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Class 540/357 - Having -C(=X)-, wherein X is chalcogen, bonded directly to the additional chalcogen


Subclass of Class 540 - Organic compounds -- part of the class 532-570 series
Definition: Compounds in which- - wherein X is chalcogen (i.e., oxygen,
No. of patents: 147
Last issue date: 07/26/2011


1        
NumberTitleIssue Date
7985857Usage of poly-3-hydroxybutyrates in preparation of β-lactam compounds
A method for preparing compounds having the formula(I) by using P(3HB), wherein R is R1, R2, R3 are lower linear or branched C1-C4...
07/26/2011
7358378Processes for the preparation of paclitaxel
The present invention provides processes for the production of paclitaxel. Paclitaxel is produced by protecting the C(7) and the C(10) hydroxy groups of 10-DAB with a bridging silicon-based protecting group. The resulting 7,10-protected 10-DAB derivative is then der...
04/15/2008
7202370Semi-synthesis of taxane intermediates from 9-dihydro-13-acetylbaccatin III
A method is provided for the semi-synthesis of taxane intermediates useful in the preparation of paclitaxel and docetaxel from 9-dihydro-13-acetylbaccatin III. The preparation of a suitably protected baccatin III backbone from 9-dihydro-13-acetylbaccatin III, and th...
04/10/2007
7115784Copper-catalyzed formation of carbon-heteroatom and carbon-carbon bonds
The present invention relates to copper-catalyzed carbon-heteroatom and carbon-carbon bond-forming methods. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between the nitrogen atom of an amide or a...
10/03/2006
6730782Carbamoyl substituted β-lactams
Taxane derivatives having an amino substituted C13 side chain. ...
05/04/2004
6569847Substituted azetidin-2-ones as cysteine protease inhibitors
This invention relates to substituted azetidin-2-ones and to pharmaceutical compositions containing such compounds. Their use in medicine as inhibitors of cysteine proteases, particularly the cathepsins is also described. The invention includes a compound...
05/27/2003
6562962Preparation of substituted isoserine esters using metal alkoxides and ଲ-lactams
A process for preparing N-acyl, N-sulfonyl and N-phosphoryl substituted isoserine esters in which a metal alkoxide is reacted with a ଲ-lactam....
05/13/2003
6225463Synthesis of new ଲ-lactams
The object of the present invention is the development of new chiral auxiliaries for improved ଲ-lactam formation that control both the diastereoselectivity of ଲ-lactam formation and which can be removed without destruction of the sensitive aze...
05/01/2001
6187916Process for the preparation of taxane derivatives and ଲ-lactam intermediates therefor
A process for the preparation of a taxane derivative of the formula ##STR1## in which R2 represents an RO--, RS-- or RR'N-- in which R represents an unsubstituted or substituted straight chain or branched alkyl, alkenyl or alkynyl, or cycloalky...
02/13/2001
6153747Process for the preparation of 2-halomethyl-penems and their use for the preparation of antibacterial penems
Process for the preparation of 2-halomethyl-penems (I) comprising (a) reacting an acetoxy-(protected hydroxyethyl)-2-azetidinone (III) with a 2-halothioacetic acid to form a 3-haloacetylthioazetidinone (V), (b) reacting (V) with oxalyl chloride to give an...
11/28/2000
6013791Process for the preparation of 4-(formylthio)-azetidin-2-one derivatives and penem derivatives
A process for the preparation of a compound of formula (IVA) which process comprises subjecting a compound of formula (V), where R is an ester-forming group or carboxy-protecting group, and X and Y are hydrogen or halogen provided that at least one of X o...
01/11/2000
6008347N-substituted 2-azetidinones
The present invention provides novel cis-N-iminomethyl-3,4-disubstituted-2-azetidinones, and their use in the preparation of N-acyl-2-azetidinones, intermediates in the semi-synthesis of taxol and taxol derivatives....
12/28/1999
59168874-substituted-3-(2-amino-2-cycloalkyl methyl)-acetamido azetidin-2-one derivatives as cysteine proteinase regulators
In accordance with the present invention, there are provided 4-substituted-3-(2-amino-2-cycloalkyl methyl)-acetamido azetidin-2-one derivatives of the formula: ##STR1## wherein n is 1, 2 or 3; in which R1, R2 and R3 a...
06/29/1999
5866691Lactam nucleic acids
Novel ଲ-lactam monomers bearing various functional groups are prepared. The novel ଲ-lactam monomers can be joined into oligomeric compounds such as via preferred phosphate linkages including phosphodiester and phosphorothioate linkages. Useful...
