Building Blocks for Artificial Anion Receptors: Derivatives of Chiral Bicyclic Guanidines

1995 ◽  
Vol 60 (4) ◽  
pp. 1039-1043 ◽  
Author(s):  
Wolfgang Peschke ◽  
Petra Schiessl ◽  
Franz P. Schmidtchen ◽  
Peter Bissinger ◽  
Annette Schier
Keyword(s):  
Building Blocks ◽  
Anion Receptors ◽  
Derivatives Of

The Coarse Scale Velocity

2017 ◽  
Author(s):  
Philip Isett
Keyword(s):  
Velocity Field ◽  
Building Blocks ◽  
Coarse Scale ◽  
Divergence Equation ◽  
Higher Derivatives ◽  
Order Of Magnitude ◽  
Derivatives Of

This chapter deals with the coarse scale velocity. It begins the proof of Lemma (10.1) by choosing a double mollification for the velocity field. Here ∈ᵥ is taken to be as large as possible so that higher derivatives of velement are less costly, and each vsubscript Element has frequency smaller than λ‎ so elementv⁻¹ must be smaller than λ‎ in order of magnitude. Each derivative of vsubscript Element up to order L costs a factor of Ξ‎. The chapter proceeds by describing the basic building blocks of the construction, the choice of elementv and the parametrix expansion for the divergence equation.

Synthesis and Biological Potentials of Quinoline Analogues: A Review of Literature

2019 ◽  
Vol 16 (7) ◽  
pp. 653-688 ◽  
Author(s):  
Leena Kumari ◽  
Salahuddin ◽  
Avijit Mazumder ◽  
Daman Pandey ◽  
Mohammad Shahar Yar ◽  
...  
Keyword(s):  
Biological Activity ◽  
Heterocyclic Compounds ◽  
Building Blocks ◽  
Vital Role ◽  
Review Of Literature ◽  
Drug Discovery Process ◽  
Active Compounds ◽  
Lead Compounds ◽  
Synthetic Approaches ◽  
Derivatives Of

Heterocyclic compounds are well known for their different biological activity. The heterocyclic analogs are the building blocks for synthesis of the pharmaceutical active compounds in the organic chemistry. These derivatives show various type of biological activity like anticancer, antiinflammatory, anti-microbial, anti-convulsant, anti-malarial, anti-hypertensive, etc. From the last decade research showed that the quinoline analogs plays a vital role in the development of newer medicinal active compounds for treating various type of disease. Quinoline reported for their antiviral, anticancer, anti-microbial and anti-inflammatory activity. This review will summarize the various synthetic approaches for synthesis of quinoline derivatives and to check their biological activity. Derivatives of quinoline moiety plays very important role in the development of various types of newer drugs and it can be used as lead compounds for future investigation in the field of drug discovery process.

scholarly journals Core-Substituted Naphthalene-diimides (cNDI) and Related Derivatives: Versatile Scaffold for Supramolecular Assembly and Functional Materials

2021 ◽  
Author(s):  
Anurag Mukherjee ◽  
Suhrit Ghosh
Keyword(s):  
Photophysical Properties ◽  
Supramolecular Assembly ◽  
Functional Materials ◽  
Building Blocks ◽  
Short Review ◽  
Molecular Engineering ◽  
Organic Optoelectronics ◽  
Naphthalene Diimide ◽  
Naphthalene Diimides ◽  
Derivatives Of

Naphthalene-diimide (NDI) derived building blocks have been explored extensively for supramolecular assembly as they exhibit attractive photophysical properties, suitable for applications in organic optoelectronics. Core-substituted derivatives of the NDI chromophore (cNDI) differ significantly from the parent NDI dye in terms of optical and redox properties. Adequate molecular engineering opportunities and substitution-dependent tunable optoelectronic properties make cNDI derivatives highly promising candidates for supramolecular assembly and functional material. This short review discusses recent development in the area of functional supramolecular assemblies based on cNDIs and related molecules.

Coupling of Steroid O-(Carboxymethyl)oxime Derivatives with Amino Alcohols

1996 ◽  
Vol 61 (2) ◽  
pp. 288-297 ◽  
Author(s):  
Vladimír Pouzar ◽  
Ivan Černý
Keyword(s):  
Amino Acids ◽  
Hydroxy Group ◽  
Building Blocks ◽  
Amino Alcohols ◽  
New Approach ◽  
Alternative Synthesis ◽  
Oxime Derivatives ◽  
A Chain ◽  
Derivatives Of

New approach to the preparation of steroids with connecting bridge, based on an O-carboxymethyloxime (CMO) structure, and with terminal hydroxy group, is presented. 17-CMO derivatives of 3β-acetoxy- and 3β-methoxymethoxyandrost-5-en-17-one were condensed with α,ω-amino alcohols to give derivatives with a chain of seven to nine atoms. After THP-protection, these compounds were converted to 3-keto-4-ene derivatives. An alternative synthesis consisted in transformation of 17-CMO derivatives with bonded amino acids by reduction of the terminal carboxyl. The resulting compounds were designed as building blocks for the preparation of bis-haptens for sandwich immunoassays.

