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Patent No. 5307162

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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Class 552/292 - Polycyclo ring system having the cyclohexadiene as one of the cyclos


Subclass of Class 552 - Organic compounds -- part of the class 532-570 series
Definition: Compounds wherein the cyclohexadiene is one of the cyclos
No. of patents: 39
Last issue date: 10/09/2007


NumberTitleIssue Date
7279502Polyamine 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
7253207Quinones 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
6967255Phenanthrene 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
6939896Cd45 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
6891072Process 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
6809176Quinones 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
6579994Process 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
6106994Production 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
58832704-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
5616734Process 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
5329026Process 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
5304658Quinone 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
4797357Light-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
4701245Oxidation 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
4678583Use 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
4670108Oxidation 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
4647349Oxidation 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
4639298Oxidation 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
4632782Oxidizing 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
4510090Method 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
4422972Novel 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
4394315Method 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
4302527Photoreactive 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
4215135Antiinflammatory 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
4198529Process 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
4132722Oxidative 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
4111967Silicon 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
4108908Oxidative 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
4101561Oxidative 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
4100203Oxidative 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
4100204Oxidative 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
4100205Oxidative 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
4100206Oxidative 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
4100202Oxidative 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
4098830Oxidative 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
4096190Oxidative 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
4085124Oxidative 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
4070383Oxidative 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
4067890Oxidative 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
 
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