02/02/1999
5831091Process for preparing acetoxyazetidinone derivative and intermediate thereof
An N-›2-(1-hydroxyethyl)-3-oxopropyl!amine compound of the formula ›III!: ##STR1## wherein Ring B represents a benzene ring which may be substituted; W represents oxygen atom or sulfur atom; Y represents oxygen atom, sulfur atom or N R0,...
11/03/1998
5808055Copper catalyzed process for producing 4-substituted azetidinone derivatives
A process for producing a 4-substituted azetidinone derivative represented by the following general formula ›III!: ##STR1## (wherein OR is a protected hydroxy group, Y is an alkyl group, an alkoxy group, a silyloxy group, a carbamoyloxy group, an am...
09/15/1998
5760219Pyridyl substituted B-lactam compounds
Pyridyl substituted ଲ-lactam compounds used in preparing taxane derivatives having a 3' pyridyl substituted C13 side chain....
06/02/1998
5728827Process for the synthesis of azetidinones
This invention provides a process for preparing azetidinones useful as intermediates in the synthesis of penems and as hypocholesterolemic agents, particularly for azetidinones substituted in the C-3 and C-4 positions and optionally substituted at the rin...
03/17/1998
5639878Acyloxylation process for preparing 4-acyloxy-2-azetidinone derivatives
The present invention relates to a novel and improved process for preparing 4-acyloxy-2-azetidinone derivatives having the following formula (I) which are useful as an intermediate for synthesis of penem or carbapenem compounds: ##STR1## in whic...
06/17/1997
5629420Substituted acetoxyazetidinone derivatives and process for preparing 4-acyloxyazetidinone derivatives
A process for preparing a 4-acyloxyazetidinone or a derivative thereof represented by formula (IV): ##STR1## wherein R1 represents a hydrogen atom, a lower alkyl group, a hydroxyethyl group, or a protected hydroxyethyl group; R3...
05/13/1997
5606052Substituted acetoxyazetidinone derivatives and process for preparing 4-acyloxyazetidinone derivatives
A process for preparing a 4-acyloxyazetidinone or a derivative thereof represented by formula (IV): ##STR1## wherein R1 represents a hydrogen atom, a lower alkyl group, a hydroxyethyl group, or a protected hydroxyethyl group; R3...
02/25/1997
5574156ଲ-lactams used in preparing taxol
A ଲ-lactam of the formula: ##STR1## wherein R1 is aryl, substituted aryl, alkyl, alkenyl, or alkynyl; R2 is hydrogen, alkyl, acyl, acetal, ethoxyethyl, or other hydroxyl protecting group; and R3 is aryl, substit...
11/12/1996
5567614Enzymatic processes for resolution of enantiomeric mixtures of compounds useful as intermediates in the preparation of taxanes
Methods for the enzymatic resolution of mixtures of enantiomers, such as ଲ-lactam compounds, which may be employed as intermediates in the preparation of taxanes such as taxol, the latter useful in the pharmaceutical field....
10/22/1996
5563264Preparation of ଲlactam compounds
A process for preparing a ଲ-lactam compound of the formula (I): ##STR1## which comprises cyclization, in the presence of a catalyst, of an azetidinone derivative of the formula: ##STR2## is provided in which R1 is hydrogen, alky...
10/08/1996
5554746Lactam nucleic acids
Novel ଲ-lactam monomers bearing various functional groups are prepared. The novel ଲ-lactam monomers can be joined into oligomeric compounds such as via preferred phosphate linkages including phosphodiester and phosphorothioate linkages. Useful...
09/10/1996
5440030Ru catalyzed acyloxylation process for preparing 4-acyloxyazetidinone derivatives
A process for preparing a 4-acyloxyazetidinone or a derivative thereof represented by formula (IV): ##STR1## wherein R1 represents a hydrogen atom, a lower alkyl group, a hydroxyethyl group, or a protected hydroxyethyl group; R3...
08/08/1995
5412092N-substituted 2-azetidinones
Novel cis compound having the formula: ##STR1## wherein R1 is alkyl, haloalkyl, cycloalkyl, aryl or a carbohydrate derivative; X is O, N, S, C(O)O or a direct bond; and R2 is aryl, substituted aryl or heteroaryl are useful in th...
05/02/1995
5386029Process for the manufacture of 4-acyloxy-3-hydroxyethyl-azetidinones
The invention relates to a novel process for the manufacture of (3R,1'R)-4-acyloxy-3-(1'-hydroxyethyl)-2-azetidinones of formula ##STR1## in which R1 represents lower alkyl or aryl, by enantioselective reduction of the carbonyl group in a ...
