| Class / Patent application number | Description | Number of patent applications / Date published |
|---|
| 560020000 | Nitro bonded to carbon in acid moiety | 11 |
| 20140275603 | PROCESS FOR MAKING 2-NITRO-1-ETHANOL DERIVATIVES - A process for making a 2-nitro-1-ethanol derivative of formula III: wherein R3 is as described herein is provided. Novel 2-nitro-1-ethanol derivatives provided. | 09-18-2014 |
| 560021000 | Plural rings in acid moiety | 6 |
| 20090023943 | Synthesis Reaction Catalyst and Method of Synthesizing Compound Using the Same - To improve a catalytic activity of a composite oxide, to carry out a reaction in a high yield, and to provide a synthesis reaction catalyst having excellent handling properties and a method of a synthesizing a compound using the same, a synthesis reaction catalyst containing a palladium-containing perovskite-type composite oxide having a specific surface area of 0.5 to 9.5 m | 01-22-2009 |
| 20100081838 | Cobalt-Catalyzed Asymmetric Cyclopropanation of Alkenes with alpha-Nitrodiazoacetates - A process for the cyclopropanation of olefins with a metal porphyrin catalyst and an acceptor/acceptor substituted diazo reagent. | 04-01-2010 |
| 20130096338 | ASYMMETRIC CYCLIZATION PROCESSES USING UNSATURATED NITRO COMPOUNDS - Disclosed are processes of forming a compound (33), (35) or (37) | 04-18-2013 |
| 20130345465 | PROCESS FOR THE PREPARATION OF RETIGABINE - This invention relates to a novel chemical process for the synthesis of 2-ethyoxycarbonylamino-5-(4-fluorobenzylamino)-nitrobenzene and its use in the preparation of 2-amino-4-(4-fluorobenzylamino)-1-ethoxycarbonylaminobenzene (retigabine/ezogabine) and its polymorphic forms thereof. | 12-26-2013 |
| 20140135519 | CARBOXYLIC ACID ESTER PRODRUG INHIBITORS OF MEK - The invention generally relates to compounds having structure I: | 05-15-2014 |
| 20180022690 | PROCESS AND INTERMEDIATES FOR THE PREPARATION OF NEP INHIBITORS | 01-25-2018 |
| 560022000 | Additional nitrogen in acid moiety | 3 |
| 20100217028 | PROCESS FOR PREPARING NITROOXYALKYL SUBSTITUTED ESTERS OF CARBOXYLIC ACIDS, INTERMEDIATES USEFUL IN SAID PROCESS AND PREPARATION THEREOF - The present invention refers to a process for preparing a compound of general formula (A), as reported in the description, wherein R is a radical of a drug and R1-R12 are hydrogen or alkyl groups, m, n, o, q, r and s are each independently an integer from 0 to 6, and p is 0 or 1, and X is O, S, SO, SO2, NR13 or PR13 or an aryl, heteroaryl group, said process comprising reacting a compound of formula (B) R—COOZ (B) wherein R is as defined above and Z is hydrogen or a cation selected from: Li+, Na+, K+, Ca++, Mg++, tetralkylammonium, tetralkylphosphonium, with a compound of formula (C), as reported in the description, wherein R1-R12 and m, n, o, p, q, r, s are as defined above and Y is a suitable leaving group. | 08-26-2010 |
| 20130197259 | ANTIPROLIFERATIVE COMPOUNDS, CONJUGATES THEREOF, METHODS THEREFOR, AND USES THEREOF - Antiproliferative compounds having a structure represented by formula (II), where n, R | 08-01-2013 |
| 20140163252 | PROCESS FOR THE PREPARATION OF AN ANTICONVULSANT COMPOUND - The invention provides a novel method for the preparation of intermediates useful in a process designed to obtain known 1,2,4-triaminobenzene compounds, and in particular a specific compound thereof having known anticonvulsant activity. Unlike known methods, the novel method does not require advance protection of the amino groups present on the substrate. | 06-12-2014 |
| 560023000 | Oxy, aldehyde or ketone group in acid moiety | 1 |
| 20130053598 | METHOD FOR PRODUCING A CROSS-COUPLING PRODUCT OF A BENZENOID DIAZONIUM SALT - The invention relates to a method for producing a cross-coupling product of a benzenoid dizonium salt according to the general formula (I), wherein the groups R | 02-28-2013 |
