Cloaking System Using Optoelectronically Controlled Camouflage
A Cloaking System designed to operate in the visible light spectrum, utilizes optoelectronics and/or photonic components to conceal an object within it.
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| Number | Title | Issue Date |
| 7279502 | Polyamine analog conjugates and quinone conjugates as therapies for cancers and prostate diseases Peptide conjugates in which cytocidal and cytostatic agents, such as polyamine analogs or naphthoquinones, are conjugated to a polypeptide recognized and cleaved by enzymes such as prostate-specific antigen (PSA) and cathepsin B are provided, as well as compositions... | 10/09/2007 |
| 7253207 | Quinones as disease therapies Novel quinones are provided, as well as compositions comprising these novel quinones. Methods of using the novel quinones in treatment of various indications including cancer are also provided. ... | 08/07/2007 |
| 6967255 | Phenanthrene compounds A phenanthrene compound represented by the formula (I): in which, R1, R2, R3, R4, R5, R6, R7, and R8 are identical or different and... | 11/22/2005 |
| 6939896 | Cd45 inhibitors Substituted naphthalenediones in accord with structural diagram (I): compositions thereof and methods for the use thereof, for the treatment of T cell mediated conditions such as autoimmune diseases and organ graft rejection. In compounds of the invention, wherein: ... | 09/06/2005 |
| 6891072 | Process for production of dimers or aromatic monohydroxyl compounds The present invention provides a method for preparing dimer of a monohydroxy aromatic compound. In the method of the present invention, oxidative coupling reaction of a monohydroxy aromatic compound represented by formula [I]: Ar—OH [I] | 05/10/2005 |
| 6809176 | Quinones as disease therapies Novel quinones are provided, as well as compositions comprising these novel quinones. Methods of using the novel quinones in treatment of various indications including cancer are also provided. ... | 10/26/2004 |
| 6579994 | Process for preparation of 2-Methyl-1,4-naphthoquinone The present invention describes a process for the preparation of 2-Methyl-1,4-naphthoquinone by oxidizing 2-methylnaphthalene with hydrogen peroxide in the presence of acetic acid.... | 06/17/2003 |
| 6106994 | Production process of polyphenol diesters, and positive photosensitive compositions A process for producing a polyphenol diester comprises esterifying a polyphenol compound and a naphthoquinone-1,2-diazidesulfonyl halide in the presence of for example monomethyldicyclohexylamine, and a positive photosensitive composition contains the res... | 08/22/2000 |
| 5883270 | 4-substituted-1, 2-naphthoquinones and their use in the inhibition of neoplastic cell growth Novel 4-substituted-1,2-naphthoquinones, pharmaceutical unit dosage forms containing 4-substituted-1,2-naphthoquinones, and uses of 4-substituted-1,2-naphthoquinones to inhibit the growth of cancer cells are disclosed.... | 03/16/1999 |
| 5616734 | Process for the catalytic oxidation of aromatic compounds The invention relates to the use of compounds of the formula I R1a Reb Oc (I), where a is from 1 to 6, b is from 1 to 4 and c is from 1 to 14 and the sum of a, b and c is in accordance with the... | 04/01/1997 |
| 5329026 | Process for preparation of 2-substituted 1,4-naphthoquinone A process for preparation of a 2-substituted-1,4-naphthoquinone which comprises oxidizing a 2-substituted naphthalene to obtain reaction products comprising a 2-substituted-1,4-naphthoquinone and a 6-substituted-1,4-naphthoquinone; adding a diene compound... | 07/12/1994 |
| 5304658 | Quinone derivatives, their production and use Quinone derivatives of the general formula: ##STR1## (wherein R1 and R2 are the same or different, and independently are a hydrogen atom or a methyl or methoxy group, or R1 and R2 combine with each other to... | 04/19/1994 |
| 4797357 | Light-stable reducible compounds and analytical compositions, elements and methods utilizing same Certain reducible aromatic and quinone compounds having bulky groups on the carbamate nitrogen atom have improved stability to light. These compounds are useful in analytical compositions, elements and methods, e.g. for assays of bacterial cells. These co... | 01/10/1989 |
| 4701245 | Oxidation of organic compounds using a catalyzed cerium (IV) composition A process for oxidizing aromatic and alkyl substituted aromatic compounds to quinonoid compounds by contacting an aromatic and alkyl aromatic compound with an acidic, aqueous solution of ceric oxidant in the presence of a catalytic amount of chromium cati... | 10/20/1987 |
