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A space-saving dishwasher, which may be installed within a counter top or table, having a dish-carrying rack that is vertically shiftable through the open top of the dishwasher for facilitating loading and unloading of the dishes.

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Class 549/459 - Two of the cyclos share at least three ring members (i.e., bridged)


Subclass of Class 549 - Organic compounds -- part of the class 532-570 series
Definition: Compounds wherein at least three ring members of one cyclo
No. of patents: 55
Last issue date: 01/29/2008


1    
NumberTitleIssue Date
7323604Hydride reduction of α,β-unsaturated carbonyl compounds using chiral organic catalysts
Nonmetallic, chiral organic catalysts are used to catalyze the 1,4-hydride reduction of an α,β-unsaturated carbonyl compound. The α,β-unsaturated carbonyl compound may be an aldehyde or cyclic ketone, and the hydride donor may be a dihydropyridine. The reaction ...
01/29/2008
7173139Enantioselective 1,4-addition of aromatic nucleophiles to α,β-unsaturated aldehydes using chiral organic catalysts
Nonmetallic, chiral organic catalysts are used to catalyze the 1,4-addition of an aromatic nucleophile to an α,β-unsaturated aldehyde. The aromatic nucleophile may be an N,N-disubstituted aniline compound, or an analog thereof. The reaction is efficient and enanti...
02/06/2007
6797832Process for the production of 5-oxy-7-oxabicyclo [4.1.0] hept-3-ene-3-carboxylic acid esters
The present invention provides a method of producing 5-oxy-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylic acid ester economically, industrially advantageously and efficiently in a large amount. The present invention is a method of producing 5-oxy-7-oxabicyclo[4.1.0]hept...
09/28/2004
6559347Diels-adler adducts of epoxybutene and epoxybutene derivatives
Diels-Alder adducts of dienophiles such as epoxybutene with dienes such as cyclopentadiene and cyclohexadiene are produced by carrying out the Diels-Alder reaction thereof at an elevated pressure. Addional dienophiles disclosed include 2,5-dihydrofuran an...
05/06/2003
6555697Method of preparing a benzofuran or benzothiophene compound
The invention concerns a novel method for preparing a benzofuran or benzothiophene compound by cyclizing an aromatic compound bearing a side-chain comprising at least two carbon atoms, one of the carbon atoms being bound to the benzene cycle by an oxygen ...
04/29/2003
6515137Catalytic processes employing chiral imidazolidinone-based catalyst composition
Acid addition salts of imidazolidinones are provided as catalysts for transforming a functional group within a first reactant by reaction with a second reactant. Exemplary first reactants are ଱,ଲ-unsaturated carbonyl compounds such as ଱,...
02/04/2003
6486201Agarofuan derivatives, their preparation, pharmaceutical composition containing them and their use as medicine
The compound represented by formula (I), in which the substitutes are defined as in the specification and the claims, or their stereoisomers, the process for preparing them, pharmaceutical composition containing them and their use as medicine. ##STR1...
11/26/2002
6369243Chemical transformation of substrates using nonmetallic, organic catalyst compositions
A method is provided for catalytically transforming a functional group within a first reactant by reaction with a second reactant in the presence of a nonmetallic, organic catalyst composition composed of a heteroatom-containing activator and an acid, or ...
04/09/2002
635915218-substituted-19-nor-vitamin D compounds
This invention provides a novel class of vitamin D compounds, namely, 13-ethyl and 13-vinyl-18,19-dinor-vitamin D derivatives, as well as a general method for their chemical synthesis. The compounds have the formula: ##STR1## where Y1 and ...
03/19/2002
6252093Total synthesis of antitumor acylfulvenes
A compound of formula (IV): ##STR1## wherein R' and R9 are each independently (C1 -C4)alkyl....
06/26/2001
6103940Preparation of zeaxanthin, intermediates for this preparation, and the preparation thereof
Preparing (3R, 3'R)-zeaxanthin of the formula I ##STR1## starting from (4-hydroxy-2,2,6-trimethylcyclohexanone of the formula II ##STR2## via the novel intermediates (4R,6R)-1-formyl-2,2,6-trimethyl-7-oxabicyclo[2.2.1]heptane of the formula ...
08/15/2000
6077864Cyclic sulfone derivatives
A compound of the formula ##STR1## wherein n, X, Y and Ar are as defined herein, useful in the treatment of a condition selected from the group consisting of arthritis, cancer, tissue ulceration, macular degeneration, restenosis, periodontal disease,...
