Reactions of indole-2,3-dione 1 with 2-mercaptobenzimidazole, o-phenylenediamine, 2- aminophenol, 2-aminobenzothiazole, 2-aminobenzimidazole and 3-methyl-1-phenyl-2- pyrazolin-5-one were carried out to give compounds spiroindolethiazetobenzimidazole 2, spirobenzimidazole(oxazole)indoline 3a,b, benzothiazol(imidazol) iminoindolinone 4a,b and methyloxoindolylidenepyrazolone 5 respectively. Compound 5 was reacted with 2- aminophenol as well as o-phenylenediamine to give new spirooxazepine and diazepine derivatives 6a,b respectively. Reaction of 5 with nitrogen nucleophiles as well as carbon nucleophiles was investigated to furnish new spiro heterocycles 7-11. The reaction of 2-(2- oxo-1,2-dihydroindol-3-ylidene)malononitrile compound 12 with 3-methyl-1-phenyl-2- pyrazoline-5-one was carried out to give spiroindolopyranopyrazolo derivative 13. Compounds 4a,b was reacted with thioglycolic acid to give thiazolidinone derivatives 14a,b. Epoxidation of 5 using monoperoxyphthalic acid magnesium salt hexahydrate and hydrogen peroxide were executed to afford the novel dispiro (2-pyrazolin oxiraneindoline)dione compound 15. The chemical structures of the synthesized compounds were well established by elemental and spectral analyses.

Reactions of indole-2,3-dione 1 with 2-mercaptobenzimidazole, o-phenylenediamine, 2- aminophenol, 2-aminobenzothiazole, 2-aminobenzimidazole and 3-methyl-1-phenyl-2- pyrazolin-5-one were carried out to give compounds spiroindolethiazetobenzimidazole 2, spirobenzimidazole(oxazole)indoline 3a,b, benzothiazol(imidazol) iminoindolinone 4a,b and methyloxoindolylidenepyrazolone 5 respectively. Compound 5 was reacted with 2- aminophenol as well as o-phenylenediamine to give new spirooxazepine and diazepine derivatives 6a,b respectively. Reaction of 5 with nitrogen nucleophiles as well as carbon nucleophiles was investigated to furnish new spiro heterocycles 7-11. The reaction of 2-(2- oxo-1,2-dihydroindol-3-ylidene)malononitrile compound 12 with 3-methyl-1-phenyl-2- pyrazoline-5-one was carried out to give spiroindolopyranopyrazolo derivative 13. Compounds 4a,b was reacted with thioglycolic acid to give thiazolidinone derivatives 14a,b. Epoxidation of 5 using monoperoxyphthalic acid magnesium salt hexahydrate and hydrogen peroxide were executed to afford the novel dispiro (2-pyrazolin oxiraneindoline)dione compound 15. The chemical structures of the synthesized compounds were well established by elemental and spectral analyses.

Reactions of indole-2,3-dione 1 with 2-mercaptobenzimidazole, o-phenylenediamine, 2- aminophenol, 2-aminobenzothiazole, 2-aminobenzimidazole and 3-methyl-1-phenyl-2- pyrazolin-5-one were carried out to give compounds spiroindolethiazetobenzimidazole 2, spirobenzimidazole(oxazole)indoline 3a,b, benzothiazol(imidazol) iminoindolinone 4a,b and methyloxoindolylidenepyrazolone 5 respectively. Compound 5 was reacted with 2- aminophenol as well as o-phenylenediamine to give new spirooxazepine and diazepine derivatives 6a,b respectively. Reaction of 5 with nitrogen nucleophiles as well as carbon nucleophiles was investigated to furnish new spiro heterocycles 7-11. The reaction of 2-(2- oxo-1,2-dihydroindol-3-ylidene)malononitrile compound 12 with 3-methyl-1-phenyl-2- pyrazoline-5-one was carried out to give spiroindolopyranopyrazolo derivative 13. Compounds 4a,b was reacted with thioglycolic acid to give thiazolidinone derivatives 14a,b. Epoxidation of 5 using monoperoxyphthalic acid magnesium salt hexahydrate and hydrogen peroxide were executed to afford the novel dispiro (2-pyrazolin oxiraneindoline)dione compound 15. The chemical structures of the synthesized compounds were well established by elemental and spectral analyses.

In order to study effects of detergents at molecular level, we have done activity measurements of wheat germ lipase in increasing concentration of some commercial detergents. Conformational changes in protein structure using circular dichroism and fluorescence spectroscopy were studied in increasing concentration of sodium dodecyl sulfate. Our study proves that detergents may lead to loss of enzymatic activity and structure of plant enzymes. Since detergents are common source of pollution in water bodies and the water from these resources can be used in fields, our study may prove helpful in creating awareness about harmful action of detergents.