| 4678583 | Use of hydrates for aqueous solution treatment A process for forming a purified solute from an aqueous solution is provided whereby a mixture of an extractant, a hydrate former and the aqueous solution is first formed. The hydrate former forms a hydrate with water while the solute does not form a hydr... | 07/07/1987 |
| 4670108 | Oxidation of organic compounds using ceric methanesulfonate in an aqueous organic solution A process for oxidizing aromatic and alkyl substituted aromatic compounds to carbonyl containing compounds by contacting an aromatic or alkyl aromatic compound with ceric methanesulfonate in an aqueous, weakly acidic solution containing an organic cosolve... | 06/02/1987 |
| 4647349 | Oxidation of organic compounds using ceric ions in aqueous trifluoromethanesulfonic acid A process for oxidizing aromatic and alkyl substituted aromatic compounds to carbonyl containing compounds by contacting an aromatic and alkyl aromatic compound with an aqueous solution of ceric trifluoromethanesulfonate having from at least 0.75 to 7 mol... | 03/03/1987 |
| 4639298 | Oxidation of organic compounds using ceric ions in aqueous methanesulfonic acid A process for oxidizing aromatic and alkyl substituted aromatic compounds to carbonyl containing compounds by contacting an aromatic and alkyl aromatic compound with an aqueous solution of ceric methanesulfonate having from at least 1.5 to 9 molar concent... | 01/27/1987 |
| 4632782 | Oxidizing an organic compound A process for oxidizing an organic compound by ceric sulfate dissolved in an aqueous sulfuric acid solution, wherein the organic compound is oxidized (1) by means of a ceric sulfate-aqueous sulfuric acid solution or a cerous sulfate-containing ceric sulfa... | 12/30/1986 |
| 4510090 | Method for the production of phenanthrenequinone Improvement of the yield and purity of phenanthrenequinone during its production by oxidation of phenanthrene by means of chromic acid in a sulfuric acidic medium is achieved by preparing a dispersion made up of phenanthrene, alkali dichromate and water a... | 04/09/1985 |
| 4422972 | Novel light-sensitive compounds and photoreactable compositions comprising same There are disclosed light-sensitive compounds and a composition comprising (a) such compounds and (b) a compound having at least one reactive site capable of stepwise photoreaction with the light-sensitive compounds. The light-sensitive compounds have the... | 12/27/1983 |
| 4394315 | Method for manufacturing p- and o-benzoquinone derivatives A method for synthesizing p- or o-benzoquinone derivatives represented by formula III or IV ##STR1## by oxidizing, with an aqueous hypohalite solution having a pH of from 8 to 10, a p- or o-hydroquinone derivative represented by formula I or II ... | 07/19/1983 |
| 4302527 | Photoreactive compositions comprising a light sensitive compound and another compound with reactive site There are disclosed light-sensitive compounds and a composition comprising (a) such compounds and (b) a compound having at least one reactive site capable of stepwise photo-reaction with the light-sensitive compounds. The light-sensitive compounds have th... | 11/24/1981 |
| 4215135 | Antiinflammatory 2-substituted-1H-phenanthro[9,10-d]imidazoles Certain 2-substituted-1H-phenanthro[9,10-d]-imidazoles such as 2-[(1,1,2,2-tetrafluoroethyl)-sulfonyl]-1H-phenanthro[9,10-d]imidazole, are useful as antiinflammatory agents.... | 07/29/1980 |
| 4198529 | Process for the production of alkoxy-substituted polycyclic aromatic compounds The invention provides a process for the production of alkoxy-substituted polycyclic aromatic compounds from corresponding hydroxy-substituted compounds.... | 04/15/1980 |
| 4132722 | Oxidative coupling of alkylphenols catalyzed by metal complexes of diimino acid Carbon-carbon coupled self-condensation products obtained by the oxidative coupling of alkylphenols are prepared by contacting an aqueous mixture of an alkyl phenol with oxygen in the presence of sufficient alkaline material to sustain a pH in the range o... | 01/02/1979 |
| 4111967 | Silicon containing catalysts Catalysts for the catalytic oxidation of organic compounds containing silicon, vanadium, sulfur, oxygen and at least one alkali metal element. The catalyst is prepared from a silicic acid which has an average particle size of less than 50 microns and an a... | 09/05/1978 |