06/20/2000
5990104Polycyclic alcaloid-derivatives as NMDA-receptor antagonists
Polycyclic alkaloids of formula (I), wherein R1 is H, C1-6 alkyl, or C6-12 aryl optionally substituted with polar groups; R2 and R3 are independently H, OH, C1-6 alkyl, --C(NH)--NH2, ...
11/23/1999
5728846Benzo›1,2-g!-chrom-3-ene and benzo›1,2-g!-thiochrom-3-ene derivatives
Compounds of the formula ##STR1## where the symbols have the meaning defined in the specification, have retinoid, retinoid antagonist and/or retinoid inverse-agonist-like biological activity....
03/17/1998
5422365Naphthalene compounds
A compound selected from those of formula (I): ##STR1## wherein: R1, R'1 and R2 are each selected, independently of the others, from hydrogen and an alkyl radical, the two R2 groups being in the cis positio...
06/06/1995
5344942Reagents for racmate resolution
(R) and (S) enantiomers of the formula ##STR1## in which n is 1 or 2, W is as defined in the specification which are characterized in that X is halogen, SO3 H, SO2 Cl or SO2 NR1 R2 where R1...
09/06/1994
5338758Bicyclic diterpene PAF antagonist compounds
Four bicyclic terpenes isolated from a culture broth of Phoma sp SCF0592, ATCC 74077, pharmaceutical compositions containing them and their use as PAF antagonists to treat allergic and inflammatory diseases are disclosed....
08/16/1994
5276053Polycyclic amines useful as cerebrovascular agents
A novel series of polycyclic amines, derivatives, methods of making the compounds, novel intermediates, compositions containing them, and methods for using them in the treatment and prevention of cerebrovascular disorders are disclosed....
01/04/1994
5175314Herbicidal oxatricyclic ethers
This invention relates to certain herbicidal oxatricyclic ethers, agriculturally suitable compositions thereof and a method for their use as broad spectrum preemergent or postemergent herbicides....
12/29/1992
5084581Process for preparing (3R-(3a଱,4ଲ,7ଲଲ,7a଱))-octahydro-4,7 epoxyisobenzofuranol from associated aldehydes
Disclosed herein is a novel process in which novel aldehydes ##STR1## and the trans isomer thereof are hydrolyzed by treatment with an alkali metal carbonate, bicarbonate or hydroxide and water to form the cis enantiomer ##STR2## Also discl...
01/28/1992
5071853Polycyclic amines useful as cerebrovascular agents
A novel series of polycyclic amines, derivatives, methods of making the compounds, novel intermediates, compositions containing them, and methods for using them in the treatment and prevention of cerebrovascular disorders are disclosed....
12/10/1991
4956481Adamantane derivatives, compositions of matter containing same, processes for preparing said adamantane derivatives and said compositions, and organoleptic and deodorancy uses of said adamantane derivatives and said compositions
Described are hydroxy adamantane compounds and derivatives thereof and a process for preparing same....
09/11/1990
4935532Hemiacetals
All possible isomeric forms of a compound of the formula ##STR1## wherein A has a structure selected from the group consisting of ##STR2## wherein Y1 and Y2 are individually selected from the group consisting of hydrogen, f...
06/19/1990
4855426Process of preparing 1,5-epoxy-2,3,4,5-tetrahydro-1H-3-benzazepins
The synthesis of epoxybenzazepin compounds is described. The novel compounds have anti-ulcer activity....
08/08/1989
4788305Novel resolution process
Compounds of the formula ##STR1## wherein A is a hydrocarbon chain containing 1 to 16 groups, the said chain containing at least one heteroatom, at least one unsaturation, the assembly of the group constituting the chain may be a mono- or polycyclic ...
11/29/1988
47821694,7-dioxatricyclo(3.2.1.03,6)octane ether
Compounds of the Formula I, II, III, VI and VII ##STR1## wherein the symbols have defined meanings are herbicides, plant growth regulators or intermediates thereof....
11/01/1988
4739082Enantiomerically pure mono acetal-protected diols, their preparation and use
Enantiomerically pure mono acetal-protected diols of the formula ##STR1## wherein A, B, C and D are hydrogen or a methyl group in any combination, M and N are aliphatic or araliphatic hydrocarbons, m and n are the numbers 0, 1 or 2, whereby the total...
