Chiral carboxylic acid ligands derived from camphoric acid

Chiral carboxylic acid ligands derived from camphoric acid

Versatile and convenient preparations of chiral carboxylic acid ligands, derived from camphoric acid, are described, either by esterification of camphoric dichloride or by a regioselective opening of the corresponding anhydride by a variety of alcohols or diols.

Opis bibliograficzny
Główni autorzy:	Moloney, M, Paul, DR, Thompson, R, Wright, E
Format:	Journal article
Język:	English
Wydane:	1996

Podobne zapisy

Chiral heterocyclic ligands. XII. Metal complexes of a pyrazine ligand derived from camphor
od: Christopher M. Fitchett, i wsp.
Wydane: (2005-10-01)

SYNTHESIS OF CHIRAL 1,5-DIAMINES DERIVED FROM (R)-(+)-CAMPHOR
od: José E. D. Martins, i wsp.
Wydane: (2024-03-01)

Highly efficient resolution of racemic diethanolamine using chiral camphor-10-sulphonic acid
od: Neelima D. Tangellamudi, i wsp.
Wydane: (2005-01-01)

Strecker degradation of amino acids promoted by a camphor-derived sulfonamide
od: M. Fernanda N. N. Carvalho, i wsp.
Wydane: (2016-04-01)

Synthesis of camphor-derived chiral auxiliaries and their application in asymmetric Morita-Baylis-Hillman reactions
od: Lulama P. Mciteka, i wsp.
Wydane: (2016-09-01)

Chiral monophorous ligands derived from BINOL for asymmetric hydrogenation of α-dehydroamino acid derivatives
od: Meng Yang, i wsp.
Wydane: (2008-11-01)

Reactivity of Zinc Halide Complexes Containing Camphor-Derived Guanidine Ligands with Technical rac-Lactide
od: Angela Metz, i wsp.
Wydane: (2017-11-01)

Carboxylic acids and their derivatives [filem]
od: Open University
Wydane: (1971)

Carboxylic acids and their derivatives [kasetvideo]
od: Open University. An Algorithmic Approach to Computing Course Team
Wydane: (1971)

Enantioselective Recognition of Chiral Carboxylic Acids by a β-Amino Acid and 1,10-Phenanthroline Based Chiral Fluorescent Sensor
od: Yonghong Zhang, i wsp.
Wydane: (2015-05-01)

Efficient asymmetric addition of diethylzinc to ketones using tartaric acid derivative as chiral ligand
od: Ailing Hui, i wsp.
Wydane: (2007-12-01)

Ligand exchange and catalysis in phenylation reactions mediated by lead tetracarboxylates
od: Moloney, M, i wsp.
Wydane: (1998)

Palladium Catalysis: Dependence of the Efficiency of C–N Bond Formation on Carboxylate Ligand and Metal Carboxylate or Carboxylic Acid Additive
od: Jacques Muzart
Wydane: (2024-03-01)

Synthesis of carboxylic acids and its derivatives /
od: Nurul Syafiqa Abd. Rahman, 1988-, i wsp.
Wydane: (2011)

Catalytic asymmetric acetalization of carboxylic acids for access to chiral phthalidyl ester prodrugs
od: Liu, Yingguo, i wsp.
Wydane: (2019)

Catalytic asymmetric acetalization of carboxylic acids for access to chiral phthalidyl ester prodrugs
od: Yingguo Liu, i wsp.
Wydane: (2019-04-01)

Substituent effect of camphor sulfonamide ligand on the asymmetric addition of diethylzinc to aldehyde
od: Ai-Ling Hui, i wsp.
Wydane: (2006-08-01)

AMINO-ACID SYNTHESIS USING (L)-PYROGLUTAMIC ACID AS A CHIRAL STARTING MATERIAL
od: Baldwin, J, i wsp.
Wydane: (1989)