| 4108908 | Oxidative coupling of alkylphenols or 1-naphthols catalyzed by metal complexes of thio-acid compounds Carbon-carbon coupled self-condensation products obtained by the oxidative coupling of alkylphenols or 1-naphthols are prepared by contacting an aqueous mixture of an alkylphenol or 1-naphthol with oxygen in the presence of sufficient alkaline material to... | 08/22/1978 |
| 4101561 | Oxidative coupling of alkylphenols catalyzed by metal complexes of imino acid compounds Carbon-carbon coupled self-condensation products obtained by the oxidative coupling of alkylphenols are prepared by contacting an aqueous mixture of an alkyl phenol with oxygen in the presence of sufficient alkaline material to sustain a pH in the range o... | 07/18/1978 |
| 4100203 | Oxidative coupling of alkylphenols or 1-naphthols catalyzed by metal complexes of an oxime of a keto or aldehyde compound Carbon-carbon coupled self-condensation products obtained by the oxidative coupling of alkylphenols or 1-naphthols are prepared by contacting an aqueous mixture of an alkylphenol or 1-naphthol with oxygen in the presence of sufficient alkaline material to... | 07/11/1978 |
| 4100204 | Oxidative coupling of alkylphenols or 1-naphthols catalyzed by metal complexes of a hydroxy- or keto-acid compound Carbon-carbon coupled self-condensation products obtained by the oxidative coupling of alkylphenols or 1-naphthols are prepared by contacting an aqueous mixture of an alkylphenol or 1-naphthol with oxygen in the presence of sufficient alkaline material to... | 07/11/1978 |
| 4100205 | Oxidative coupling of alkylphenols or 1-naphthols catalyzed by metal complexes of aminoketo compounds Carbon-carbon coupled self-condensation products obtained by the oxidative coupling of alkylphenols or 1-naphthols are prepared by contacting an aqueous mixture of an alkylphenol or 1-naphtol with oxygen in the presence of sufficient alkaline material to ... | 07/11/1978 |
| 4100206 | Oxidative coupling of alkylphenols or 1-naphthols catalyzed by metal complexes of keto alcohol compounds Carbon-carbon coupled self-condensation products obtained by the oxidative coupling of alkylphenols or 1-naphthols are prepared by contacting an aqueous mixture of an alkyl phenol or 1-naphthol with oxygen in the presence of sufficient alkaline material t... | 07/11/1978 |
| 4100202 | Oxidative coupling of alkylphenols or 1-naphthols catalyzed by cupric complexes Carbon-carbon coupled self-condensation products obtained by the oxidative coupling of alkylphenols or 1-naphthols are prepared by contacting an aqueous mixture of an alkylphenol or 1-naphthol with oxygen in the presence of sufficient alkaline material to... | 07/11/1978 |
| 4098830 | Oxidative coupling of alkylphenols or 1-naphthols catalyzed by metal complexes of dicarboxylic acid compounds Carbon-carbon coupled self-condensation products obtained by the oxidative coupling of alkylphenols or 1-naphthols are prepared by contacting an aqueous mixture of an alkylphenol, alkoxyphenyl, or 1-naphthol with oxygen in the presence of sufficient alkal... | 07/04/1978 |
| 4096190 | Oxidative coupling of alkylphenols catalyzed by metal ammonia complexes Carbon-carbon coupled self-condensation products obtained by the oxidative coupling of alkylphenols are prepared by contacting an aqueous mixture of an alkyl phenol with oxygen in the presence of sufficient alkaline material to sustain a pH in the range o... | 06/20/1978 |
| 4085124 | Oxidative coupling of alkylphenols, alkoxyphenols and 1-naphthols catalyzed by metal complexes of amino compounds Carbon-carbon coupled self-condensation products obtained by the oxidative coupling of alkylphenols, alkoxyphenols or 1-naphthols are prepared by contacting an aqueous mixture of the phenol or naphthol with oxygen in the presence of sufficient alkaline ma... | 04/18/1978 |
| 4070383 | Oxidative coupling of phenols and naphthols Self-condensation products obtained by the coupling of alkylphenols, alkoxyphenols or naphthols are prepared by contacting an aqueous mixture of the phenol or naphthol with oxygen or an oxygen-containing gas in the presence of a catalyst system comprising... | 01/24/1978 |
| 4067890 | Oxidative coupling of alkylphenols, alkoxyphenols and naphthols catalyzed by metal complexes of amino carboxylic and amino sulfonic acids Self-condensation products obtained by the oxidative coupling of certain alkylphenols, alkoxyphenols or naphthols are prepared by contacting an aqueous mixture of the phenol or naphthol with oxygen in the presence of a metal complex of an aminocarboxylic ... | 01/10/1978 |