Tandem Michael addition–Fries rearrangement of sorbylanilides: a convenient one pot synthesis of novel benzo[b]azocin-6-ones

[1]  Vipan Kumar,et al.  β‐Lactam‐Synthon‐Interceded, Facile, One‐Pot, Diastereoselective Synthesis of Functionalized Tetra/Octahydroisoquinolone Derivatives , 2011 .

[2]  Vipan Kumar,et al.  Diastereoselective approach to novel octahydroisoquinolones and an extension to its one-pot synthesis , 2010 .

[3]  Vipan Kumar,et al.  A regio and diastereoselective transformation of 3-dienyl-2-azetidinones to novel pyrroloxazine , 2010 .

[4]  B. Kaboudin,et al.  Fries Rearrangement of Anilides in the Presence of Phosphorus Pentoxide in Methanesulfonic Acid , 2009 .

[5]  M. P. Mahajan,et al.  REGIOSELECTIVE NITROSO DIELS-ALDER CYCLOADDITION REACTIONS OF 5-DIENYL PYRIMIDINONES AND TRANSFORMATION TO NOVEL 4-AMINO-ALCOHOL TETHERED PYRIMIDINONES , 2009 .

[6]  M. P. Mahajan,et al.  Regio- and π-facial selective Lewis acid interceded Diels–Alder reactions of α-dienyl-β-lactams: an indepth analysis , 2008 .

[7]  M. P. Mahajan,et al.  Lewis acid promoted imino Diels-Alder reactions of 5-dienyl pyrimidinones with N-aryl/naphthyl imines : synthesis of novel quinoline/benzoquinoline derivatives , 2008 .

[8]  M. P. Mahajan,et al.  A Facile Sodium Alkoxide Mediated Ring Opening of Unactivated a-Dienyl-b-lactams: Synthesis of Unnatural Multicomponent b-Aminodienoic Esters , 2007 .

[9]  B. Narasimhan,et al.  Quantitative structure-activity relationship studies for prediction of antimicrobial activity of synthesized 2,4-hexadienoic acid derivatives. , 2007, Bioorganic & medicinal chemistry letters.

[10]  Vipan Kumar,et al.  Lewis acid promoted aza Diels–Alder reactions of acyclic unactivated 5-dienyl pyrimidinones with N-arylimines: synthesis of novel quinoline derivatives , 2007 .

[11]  M. Taddei,et al.  Convenient synthetic approach to 2,4-disubstituted quinazolines. , 2007, Organic letters.

[12]  M. Taddei,et al.  Rapid approach to 3,5-disubstituted 1,4-benzodiazepines via the photo-fries rearrangement of anilides. , 2006, The Journal of organic chemistry.

[13]  Carol M. Taylor,et al.  The Anionic Phospho-Fries Rearrangement , 2004 .

[14]  J. Tepe,et al.  The First Intermolecular Friedel−Crafts Acylation with β-Lactams , 2002 .

[15]  B. Kaboudin.  Methanesulfonic acid/phosphorus oxychloride (MAPO) as a new efficient reagent in the Fries rearrangement , 1999 .

[16]  K. Pitchumani,et al.  FRIES REARRANGEMENT OF ESTERS IN MONTMORILLONITE CLAYS:STERIC CONTROL ON SELECTIVITY , 1997 .

[17]  D. Harrowven,et al.  Zirconium tetrachloride as a mediator for ambient temperature ortho-fries rearrangements , 1996 .

[18]  I. Hachiya,et al.  Hafnium trifluoromethanesulfonate (Hf(OTf)4) as an efficient catalyst in the fries rearrangement and direct acylation of phenol and naphthol derivatives , 1996 .

[19]  M. P. Mahajan,et al.  A Convenient Trans Diastereoselective Synthesis of 3-Butadienylazetidinones and Their Diels−Alder Cycloaddition Reactions , 1996 .

[20]  I. Hachiya,et al.  The catalytic Fries rearrangement of acyloxy naphthalenes using scandium trifluoromethanesulfonate as a catalyst , 1995 .

[21]  H. Sharghi,et al.  The mechanism of Fries rearrangement and acylation reaction in polyphosphoric acid , 1993 .

[22]  Robert J. Martin.  USES OF THE FRIES REARRANGEMENT FOR THE PREPARATION OF HYDROXYARYLKETONES. A REVIEW , 1992 .

[23]  Victor Snieckus,et al.  Directed ortho metalation. Tertiary amide and O-carbamate directors in synthetic strategies for polysubstituted aromatics , 1990 .

[24]  P. Demerseman,et al.  Titanium tetrachloride induced fries rearrangement: a new route to disubstituted 2'-hydroxypropiophenones , 1989 .

[25]  R. Sakai,et al.  New manzamine alkaloids from a sponge of the genus Xestospongia , 1988 .

[26]  Y. Ohizumi,et al.  Keramamine-A and -B, novel antimicrobial alkaloids from the Okinawan marine sponge sp. , 1987 .

[27]  R. Sakai,et al.  Manzamine A, a novel antitumor alkaloid from a sponge , 1986 .

[28]  C. Turba,et al.  Synthesis and pharmacological properties of N-derivatives of 5,6-dihydro-7H,12H-dibenz[c,f]azocine, a new tricyclic system. , 1968, Journal of medicinal chemistry.

[29]  A. Blatt.  The Fries Reaction , 1940 .