Conventional and Microwave-Assisted Syntheses and Solid-State Structure of New Coumarins and Angelicins

REFERENCES

• Hejchman , E. ; Maciejewska , D. ; Wolska , I. Microwave-assisted synthesis of derivatives of khellinone under phase-transfer catalytic conditions . Monatsh. Chem. 2008 , 139 , 1337 – 1348 .
   Google Scholar
• Trykowska , J. ; Hejchman , E. ; Wolska , I. ; Maciejewska , D. Solid state structure by x-ray and 13C CP/MAS NMR of new 7-[2-(N,N-diisopropylamino)ethoxy]coumarins . J. Mol. Struct. 2009 , 930 , 195 – 200 .
   Google Scholar
• Sardari , S. ; Mori , Y. ; Horita , K. ; Micetich , R. G. ; Nishibe , S. ; Danestalab , M. Synthesis and antifungal activity of coumarins and angular furanocoumarins . Bioorg. Med. Chem. 1999 , 7 , 1933 – 1940 .
   PubMed Web of Science ®Google Scholar
• Sardari , S. ; Nishibe , S. ; Danestalab , M. Coumarins, the bioactive structures with antifungal property . In Studies in Natural Products Chemistry ; Atta-ur-Rahman (Ed.); Elsevier : Amsterdam , 2000 ; vol. 23 , pp. 335 – 383 .
   Google Scholar
• Bordin , F. ; Baccichetti , F. ; Carlassare , F. ; Peron , M. ; Dall'Acqua , F. Pre-clinical evaluation of new antiproliferative agents for the photochemotherapy of psoriasis: Angelicin derivatives . Farmaco 1981 , 36 , 506 – 518 .
   Google Scholar
• Vedaldi , D. ; Dall'Acqua , F. ; Baccichetti , F. ; Carlassare , F. ; Bordin , F. Methylangelicins: Structure–activity studies on the role of methyl groups present in 3,4 and 4′,5′ photoreactive sites . Farmaco 1991 , 46 , 1381 – 1406 .
   PubMedGoogle Scholar
• Conconi , M. T. ; Montesi , F. ; Parnigotto , P. P. Antiproliferative activity and phototoxicity of some methyl derivatives of 5-methoxypsoralen and 5-methoxyangelicin . Pharm. Toxicol. 1998 , 82 , 193 – 198 .
   PubMedGoogle Scholar
• Bisagni , E. Synthesis of psoralenes and analogues . J. Photochem. Photobiol. B. 1992 , 14 , 23 – 46 .
   PubMedGoogle Scholar
• Zawadowski , T. ; Chęciński , M. Synthesis of new derivatives of angelicine of expected farmacological activity . Roczniki Chemii Ann. Soc. Chim. Polon. 1977 , 51 , 1511 – 1514 .
   Google Scholar
• Tolmachev , A. Y. ; Podkhalyuzina , N. Y. ; Kuznetsowa , N. A. ; Traven , V. F. New synthesis of 8-alkoxycarbonylangelicins . Rus. J. Org. Chem. 2001 , 37 , 1008 – 1012 ; Zhur. Org. Khim. 2001, 37, 1058–1062 .
   Google Scholar
• Valizadeh , H. ; Shockravi , A. Microwave-assisted Claisen rearrangement: Application to the synthesis of angelicin derivatives . J. Heterocycl. Chem. 2006 , 43 , 763 – 765 .
   Google Scholar
• Berendt , R. T. ; Sperger , D. M. ; Isbester , P. K. ; Munson , E. J. Solid-state NMR spectroscopy in pharmaceutical research and analysis . Trends Anal. Chem. 2006 , 25 , 977 – 984 .
   Web of Science ®Google Scholar
• Geppi , M. ; Mollica , G. ; Borsacchi , S. ; Veracini , C. A. Solid-state NMR studies of pharmaceutical systems . Apl. Spectr. Rev. 2008 , 43 , 202 – 302 .
   Web of Science ®Google Scholar
• HyperChem 7.02 . Hypercube Inc. : Waterloo , Ontario , Canada , 2002 .
   Google Scholar
• Frisch , M. J. ; Trucks , G. W. ; Schlegel , H. B. ; Scuseria , G. E. ; Robb , M. A. ; Cheeseman , J. R. ; Montgomery , Jr. , J. A. ; Vreven , A. ; Kudin , K. N. ; Burant , J. C. ; Millam , J. M. ; Iyengar , S. S. ; Tomasi , J. ; Barone , V. ; Menucci , B. ; Cossi , M. ; Scalmani , G. ; Rega , N. ; Petersson , G. A. ; Nakatsuji , H. ; Hada , M. ; Ehara , M. ; Toyota , K. ; Fukuda , R. ; Hasegawa , J. ; Ishida , M. ; Nakajima , T. ; Honda , Y. ; Kitao , O. ; Nakai , H. ; Klene , M. ; Li , X. ; Knox , J. E. ; Hratchian , H. P. ; Cross , J. B. ; Adamo , C. ; Jaramillo , J. ; Gomperts , R. ; Stratmann , R. E. ; Yazyev , O. ; Austin , A. J. ; Cammi , R. ; Pomelli , C. ; Ochterski , J. W. ; Ayala , P. Y. K. ; Morokuma , G. A. ; Voth , P. ; Salvador , J. J. ; Dannenberg , V. G. ; Zakrzewski , S. ; Dapprich , A. D. ; Daniels , M. C. ; Strain , O. ; Farkas , D. K. ; Malick , A. D. ; Rabuck , K. ; Raghavachari , J. B. ; Foresman , J. V. ; Ortiz , Q. ; Baboul , A. G. ; Clifford , S. ; Cioslowski , J. ; Stefanov , B. B. ; Liu , G. ; Liashenko , A. ; Piskorz , P. ; Komaromi , I. ; Martin , R. L. ; Fox , D. J. ; Keith , T. ; Al-Laham , M. A. ; Peng , C. Y. ; Nanayakkara , A. ; Challacombe , M. ; Gill , P. M. ; Johnson , W. B. ; Chen , W. ; Wong , M. W. ; Gonzalez , C. ; Pople , J. A. Gaussian 03, revision B.02. Gaussian, Inc. : Pittsburgh , PA , 2003.
   Google Scholar
• European Pharmacopoeia. 2008. Microbial assay of antibiotics, 6, 20702 (2.7.2) .
   Google Scholar
• National Committee for Clinical Laboratory Standards . Approved standard M7-A6: Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aerobically, , 6th ed. ; NCCLS : Wayne , PA , 2003 .
   Google Scholar