04/19/1988
47344265,6-epoxy-7-oxabicycloheptane substituted diamide prostaglandin analogs
5,6-Epoxy-7-oxabicycloheptane substituted diamide prostaglandin analogs are provided having the structural formula ##STR1## wherein A is --CH.dbd.CH-- or --CH2 --CH2 --; n is 1 to 5; R is CO2 H, CO2 alkyl, ...
03/29/1988
4701542Resolution of hemiacetals and alcohols
A process for the resolution of hemiacetal compounds of the formula ##STR1## wherein A is a hydrocarbon chain containing 1 to 16 groups, the said chain optionally containing at least one heteroatom, at least one unsaturation, the assembly of the grou...
10/20/1987
4670041Oxabicycloalkane herbicides
Compounds of the formula ##STR1## wherein X is (--CR4 R4 --)m in which m is 0 or 1; Y is (--CR5 R6 --)n in which n is 0, 1 or 2; Z is (--CR7 R7 --)p in which p i...
06/02/1987
46110065,6-epoxy-7-oxabicycloheptane substituted ethers useful in the treatment of thrombotic disease
5,6-Epoxy-7-oxabicycloheptane substituted ether prostaglandin analogs are provided having the structural formula ##STR1## wherein X is O or ##STR2## and including all stereoisomers thereof. The compounds are cardiovascular agents useful, fo...
09/09/1986
46110055,6-epoxy-7-oxabicycloheptane substituted prostaglandin analogs useful in the treatment of thrombotic disease
5,6-Epoxy-7-oxabicycloheptane substituted prostaglandin analogs are provided having the structural formula ##STR1## wherein m is 1 to 5, R is H, lower alkyl, alkali metal or polyhydroxylamine, and R1 is lower alkyl, aryl, aralkyl, cycloalk...
09/09/1986
46096715,6-epoxy-7-oxabicycloheptane substituted amino prostaglandin analogs useful in the treatment of thrombotic disease
5-6-Epoxy-7-oxabicycloheptane substituted amino prostaglandin analogs are provided having the structural formula ##STR1## wherein A is CH.dbd.CH or (CH2)2, m is 1 to 8, n is 0 to 5, R is H, lower alkyl, alkali metal or hydroxyla...
09/02/1986
4554366Certain substituted, 7-oxabicyclo[2.2.1]heptan-2-ols and -2-ones as intermediates
Compounds of the formula ##STR1## wherein X is (--CR4 R4 --)m in which m is 0 or 1; Y is (--CR5 R6 --)n in which n is 0, 1 or 2; Z is (--CR7 R7 --)p in which p i...
11/19/1985
45032417-Oxabicycloheptane prostaglandin intermediates
7-Oxabicycloheptane prostaglandin intermediates are provided having the general structure ##STR1## wherein one of R1 and R2 is ##STR2## and the other is hydrogen. A method for preparing the above intermediates is also ...
03/05/1985
4500543Substituted 1-aminomethyl-phthalans
Disclosed herein are 1-aminomethyl-phthalans represented by the formula ##STR1## wherein R, R1, and R2 are independently selected from hydrogen, hydroxy, loweralkoxy of 1 to 3 carbon atoms, loweralkenyloxy of 1 to 3 carbon atoms...
02/19/1985
45007237-Oxabicycloheptaine prostaglandin intermediates and method for preparing same
7-Oxabicycloheptane prostaglandin intermediates are provided having the general structure ##STR1## wherein one of R1 and R2 is ##STR2## and the other is hydrogen. A method for preparing the above intermediates is also ...
02/19/1985
44992927-Oxabicycloheptane prostaglandin intermediates and method for preparing same
Optically active 7-oxabicyclopheptane prostaglandin intermediates are provided having the general structure ##STR1## wherein one of R1 and R2 is ##STR2## and the other is hydrogen. A method for preparing the above intermedi...
02/12/1985
4497960Chiral, optically active compounds useful as protective groups for hydroxy, thiol and amino compounds
The invention declares new chiral, optically active compounds of the general formula ##STR1## wherein a 5 or 6 membered lactol ring (E), with X and Y meaning (CR1 R2)n, with n=0 to 2 and R1, R2 =...
02/05/1985
44862206-Oxatricyclo[3.2.1.13,8 ]nonan-4-ol ethers and compositions and methods for the regulation of plant growth
Compounds of the formula ##STR1## wherein each R is H or alkyl and W is an optionally substituted unsaturated group, a cycloalkyl group, a secondary alkyl group, an aromatic group or a heterocyclic group, are useful as plant growth regulators an...
12/04/1984
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