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| Number | Title | Issue Date |
| 6008414 | Dioxane-monochloroborane and dioxane-dichloroborane Highly reactive hydroborating agents dioxane-monochloroborane and dioxane-dichloroborane are provided. Also provided by this invention are methods for producing dioxane-monochloroborane, dioxane-dichloroborane and methods for hydroborating olefins with th... | 12/28/1999 |
| 5567849 | Borane-sulfide hydroboration agents A borane-sulfide represented by the formula BH3.SR1 R2 wherein B is boron, H is hydrogen, R1 and R2 each are straight or branched chain alkyl or alkoxy with at least one R being a branched chain when both ... | 10/22/1996 |
| 5552081 | Dicyclooctylhaloboranes A novel class of enolboration reagents represented by the formula R2 BX/R'3 N wherein each R is the same or different alkyl or cycloalkyl, B is boron, X is halo, R' is lower alkyl and/indicates that R2 BX is preferably employed... | 09/03/1996 |
| 5543569 | Borane-N,N-dialkylaniline hydroboration agents Borane-N,N-dialkylanilines represented by the formula H3 B. C6 H5 NRR' wherein N is nitrogen, R is isobutyl or isopropyl and R' is straight or branched chain lower alkyl. The compounds are useful as hydroboration agents and for... | 08/06/1996 |
| 5504240 | Borane-hydroxydialkylsulfide borates Novel borane adducts of hydroxydialkylsulfide borate esters represented by formula ##STR1## wherein R is straight or branched chain alkyl or alkoxy having from 2 to 5 carbon atoms and n is 1 to 3 inclusive. The compound are new hydroboration age... | 04/02/1996 |
| 5481038 | Borane-N,N-diisopropylalkylamine hydroboration agents Borane-N,N-diisopropylalkylamines as represented by the formula: H3 B.NPri2 R wherein Pri is isopropyl, R is branched-chain alkyl or cycloalkyl having 3 to 6 carbon atoms and B is boron are provided. The compounds are ... | 01/02/1996 |
| 5380940 | Bis(bicyclo(2.2.2)octyl)haloboranes A novel class of enolboration reagents represented by the formula R2 BX/R'3 N wherein each R is the same or different alkyl or cycloalkyl, B is boron, X is halo, R' is lower alkyl and / indicates that R2 BX is preferably employ... | 01/10/1995 |
| 5284976 | Method of producing primary amines in high yields A novel process for producing hindered and unhindered primary amines represented by the formula RNH2 and R*NH2 in high yields from novel intermediates RBMe2 or R*BMe2 wherein R is an organo group, R* is a chiral... | 02/08/1994 |
| 5276195 | Process for producing dimethylorganoboranes A process for preparing a dimethylorganoborane represented by the formula R*BMe2 wherein R* is a chiral organyl group attached to the boron, B is boron and Me is methyl comprising treating a chiral boronic ester R*B(OR')2 with a meth... | 01/04/1994 |
| 5220072 | Process of synthesizing chemically and optically pure B-halodiiso-2-ethylapopinocampheylboranes A chemically and optically pure B-halodiiso-2-ethylapopinocampheylborane of essentially 100% ee represented by the formula: ##STR1## wherein B is borane and X is halo and a process for preparing.... | 06/15/1993 |
| 5214209 | Method of producing primary amines in high yields and novel intermediates therefor A novel process for producing hindered and unhindered primary amines represented by the formula RNH2 and R*NH2 in high yields from novel intermediates RBMe2 or R*BMe2 wherein R is an organo group, R* is a chiral... | 05/25/1993 |
| 5210310 | Optically active dimethylorganoboranes A novel process for producing hindered and unhindered primary amines represented by the formula RNH2 and R*NH2 in high yields from novel intermediates RBMe2 or R*BMe2 wherein R is an organo group, R* is a chiral... | 05/11/1993 |
| 5202502 | Process for producing optically active alcohols A chemically and optically pure B-halodiiso-2-ethylapopinocampheylborane of essentially 100% ee represented by the formula: ##STR1## wherein B is borane and X is halo, and a process of using such for the production of optically active alcohols.... | 04/13/1993 |