Erratum to: “Synthesis of fluorescent carboxylic acid ligands for construction of monolayers on nanostructures”
od: Jadhav Sushilkumar
Wydane: (2012-12-01)

Chiral Hydroxamic Acid Ligands in the Asymmetric Synthesis of Natural Products
od: Tushar Janardan Pawar, i wsp.
Wydane: (2023-12-01)

Pyrimidinone conjugates for the assignment of the absolute configuration of α-chiral carboxylic acids by 1H-NMR
od: Robert S. Murray, i wsp.
Wydane: (2002-03-01)

The influence of ligands in Pinhey phenylation reactions using lead(IV) tetracarboxylates
od: Moloney, M, i wsp.
Wydane: (1997)

Organotin(IV) complexes of carboxylic acid derivatives
od: Matela Garima, i wsp.
Wydane: (2012-02-01)

Synthesis of carboxylic acid derivatives of 2-pyrazolines
od: Albert Lévai, i wsp.
Wydane: (2007-05-01)

Carboxylic or the acid derivatives ; preparation and synthetic applications /
od: 242237 De Wolfe, Robert H.
Wydane: (1970)

Structural basis for ligand recognition and signaling of hydroxy-carboxylic acid receptor 2
od: Jae-Hyun Park, i wsp.
Wydane: (2023-11-01)

Properties of Camphorated Paramonochlorophenol and Camphorated Paramonochlorophenol Associated to Calcium Hydroxide
od: Halim NAGEM FILHO, i wsp.
Wydane: (2007-09-01)

(L)-PYROGLUTAMIC ACID AS A CHIRAL STARTING MATERIAL FOR ASYMMETRIC-SYNTHESIS
od: Baldwin, J, i wsp.
Wydane: (1991)

Spirocyclic systems derived from pyroglutamic acid.
od: Cowley, A, i wsp.
Wydane: (2011)

Synthesis of New Benzofuran-2-Carboxylic Acid Derivatives
od: M. Kowalewska, i wsp.
Wydane: (2013-01-01)

Beyond Kolbe and Hofer–Moest: Electrochemical Synthesis of Carboxylic Anhydrides from Carboxylic Acids
od: Dr. Andreas P. Häring, i wsp.
Wydane: (2022-05-01)

Saccharide-assisted resolution of bioactive chiral carboxylic acids via NHC-catalyzed regioselective transesterification
od: Dai, Shuolu, i wsp.
Wydane: (2024)

A Squaramide-Based Organocatalyst as a Novel Versatile Chiral Solvating Agent for Carboxylic Acids
od: Fabio Spiaggia, i wsp.
Wydane: (2024-05-01)

Acidity of Carboxylic Acid Ligands Influences the Formation of VO2(A) and VO2(B) Nanocrystals under Solvothermal Conditions
od: Brittney A. Beidelman, i wsp.
Wydane: (2023-06-01)

Pd-catalysed ligand-enabled carboxylate-directed highly regioselective arylation of aliphatic acids
od: Yan Zhu, i wsp.
Wydane: (2017-04-01)

Conformational and Supramolecular Aspects in Chirality of Flexible Camphor-Containing Schiff Base as an Inducer of Helical Liquid Crystals
od: Vladimir Burmistrov, i wsp.
Wydane: (2023-03-01)

Novel chiral skeletons for drug discovery: antibacterial tetramic acids.
od: Holloway, C, i wsp.
Wydane: (2011)

Chiral enantiopure bis(thio)ureas derived from TADDOL and their carboxylate complexation capacity
od: Gherase Dragos, i wsp.
Wydane: (2012-08-01)

Chiral Phosphoric Acid Diesters as Ligands in Asymmetric Transition Metal Catalyzed Hydrogenation
od: Manfred T. Reetz, i wsp.
Wydane: (2003-05-01)

CuH-Catalyzed Asymmetric Reduction of α,β-Unsaturated Carboxylic Acids to β-Chiral Aldehydes
od: Zhou, Yujing, i wsp.
Wydane: (2020)