Chiral Building Blocks for the Synthesis of Triquinane Sesquiterpenes: Derivatives of 2-Methylbicyclo[3.3.0]octan-3-ol from Catalpol

1989 ◽  
Vol 28 (4) ◽  
pp. 447-448 ◽  
Author(s):  
Klaus Weinges ◽  
Helene Iatridou ◽  
Hans-Georg Stammler ◽  
Johannes Weiss
Keyword(s):  
Building Blocks ◽  
Derivatives Of

Per-O-benzoyl-1,2-O-benzylidene derivatives of Pyranoses and Furanoses—Versatile Building Blocks for Oligosaccharide Synthesis

2017 ◽  
pp. 141-150
Author(s):  
Polina I. Abronina ◽  
Alexander I. Zinin ◽  
Nikita M. Podvalnyy ◽  
Leonid O. Kononov ◽  
Sandip Pasari
Keyword(s):  
Building Blocks ◽  
Oligosaccharide Synthesis ◽  
Derivatives Of

scholarly journals Rearrangement of spiroderivatives of 1,3-benzo(naphtho)dioxin-4(1)-ones as a new method of synthesis of xanthene bromo derivatives

2021 ◽  
pp. 73-77
Author(s):  
A.V. Kovtun ◽  
◽  
S.A. Varenichenko ◽  
E.V. Zaliznaya ◽  
A.V. Mazepa ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
13C Nmr ◽  
Bromine Atom ◽  
Sodium Perchlorate ◽  
Building Blocks ◽  
Dimethylamino Group ◽  
1H And 13C Nmr ◽  
Molecular Building Blocks ◽  
Derivatives Of ◽  
Fold Excess

We have proposed a method for the synthesis of previously unknown bromo xanthenes using the reagent PBr3/DMF as a rearrangement initiator. Bromo derivatives of xanthenes in the form of organic perchlorates were prepared by reacting the corresponding benzo(naphtho)dioxin-4(1)-ones with a three-fold excess of Vilsmeier-Haack PBr3/DMF reagent at 1100C for 2 hours, followed by the addition of sodium perchlorate. The conditions for the synthesis of formyl derivatives of xanthenes under conditions of acid hydrolysis were selected. The structure of the compounds was confirmed by 1H and 13C NMR spectral data and mass spectrometry. Preliminary studies showed that it is possible to selectively replace the dimethylamino group and the bromine atom with various nucleophiles in bromo derivatives of xanthenes, which opens up wide possibilities for the synthesis of low-molecular building blocks and dyes.

2-Azaanthraquinones: Building Blocks for New Ring-Fused Imidazoles and their Transformation into Benzo[f]isoindole-4,9-diones

2005 ◽  
Vol 60 (7) ◽  
pp. 771-779 ◽  
Author(s):  
Birgit Frank ◽  
Rainer Beckert ◽  
Sven Rau ◽  
Helmar Görls
Keyword(s):  
Building Blocks ◽  
Substituted Acetylenes ◽  
Derivatives Of

The modification of 2-azaanthraquinones with selected C1 building blocks gives a series of new imidazo-fused derivatives. Employing 2,3-dichloro-5,6-dicyanopyrazine as cyclization partner a rearrangement to yield derivatives of benzo[f ]isoindole-4,9-dione takes place. The Sonogashira crosscoupling reaction of the aminalester derivative of the azaanthraquinone resulted in well soluble silyl substituted acetylenes as well as ethinyl aniline which allows further derivatization reactions.

Synthesis of Sterically Congested Carbamates of Carbohydrates through Organic Base Catalysis

Synthesis ◽  
2019 ◽  
Vol 51 (15) ◽  
pp. 2897-2908 ◽  
Author(s):  
Anji Chen ◽  
Dan Wang ◽  
Lalith P. Samankumara ◽  
Guijun Wang
Keyword(s):  
Hydroxy Group ◽  
Current Method ◽  
Building Blocks ◽  
Base Catalysis ◽  
Organic Base ◽  
Molecular Assemblies ◽  
Effective Catalyst ◽  
Organic Bases ◽  
Derivatives Of ◽  
General Method

4,6-O-Benzylidene acetal protected α-methoxy d-glucose and d-glucosamine are useful building blocks for the syntheses of carbohydrate derivatives and functional molecular assemblies. In this research, we have developed a general method for the preparation of C-3 carbamate derivatives of densely functionalized glucose and glucosamine with isocyanates using organic bases as catalysts. Without a suitable catalyst, the C-3 hydroxy group of the glucosamine derivative could not be converted into the corresponding carbamates when treated with isocyanates. Several organic bases were screened as the catalysts for the reactions, and we discovered that 5.0 mol% of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) was an effective catalyst for the carbamoylation reaction. A library of both alkyl and aryl carbamate derivatives of the two sterically congested carbohydrates have been effectively synthesized using the current method.

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