Results 41 to 50 of about 66,085 (162)

Stereoselective Synthesis of α-Amino-C-phosphinic Acids and Derivatives

open access: yesMolecules, 2016
α-Amino-C-phosphinic acids and derivatives are an important group of compounds of synthetic and medicinal interest and particular attention has been dedicated to their stereoselective synthesis in recent years. Among these, phosphinic pseudopeptides have
José Luis Viveros-Ceballos   +3 more
doaj   +1 more source

Meat and cancer: haemoglobin and haemin in a low calcium diet promote colorectal carcinogenesis at the aberrant crypt stage in rats [PDF]

open access: yes, 2003
High intake of red meat, but not of white meat, is associated with an increased risk of colon cancer. However, red meat does not promote cancer in rodents.
Corpet, Denis E.   +4 more
core   +5 more sources

Copper-Catalyzed Asymmetric Carboboronation of Allenes to Access α-Quaternary Amino Esters with Adjacent Stereocenters

open access: yesCell Reports Physical Science, 2020
Summary: Optically active α-quaternary amino acids have received much attention because of the important biomedical applications implicated for compounds containing this structure.
Chao-Yang Zhao   +5 more
doaj   +1 more source

Asymmetric Reduction of Lactam-based β-Aminoacrylates. Synthesis of Heterocyclic β2-Amino Acids [PDF]

open access: yes, 2016
The ability to affect asymmetric reduction of heterocyclic β-aminoacrylates 1 (n = 1–3) has been assessed with pyrrolidine and piperidone variants generating the corresponding N-heterocyclic β2-amino acids 3b and 5b with high enantioselectivity (≥97% ee)
Gallagher, Timothy   +4 more
core   +2 more sources

Gold amides as anticancer drugs: synthesis and activity studies [PDF]

open access: yes, 2013
Modular gold amide chemotherapeutics: Access to modern chemotherapeutics with robust and flexible synthetic routes that are amenable to extensive customisation is a key requirement in drug synthesis and discovery.
Amagai   +34 more
core   +1 more source

Beyond Peptides and Peptidomimetics: Natural Heteroaromatic Amino Acids in the Synthesis of Fused Heterocyclic Frameworks for Bioactive Agents

open access: yesOrganics
Heterocycle cores are widely used in medicinal chemistry for developing bioactive compounds. In this scenario, using cheap and accessible starting material to build these heterocycles is desirable to obtain new drug candidates for cost-efficient ...
Isis Apolo Silveira de Borba   +3 more
doaj   +1 more source

N,N’-Substituted 1,2,5 Thiadiazolidine 1,1-Dioxides: Synthesis, Selected Chemical and Spectral Proprieties and Antimicrobial Evaluation â€

open access: yesMolecules, 2005
The sulfamide functional group is increasingly relevant in both medicinal and bioorganic chemistry. We report here practical access to a series of N2,N5-substituted five-membered cyclosulfamides. The five-membered heterocyclic motif was prepared starting
N. Aouf   +3 more
doaj   +1 more source

Imidazopyrrolone/imide copolymers Patent [PDF]

open access: yes, 1970
Synthesis and chemical properties of imidazopyrrolone/imide ...
Bell, V. L., Jr., Pezdirtz, G. F.
core   +1 more source

5,6-Dihydro-2H-pyran-3(4H)-on als Baustein zur Synthese pyrananellierter Heterocyclen [PDF]

open access: yes, 1984
Während 5,6-Dihydro-2H-pyran-3(4H)-on (3) sich mit ortho-substituierten Phenylcarbonylverbindungen nur in Einzelfällen regioselektiv zu pyrananellierten Heterocyclen umsetzt - z. B.
Eiden, Fritz, Wanner, Klaus Th.
core   +1 more source

Formation of heterocyclic aromatic amines in model systems of sucrose, lactose, amino acids and creatine [PDF]

open access: yesBIO Web of Conferences
The article presents experimental data on the study of heterocyclic aromatic amines formation in model matrices consisting of amino acids (8 essential, glutamic acid and aspartic acid), carbohydrates (sucrose, lactose) and creatine.
Utyanov Dmitry   +3 more
doaj   +1 more source

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