| 5175378 | Synthesis of optically pure forms of ipsdienol An improved process for preparing either optically pure enantiomer of the bark beetle pheromones ipsenol and ipsdienol is provided. The process is also applicable to the condensation of aldehydes of widely varying properties to the corresponding chiral al... | 12/29/1992 |
| 5175371 | Synthesis of optically pure forms of ipsenol An improved process for preparing either optically pure enantiomer of the bark beetle pheromones ipsenol and ipsdienol is provided. The process is also applicable to the condensation of aldehydes of widely varying properties to the corresponding chiral al... | 12/29/1992 |
| 5159116 | Chemically and optically pure B-halodiiso-2-ethylapopinocampheylboranes A chemically and optically pure B-halodiiso-2-ethylapopinocampheylborane of essentially 100% ee represented by ##STR1## wherein B is borane and X is halo.... | 10/27/1992 |
| 5103063 | Intermediates useful for the chiral isoprenylation of aldehydes An improved process for preparing either optically pure enantiomer of the bark beetle pheromones ipsenol and ipsdienol is provided. The process is also applicable to the condensation of aldehydes of widely varying properties to the corresponding chiral al... | 04/07/1992 |
| 5087700 | Method of producing primary amines in high yields A novel process for producing hindered and unhindered primary amines represented by the formula RNH2 and R*NH2 in high yields from novel intermediates RBMe2 or R*BMe2 wherein R is an organo group, R* is a chiral... | 02/11/1992 |
| 5068432 | Process for producing optically pure 2-phenoxyphenylalkylamines A process for producing the optically pure (+)- or (-) isomer of a phenyl- or substituted- phenylalkanolamine compounds having pharmacologic activity without the need for resolution processes and novel intermediates useful in the process including optical... | 11/26/1991 |
| 5043479 | Chemically and optically pure diisopinocampheylhaloboranes Novel chemically pure diisopinocampheylhaloboranes of essentially 100% ee, represented by the formula Ipc2 BX wherein Ipc is isopinocampheyl and X is halo.... | 08/27/1991 |
| 4978794 | Novel ଲ-(2-alkenyl)bis(2-isocaranyl)boranes 2-Alkenylbis(2-isocaranyl)boranes represented by the formula: ##STR1## wherein R is 2-alkenyl. The compounds undergo asymmetric 2-alkenylboration with a variety of aldehydes and afford the corresponding alcohols in 94-99% ee.... | 12/18/1990 |
| 4918242 | Novel optically 1,3-phenoxypropylhalides A process for producing the optically pure (+)- or (-)-isomer of a phenyl- or substituted-phenylalkanolamine compounds having pharmacologic activity without the need for resolution processes and novel intermediates useful in the process including opticall... | 04/17/1990 |
| 4918246 | Process for preparing optically active haloalcohols A process for producing the optically pure (+)- or (-) isomer of a phenyl- or substituted- phenylalkanolamine compounds having pharmacologic activity without the need for resolution processes and novel intermediates useful in the process including optical... | 04/17/1990 |
| 4918207 | Novel optically active halo-substituted tetrahydrofurans A process for producing the optically pure (+)- or (-) isomer of a pheynl- or substituted- phenylalkanolamine compounds having pharmacologic activity without the need for resolution processes and novel intermediates useful in the process including optical... | 04/17/1990 |
| 4918229 | Method of producing primary amines in high yields and novel intermediates therefor A novel process for producing hindered and unhindered primary amines represented by the formula RNH2 and R*NH2 in high yields from novel intermediates RBMe2 or R*BMBe2 wherein R is an organo group, R* is a chira... | 04/17/1990 |
