941 5946
C. Kibayashi Chem. Pharm. Bull. 2005 53 1375 1386
A. Hall P. D. Bailey D. C. Rees G. M. Rosair R. H. Wightman J. Chem. Soc., Perkin Trans. 1 2000 329 343
T. Faitg J. Soulié J.-Y. Lallemand L. Ricard Tetrahedron: Asymmetry 1999 10 2165 2174
A. Hall P. D. Bailey D. C. Rees R. H. Wightman Chem. Commun. 1998 2251 2252
W. Oppolzer O. Tamura G. Sundarababu M. Signer J. Am. Chem. Soc. 1992 114 5900 5902
W. Oppolzer O. Tamura Tetrahedron Lett. 1990 31 991 994
H. Iida Y. Watanabe C. Kibayashi Tetrahedron Lett. 1984 25 5091 5094
N. J. Leonard A. J. Playtis F. Skoog R. Y. Schmitz J. Am. Chem. Soc. 1971 93 3056 3058
B. Belleau Y.-K. Au-Young J. Am. Chem. Soc. 1963 85 64 71
J.-C. Monbaliu G. Dive J. Marchand-Brynaert D. Peeters THEOCHEM 2010 959 49 54
J. Streith A. Defoin Synthesis 1994 11 1107 1117
M. E. Shoman J. F. DuMond T. S. Isbell J. H. Crawford A. Brandon J. Honovar D. A. Vitturi C. R. White R. P. Patel S. B. King J. Med. Chem. 2011 54 1059 1070
J. F. DuMond S. B. King Antioxid. Redox Signaling 2011 14 1637 1648
H. Chakrapani M. D. Bartberger E. J. Toone J. Org. Chem. 2009 74 1450 1453
X. Sha T. S. Isbell R. P. Patel C. S. Day S. B. King J. Am. Chem. Soc. 2006 128 9687 9692
A. Di Stilo C. Medana B. Ferrarotti A. L. Gasco D. Ghigo A. Bosia P. A. Martorana A. Gasco Pharmacol. Res. 2000 41 469 474
R. Bou-Moreno S. Luengo-Arratta W. B. Motherwell Tetrahedron Lett. 2011 52 2097 2099
G. Calvet S. C. Coote N. Blanchard C. Kouklovsky Tetrahedron 2010 66 2969 2980
H. Li D. Gori C. Kouklovsky G. Vincent Tetrahedron: Asymmetry 2010 21 1507 1510
G. Calvet M. Dussaussois N. Blanchard C. Kouklovsky Org. Lett. 2004 6 2449 2451
V. Gouverneur L. Ghosez Tetrahedron 1996 52 7585 7598
J.-C. M. Monbaliu F. K. Hansen L. K. Beagle M. J. Panzner P. J. Steel E. Todadze C. V. Stevens A. R. Katritzky Chem.-Eur. J. 2012 18 2632 2638
A. R. Katritzky P. Angrish E. Todadze Synlett 2009 2392 2411
A. R. Katritzky B. V. Rogovoy Chem.-Eur. J. 2003 9 4586 4593
A. R. Katritzky X. Lan J. Z. Yang O. V. Denisko Chem. Rev. 1998 98 409 548
N. Stellenboom R. Hunter M. R. Caira Tetrahedron 2010 66 3228 3241
R. Hunter M. Caira N. Stellenboom J. Org. Chem. 2006 71 8268 8271
K. Ganapathy R. Gurumurthy N. Mohan G. Sivagnanam Monatsh. Chem. 1987 118 583 587
C. W. Rees R. C. Storr J. Chem. Soc. (C) 1969 1474 1477
T. V. Hughes S. D. Hammond M. P. Cava J. Org. Chem. 1998 63 401 402
L. R. Domingo P. Pérez Org. Biomol. Chem. 2011 9 7168 7175
L. R. Domingo J. A. Sáez Org. Biomol. Chem. 2009 7 3576 3583
L. R. Domingo E. Chamorro P. Pérez J. Org. Chem. 2008 73 4615 4624
L. R. Domingo J. A. Sáez P. Pérez Chem. Phys. Lett. 2007 438 341 345
M. J. Aurell L. R. Domingo P. Pérez R. Contreras Tetrahedron 2004 60 11503 11509
P. Perez L. R. Domingo M. J. Aurell R. Contreras Tetrahedron 2003 59 3117 3125
L. R. Domingo P. Perez R. Contreras J. Org. Chem. 2003 68 6060 6062
L. R. Domingo M. J. Aurell P. Pérez R. Contreras Tetrahedron 2002 58 4417 4423
R. R. Contreras P. Fuentealba M. Galvan P. Perez Chem. Phys. Lett. 1999 304 405 413
A. H. A. Mohammed G. Nagendrappa J. Chem. Sci. 2010 122 571 577
A. O. Terent'ev I. B. Krylov Y. N. Ogibin G. I. Nikishin Synthesis 2006 22 3819 3824
A. K. Gupta J. Acharya D. Pardasani D. K. Dubey Tetrahedron Lett. 2007 48 767 770
V. Kumar M. P. Kaushik Tetrahedron Lett. 2005 46 8121 8123
A. Zaks A. V. Yabannavar D. R. Dodds C. Anderson Evans P. R. Das R. Malchow J. Org. Chem. 1996 61 8692 8695
H. Diekmann W. Luttke Angew. Chem., Int. Ed. Engl. 1968 7 387 388
M. A. McCarrick Y.-dong Wu K. N. Houk J. Am. Chem. Soc. 1992 114 1499 1500
I. V. Alabugin K. M. Gilmore P. W. Peterson Wiley Interdiscip. Rev.: Comput. Mol. Sci. 2011 1 109 141
A. E. Reed L. A. Curtiss F. Weinhold Chem. Rev. 1988 88 899 926
G. Kaupp J. Schmeyers J. Org. Chem. 1995 60 5494 5503
M. L. Coote C. Y. Lin A. L. J. Beckwith A. A. Zavitsas Phys. Chem. Chem. Phys. 2010 12 9597 9610
N. Shao X.-G. Sun S. Dai D.-en Jiang J. Phys. Chem. B 2012 116 3235 3238
N. Shao X.-G. Sun S. Dai D.-en Jiang J. Phys. Chem. A 2011 115 12120 12125
Y. Ogata T. Akada Tetrahedron 1972 28 15 19
T. G. Bonner R. A. Hancock J. Chem. Soc. (B) 1970 519 524
K. M. Ibne-Rasa C. G. Lauro E. J. O J. Am. Chem. Soc. 1963 85 1165 1167
P. Astolfi P. Carloni E. Damiani L. Greci M. Marini C. Rizzoli P. Stipa Eur. J. Org. Chem. 2008 3279 3285
B. G. Gowenlock B. King J. Pfab M. Witanowski J. Chem. Soc., Perkin Trans. 2 1998 483 485
B. G. Gowenlock J. Pfab V. M. Young J. Chem. Soc., Perkin Trans. 2 1997 1793 1798
G. L. Squadrito F. R. Fronczek S. F. Watkins D. F. Church W. A. Pryor J. Org. Chem. 1990 55 4322 4326