01/31/1995
5334328Chiral azetidinone derivatives, and their use as dopes in liquid-crystal mixtures
Azetidinones of the formula I ##STR1## in which, for example, R1 is an alkyl or alkenyl radical, R2 and R3 are hydrogen or an alkyl or alkenyl radical, Z is hydrogen or (pseudo)halogen, A1, A2 an...
08/02/1994
5317100Process for the preparation of optically active acyloxyazetidinones
Compounds of the formula ##STR1## in which R1 is hydrogen or lower alkyl, R2 is hydrogen or a hydroxyl protective group R2 ' and R3 is substituted or unsubstituted phenyl or lower alkyl can be prepared in a...
05/31/1994
5312914Process for the manufacture of 4-acetoxy-3-hydroxyethyl-azetidinone
The invention relates to a novel process for the manufacture of 4-acetoxy-3-hydroxyethyl-azetidinone of the formula ##STR1## especially 4(R)-acetoxy-3(R)-(1'(R)-hydroxyethyl)-2-azetidinone, from enantiomerically pure compounds of the formula ##S...
05/17/1994
5300638Asymmetric synthesis of taxol side chain
The present invention relates to a process for the preparation of (3R, 4S)-3-hydroxy-4-phenyl-2-azetidinone derivatives which are useful intermediates in the synthesis of taxol from baccatin III, said process comprises reacting an acyloxyacetyl halide wit...
04/05/1994
5288862Substituted acetoxyazetidinone derivatives and process for preparing 4-acyloxyazetidinone derivatives
A process for preparing a 4-acyloxyazetidinone or a derivative thereof represented by formula (IV): ##STR1## wherein R1 represents a hydrogen atom, a lower alkyl group, a hydroxyethyl group, or a protected hydroxyethyl group; R3...
02/22/1994
5286857Intermediate for the preparation of penems
An efficient, multistep process for the synthesis of certain 6-(1-hydroxyethyl) 2-substituted penem antibiotics from 2-[4R-(triphenylmethylthio)-3S-(1R-(dimethyl-t-butylsilyloxy)ethyl)-2-azet idon-1-yl]acetic acid esters....
02/15/1994
5250677Azetidin-2-one derivatives as serine protease inhibitors
The present invention relates to new 3-guanidinoalkyl-2-azetidinones of the formula ##STR1## wherein: U and W can be the same or different and are selected from the group consisting of hydrogen and an amino protecting group; n is 1 to 3; X is a membe...
10/05/1993
5229381Substituted azetidinones as anti-inflammatory and antidegenerative agents
New substituted azetidinones of the general formula (A') which have been found to be potent elastase inhibitors and thereby useful anti-inflammatory and antidegenerative agents are described. ##STR1##...
07/20/1993
5204460Ruthenium catalyzed process for preparing 4-acetoxyazetidinones
A simplified process for preparing 4-acetoxyazetidinones of formula (I): ##STR1## wherein Z is a hydrogen atom, a lower alkyl group or a hydroxyethyl group which may or may not be protected is disclosed. According to the invention, azetidinones of fo...
04/20/1993
5202433Polysaccharide derivatives as separating agents
A polysaccharide derivative prepared by replacing a part or the whole of hydrogen atoms of hydroxyl and/or amino groups of a polysaccharide with one or more atomic groups represented by the following formula (1), (2) or (3) is new and useful for the separ...
04/13/1993
5191077Diastereomeric 5R,6S-6-(1R-hydroxyethyl)-2-(cis-1-oxo-3-thiolanylthio)-2-penem-3-carbox ylic acids
Diastereomeric 5R,6S-6-(1R-hydroxyethyl)-2-(1S-oxo-3R-thiolanylthio)-2-penem-3-carboxylic acid and 5R,6S-6-(1R-hydroxyethyl)-2-(1R-oxo-3S-thiolanylthio)-2-penem-3-carboxylic acid, and pharmaceutically-acceptable salts and in vivo hydrolyzable es...
03/02/1993
5191076Acetyloxylation process for producing 4-acetoxyazetidinones with osmium catalyst
A process for producing a 4-acetoxyazetidinone represented by formula (I): ##STR1## wherein Z represents a hydrogen atom, a lower alkyl group, or a protected or unprotected hydroxyethyl group; and W represents a hydrogen atom, a lower alkyl group, or...
03/02/1993
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