142068-35-7

Upstream product

• 14850-96-5 acetophenone N-benzoylhydrazone 
• 14850-97-6 acetophenone N-benzoylhydrazone 
• 613-94-5 benzoic acid hydrazide 
• 98-86-2 acetophenone 
• 98-85-1 1-Phenylethanol 

Relevant academic research and scientific papers

Nickel-Catalyzed Asymmetric Hydrogenation of Hydrazones

An efficient nickel-catalyzed asymmetric hydrogenation of hydrazones to chiral hydrazines has been realized with up to 99 % yield and 99.4 : 0.6 er. Deuterium labelling experiments indicated that the hydrazone substrates undergo imine-enamine tautomerizat

Ruthenium-Catalyzed Enantioselective Hydrogenation of Hydrazones

Prochiral hydrazones undergo efficient and highly selective hydrogenation in the presence of a chiral diphosphine ruthenium catalyst, yielding enantioenriched hydrazine products (up to 99% ee). The mild reaction conditions and broad functional group tolerance of this method allow access to versatile chiral hydrazine building blocks containing aryl bromide, heteroaryl, alkyl, cycloalkyl, and ester substituents. This method was also demonstrated on >150 g scale, providing a valuable hydrazine intermediate en route to an active pharmaceutical ingredient.

Nickel-Catalyzed N-Alkylation of Acylhydrazines and Arylamines Using Alcohols and Enantioselective Examples

A borrowing-hydrogen reaction between amines and alcohols is an atom-economic way to prepare alkylamines, ideally with water as the sole byproduct. Herein, nickel catalysts are used for direct N-alkylation of hydrazides and arylamines using racemic alcohols. Moreover, a nickel catalyst of (S)-binapine was used for an asymmetric N-alkylation of benzohydrazide with racemic benzylic alcohols.

Nickel-Catalyzed Enantioselective Reductive Amination of Ketones with Both Arylamines and Benzhydrazide

An asymmetric reductive amination of ketones using both arylamines and benzhydrazide in the presence of nickel catalysts was developed. A one-pot synthesis of tetrahydroquinoxalines was also developed starting directly from α-ketoaldehydes and 1,2-diamino

RHODIUM CATALYST AND METHOD FOR PRODUCING AMINE COMPOUND

[Problem] Provision of a superior rhodium catalyst and a production method of amine compound. [Solving Means] A rhodium complex coordinated with a compound represented by the formula

Nickel-catalyzed asymmetric transfer hydrogenation of hydrazones and other ketimines

We report the use of nickel catalysts for the catalytic transfer hydrogenation of hydrazones and other ketimines with formic acid. Strongly donating bisphosphines must be used to support the catalysts. As in enzymatic catalysis, attractive weak interactio

Direct catalytic asymmetric reductive amination of simple aromatic ketones

A green method for chiral amine synthesis, the direct catalytic asymmetric reductive amination, was developed. Phenylhydrazide is an ideal nitrogen source for reductive amination. Molecular sieves play dual roles in this reaction. They help to remove Hsu

Novel phosphine ligands

The invention is concerned with new phosphine ligands of the formula I wherein R1 and R2 are independently of each other alkyl, aryl, cycloalkyl or heteroaryl, said alkyl, aryl, cycloalkyl or heteroaryl may be substituted by alkyl, alkoxy, halogen, hydroxy, amino, mono- or dialkylamino, aryl, —SO2—R7, —SO3?, —CO—NR8R8′, carboxy, alkoxycarbonyl, trialkylsilyl, diarylalkylsilyl, dialkylarylsilyl or triarylsilyl; R3 is alkyl, cycloalkyl, aryl or heteroaryl; R4′ and R4 signify independently of each other hydrogen, alkyl or optionally substituted aryl; or R4′ and R4 together with the C-atom they are attached to form a 3-8-membered carbocyclic ring; dotted line is absent or is present and forms a double bond; R5 and R6 are independently of each other hydrogen, alkyl or aryl; or linked together to form a 3-8-membered carbocyclic ring or an aromatic ring; R7 is alkyl, aryl or NR8R8′; and R8 and R8′ are independently of each other hydrogen, alkyl or aryl; metal complexes with such ligands as well as the use of such metal complexes as catalysts in asymmetric reactions.

Chiral diphosphinoterpenes and transition metal complexes thereof

The present invention relates to chiral diphosphinoterpenes and transition metal complexes thereof, to a process for preparing chiral diphosphinoterpenes and oxides thereof, and to transition metal complexes comprising the chiral diphosphinoterpenes. In a

Chiral diphosphorus compounds and their transition metal complexes

Chiral diphosphorus compounds (I) and their complexes with boranes are new. Chiral diphosphorus compounds of formula (I) and their complexes with boranes are new. *1-*3 : stereogenic C atom in R- or S- configuration; R 5>alkyl, arylalkyl or aryl; either R 1>-R 4>R 5> or 4-16C heterocyclic group; or R 1>+R 2> and/or R 3>+R 4>alkylene; R 6>R 5> or alkoxy; and n : 0-2. Independent claims are also included for the following: (1) phosphorus-containing cyclopentanol compounds of formula (IV); (2) phosphorus containing cyclopentane derivatives of formula (V) and (VI); (3) phosphorus containing cyclopentanol compounds of formula (VII) and their complexes with borane; (4) sulfur-containing cyclopentanol compounds of formula (IX); (5) the preparations of (I), (IV), (V), (VI), (VII) and (IX); (6) cyclopentanol compounds of formula (II); (7) transition metal complexes (C1) comprising (I); (8) catalysts (C2) comprising (C1); and (9) a method for preparing stereoisomerically enriched compounds in the presence of (C2). [Image] [Image].