For two successive years, the floristic diversity and vegetation composition in the southern part of the Eastern Desert of Egypt were investigated through four transects (3 crossing the Eastern Desert and one along the Red Sea). The data collected from 142 stands covering the study area included the species composition, functional groups, chorologyand occurrences (Qvalues). A total of 94 plant species belonging to 33 different families were recorded, with Asteracea, Zygophyllaceae, Fabaceae, Poaceae, Chenopodiaceae and Brassicaceae as the largest families. Shrubs represented the largest functional group (39.4%),while perennial herbs represented the smallest ones(12.8%). Species occurrence (Q-value) revealed that Zilla spinosa, Acacia tortilis subsp. raddiana, Morettia philaeana, Caroxylon imbricatum, Zygophyllum coccineumandCitrullus colocynthis had wide ecological range of distribution (dominant species,Q-values ≥0.2). Saharo-Arabian chorotype was highly represented (72.6 %) in the flora of this area, eventually as mono, bi or pluriregional. Classification of the data set yielded 7 vegetation groups included: (A) Zilla spinosa-Morettia philaeana, (B1) Zilla spinosa-Citrullus colocynthis-Morettia philaeana,(B2)Zilla spinosa, (C1) Zygophyllum album-Tamarix nilotica, (C2) Zygophyllum coccineum-Tamarix nilotica, (D1) Zilla spinosa-Zygophyllum coccineum and (D2) Zilla spinosa-Acacia tortilis subsp. raddiana-Tamarix aphylla-Balanites aegyptiaca. Certain vegetation groups were assigned to one or more transects. Detrended Correspondence Analysis (DCA) revealed that electrical conductivity, sodium, potassium, calcium, magnesium, chlorides, moisture content, sulphates, pH, organic matter and gravel were the soil variables that affect the species distribution in this study.

For two successive years, the floristic diversity and vegetation composition in the southern part of the Eastern Desert of Egypt were investigated through four transects (3 crossing the Eastern Desert and one along the Red Sea). The data collected from 142 stands covering the study area included the species composition, functional groups, chorologyand occurrences (Qvalues). A total of 94 plant species belonging to 33 different families were recorded, with Asteracea, Zygophyllaceae, Fabaceae, Poaceae, Chenopodiaceae and Brassicaceae as the largest families. Shrubs represented the largest functional group (39.4%),while perennial herbs represented the smallest ones(12.8%). Species occurrence (Q-value) revealed that Zilla spinosa, Acacia tortilis subsp. raddiana, Morettia philaeana, Caroxylon imbricatum, Zygophyllum coccineumandCitrullus colocynthis had wide ecological range of distribution (dominant species,Q-values ≥0.2). Saharo-Arabian chorotype was highly represented (72.6 %) in the flora of this area, eventually as mono, bi or pluriregional. Classification of the data set yielded 7 vegetation groups included: (A) Zilla spinosa-Morettia philaeana, (B1) Zilla spinosa-Citrullus colocynthis-Morettia philaeana,(B2)Zilla spinosa, (C1) Zygophyllum album-Tamarix nilotica, (C2) Zygophyllum coccineum-Tamarix nilotica, (D1) Zilla spinosa-Zygophyllum coccineum and (D2) Zilla spinosa-Acacia tortilis subsp. raddiana-Tamarix aphylla-Balanites aegyptiaca. Certain vegetation groups were assigned to one or more transects. Detrended Correspondence Analysis (DCA) revealed that electrical conductivity, sodium, potassium, calcium, magnesium, chlorides, moisture content, sulphates, pH, organic matter and gravel were the soil variables that affect the species distribution in this study.

For two successive years, the floristic diversity and vegetation composition in the southern part of the Eastern Desert of Egypt were investigated through four transects (3 crossing the Eastern Desert and one along the Red Sea). The data collected from 142 stands covering the study area included the species composition, functional groups, chorologyand occurrences (Qvalues). A total of 94 plant species belonging to 33 different families were recorded, with Asteracea, Zygophyllaceae, Fabaceae, Poaceae, Chenopodiaceae and Brassicaceae as the largest families. Shrubs represented the largest functional group (39.4%),while perennial herbs represented the smallest ones(12.8%). Species occurrence (Q-value) revealed that Zilla spinosa, Acacia tortilis subsp. raddiana, Morettia philaeana, Caroxylon imbricatum, Zygophyllum coccineumandCitrullus colocynthis had wide ecological range of distribution (dominant species,Q-values ≥0.2). Saharo-Arabian chorotype was highly represented (72.6 %) in the flora of this area, eventually as mono, bi or pluriregional. Classification of the data set yielded 7 vegetation groups included: (A) Zilla spinosa-Morettia philaeana, (B1) Zilla spinosa-Citrullus colocynthis-Morettia philaeana,(B2)Zilla spinosa, (C1) Zygophyllum album-Tamarix nilotica, (C2) Zygophyllum coccineum-Tamarix nilotica, (D1) Zilla spinosa-Zygophyllum coccineum and (D2) Zilla spinosa-Acacia tortilis subsp. raddiana-Tamarix aphylla-Balanites aegyptiaca. Certain vegetation groups were assigned to one or more transects. Detrended Correspondence Analysis (DCA) revealed that electrical conductivity, sodium, potassium, calcium, magnesium, chlorides, moisture content, sulphates, pH, organic matter and gravel were the soil variables that affect the species distribution in this study.