Mohammad Ilyas
Aligarh Muslim University
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Publication
Featured researches published by Mohammad Ilyas.
Phytochemistry | 1998
Mehtab Parveen; Shafiullah Mohammad Sohrab Khan; Mohammad Ilyas
Abstract A novel flavone glycoside, luteolin 3′-O-β-xylosyl(1→2) glucoside, together with apigenin 7-xylosyl(1→2) glucoside has been isolated from V. grandifolium. The structure were elucidated by means of 1HNMR, 13CNMR, IR, UV and NOE spectral data.
Journal of Chemical Research-s | 2002
Mohammad Ilyas; Mehtab Perveen; Shafiullah; Syed Mohmud Ahmad
A novel chalcone 5′-bromo-2′-hydroxy-4,4′,6′-trimethoxy-chalcone, isoliquiritigenin-4,4′-dimethyl ether (2′-hydroxy-4,4′-dimethoxy chalcone) and 2′-hydroxy-3,4,4′,6′-tetramethoxy dihydrochalcone have been isolated from the leaves of Garcinia nervosa. Their structure have been elucidated on the basis of chemical and spectral evidences (1H NMR, 13C NMR, HMQC, NOE, IR, UV and mass spectra).
Tetrahedron | 1996
Mohammad Ilyas; Mehtab Parveen
Abstract 7,7′-dimethoxy-4,4′-dimethyl -3,3′-bicoumarin; 7,7′-dimethoxy-4,4′-dimethyl-3,6′-bicoumarin; 7,7′,8,8′-tetramethoxy-4,4′-dimethyl-3,3′-bicoumarin and 7,7′,8,8′-tetramethoxy-4,4′-dimethyl-3,5′-bicoumarin have been synthesized by the oxidation of 7-methoxy-4-methylcoumarin and 7,8-dimethoxy-4-methylcoumarin with Mn(OAc) 3 HClO 4 respectively.
Journal of The Chemical Society-perkin Transactions 1 | 1981
Mohammad Kamil; Mohammad Ilyas; W. Rahman; Noriko Hasaka; Masayoshi Okigawa; Nobusuke Kawano
Taiwaniaflavone (3,3′-linked biapigenin)(1) and its methyl ethers [(2) and (3)] isolated from the leaves of Taiwania cryptomerioides Hayata (Taxodiaceae) have been identified on the basis of spectral data and by synthesis of taiwaniaflavone methyl ethers [(5) and (29)]. Five known biflavones [(7), (8), (9), (10), and (11)] have also been isolated from the same plant.
Journal of Asian Natural Products Research | 2006
R. Kumar; Mohammad Ilyas; Mehtab Parveen; Shafiullah
A new chromone named as 5,4′-dihydroxy-7-methyl 3-benzyl chromone (1) along with three known flavonoid compounds as unsubstituted flavone, kaempferol-3-o-rhamnoside and quercetin-3-o-arabinoside have been isolated from the leaves of Cassia nodosa. Their structures have been established by means of chemical and spectral evidences (IR, UV, 1H-NMR, 13C-NMR and mass spectra).
Journal of Chemical Research-s | 1996
Shafiullah; Mohammad Sohrab Khan; Mehtab Parveen; Mohammad Kamil; Mohammad Ilyas
Journal of Chemical Research-s | 1994
Shafiullah; Mehtab Parveen; Mohammad Kamil; Mohammad Ilyas
Journal of Chemical Research-s | 1994
Mohammad Ilyas; Mehtab Parveen; Mohammed Sohrab Khan; Mohammad Kamil
Journal of Chemical Research-s | 1991
Neeru Jain; Mansoor Ahmad; Mohammad Kamil; Mohammad Ilyas
Journal of Chemical Research-s | 1991
Mansoor Ahmad; Neeru Jain; Mohammad Kamil; Mohammad Ilyas