Four Additional Meroterpenes Produced by Penicillium sp Found in Association with Melia azedarach. Possible Biosynthetic Intermediates to Austin

2007 ◽  
Vol 62 (8) ◽  
pp. 1035-1044 ◽  
Author(s):  
Taicia Pacheco Fill ◽  
Grace Kelli Pereira ◽  
Regina M. Geris dos Santos ◽  
Edson Rodrigues-Fo

Four additional meroterpenes were isolated and identified from rice cultures of Penicillium sp, a fungus obtained from the root bark of Melia azedarach. These new compounds were named preaustinoid B2 (1), preaustinoid A3 (2), austinolide (3), and isoaustinone (4) in analogy with the formerly described compounds. The structures were identified by extensive spectroscopic studies, including 1 D and 2 D NMR spectroscopy and HRMS. Compounds 1 - 4 are probably biosynthetic intermediates to Austin.

2003 ◽  
Vol 58 (9-10) ◽  
pp. 663-669 ◽  
Author(s):  
Regina M. Geris dos Santos ◽  
Edson Rodrigues-Fo.

AbstractFrom the methanolextract of Penicillium sp. cultivated on sterilized rice for three weeks we isolated three new meroterpenes preaustinoid A1, A2 and B1. The fungus was isolated from the root bark of Melia azedarach after surface sterilization. The structures of these compounds were identified by intensive spectroscopic studies.


2008 ◽  
Vol 59 (11) ◽  
Author(s):  
Miron Teodor Caproiu ◽  
Florea Dumitrascu ◽  
Mino R. Caira

New pyrrolo[1,2-b]pyridazine derivatives 8a-f were synthesized by 1,3-dipolar cycloaddition reaction between mesoionic 1,3-oxazolo[3,2-b]pyridazinium-2-oxides and diethyl or diisopropyl acetylenedicarboxylate as alkyne dipolarophiles. The structures of the new compounds were assigned by elemental analysis and NMR spectroscopy.


2008 ◽  
Vol 59 (10) ◽  
Author(s):  
Paul Ionut Dron ◽  
Neculai Doru Miron ◽  
Gheorghe Surpateanu

The paper presents the synthesis of cyclo (bis-paraquat p-phenylene p-phenylene-carbonyl) tetrakis (hexafluorophosphate), named �CETOBOX�, and the closely related structural determinations. This compound exists in three tautomeric forms. These forms were evidentiated by NMR-data (1H-NMR, TOCSY, COSY, NOESY), UV-Vis spectra coupled with pH measurements and by synthesis. As the �CETOBOX� gives �in situ� only the corresponding monoylide, the synthesis of a new fluorescent indolizine cyclophane has been performed by a 3+2 cycloaddition. All structures of the new compounds presented herein have been established by NMR spectroscopy. Also, theoretical methods (MM3, AM1, AM1-COSMO and B88LYPDFT) have been used to determine the most stable conformer structures.


2014 ◽  
Vol 10 ◽  
pp. 251-258 ◽  
Author(s):  
Louis P Sandjo ◽  
Eckhard Thines ◽  
Till Opatz ◽  
Anja Schüffler

Four new polyketides have been identified in culture filtrates of the fungal strain Penicillium sp. IBWF104-06 isolated from a soil sample. They are structurally based on the same trans-decalinpentanoic acid skeleton as tanzawaic acids A–H. One of the new compounds was found to inhibit the conidial germination in the rice blast fungus Magnaporthe oryzae at concentrations of 25 μg/mL.


2019 ◽  
Vol 10 (1) ◽  
pp. 26-29
Author(s):  
Ibtihal Hassan Hatim ◽  
Wasfi Aboud Al-Masoudi ◽  
Rashad Fadhil Ghadhban

There is an urgent need for the design and development of new and safer drugs, this has attracted organic chemists to synthesize new compounds with potential of biological and chemotherapeutic activities. Here we report, the condensation of phenylethylamine with 2-hydroxy naphthaldehyde yielded Schiff base derivative in good yield. Characterization of synthesized compound was carried by elemental analysis, IR, 1H-, 13C- and HSQC-NMR spectroscopy. The toxicity of the synthesized compound was determined using Balb/c mice model. Dixon’s up and down method was found to have an LD50 of 827.2 mg/kg of body weight, moderate toxicity.


1996 ◽  
Vol 51 (1) ◽  
pp. 133-138 ◽  
Author(s):  
Rolf Minkwitz ◽  
Ulrike Lohmann ◽  
Hans Preut

Abstract CH3S(0)C1 reacts in HF as solvent with MF5 (M = As, Sb) to give products CH3S(Cl)OMF5 (M = As, Sb). The new compounds are stable below 253 K and were charac­ terized by Raman and NMR spectroscopy.In addition, the crystal structure of CH3S(Cl)OSbCl5 has been determinated. The complex crystallizes in the monoclinic space group P21/n with a = 644.3(5), b = 1905.9(14), c = 900.0(7) pm, β = 99.27(6)° with four formula units per unit cell.


1981 ◽  
Vol 36 (12) ◽  
pp. 1532-1537 ◽  
Author(s):  
Jochen Ellermann ◽  
Martin Lietz

Abstract The reaction of l.l.l-tris(diiodarsinomethyl)ethane, CH3C(CH2Asl2)3 (1), with H2C(COOC2H5)2, H2C(COOCH3)2 and H2C(COC6H5)2 in presence of the auxiliary base (C2H5)3N gives the noradamantane structured compounds CH3C(CH2As)3E2 [E=C(COOC2H 5)2 (2), C(COOCH3)2 (3) and C(COC6H5)2 (4)].The new compounds have been characterized by mass spectrometry and infrared, Raman and 1H NMR spectroscopy.


1986 ◽  
Vol 41 (2) ◽  
pp. 185-190 ◽  
Author(s):  
Fritz Preuss ◽  
Flarald Becker

The compounds tC4H9N=VR(OtC4H9)2 (R = CH3, nC4H9, CH2SiMe3, Mes) and tC4H9N = VMes2(OtC4H9) have been prepared by reaction of tert-butyliminovanadium (V) chlorides with LiR; tC4H9N=V(CH2SiMe3)2(OtC4H9) and tC4H9N=VR3 (R = CH2SiMe3, Mes) could only be characterized by NMR spectroscopy. The 1H, 13C and 51V NMR spectra are discussed; the constants of 51V , 14N coupling have been determined.


2019 ◽  
Vol 34 (14) ◽  
pp. 2007-2013
Author(s):  
Qing-Mei Feng ◽  
Xing-Yu Li ◽  
Bing-Xin Li ◽  
Tian-Yuan Zhang ◽  
Hai-Feng Wang ◽  
...  

1982 ◽  
Vol 37 (5) ◽  
pp. 646-648 ◽  
Author(s):  
S. P. Perlepes ◽  
Th. F. Zafiropoulos ◽  
A. K. Anagnostopoulos ◽  
A. G. Galinos

The preparations of new compounds, containing the complex anions [Hg2l5]-, [Hg2l6]2- and [Hg3I8]2-, are reported.Distorted iodine-bridged configurations are proposed for the complexes in the solid state, utilising analyses, X-ray powder patterns, molar conductance measurements and spectral (IR, UV) data


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