A vest or belt is integrally formed with tubular, pet receiving passageways which extend around the wearer's body and terminate in pocket-like chambers for feeding and retrieval.
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| Number | Title | Issue Date |
| 7985857 | Usage 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 |
| 7358378 | Processes 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 |
| 7202370 | Semi-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 |
| 7115784 | Copper-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 |
| 6730782 | Carbamoyl substituted β-lactams Taxane derivatives having an amino substituted C13 side chain. ... | 05/04/2004 |
| 6569847 | Substituted 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 |
| 6562962 | Preparation 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 |
| 6225463 | Synthesis 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 |
| 6187916 | Process 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 |
| 6153747 | Process 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 |
| 6013791 | Process 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 |
| 6008347 | N-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 |
| 5916887 | 4-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 |
| 5866691 | Lactam 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 |
| 5831091 | Process 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 |
| 5808055 | Copper 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 |
| 5760219 | Pyridyl 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 |
| 5728827 | Process 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 |
| 5639878 | Acyloxylation 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 |
| 5629420 | Substituted 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 |
| 5606052 | Substituted 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 |
| 5574156 | ଲ-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 |
| 5567614 | Enzymatic 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 |
| 5563264 | Preparation 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 |
| 5554746 | Lactam 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 |
| 5440030 | Ru 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 |
| 5412092 | N-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 |
| 5386029 | Process 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 |
| 5334328 | Chiral 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 |
| 5317100 | Process 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 |
| 5312914 | Process 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 |
| 5300638 | Asymmetric 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 |
| 5288862 | Substituted 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 |
| 5286857 | Intermediate 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 |
| 5250677 | Azetidin-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 |
| 5229381 | Substituted 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 |
| 5204460 | Ruthenium 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 |
| 5202433 | Polysaccharide 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 |
| 5191077 | Diastereomeric 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 |
| 5191076 | Acetyloxylation 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 |