Cucurbiturils Monofunctionalized on the Methylene Bridge and their Host‐Guest Properties

Author(s):  
Marketa Kandrnalova ◽  
Vladimir Sindelar
Keyword(s):  
Planta Medica ◽  
2012 ◽  
Vol 78 (05) ◽  
Author(s):  
F Zulfiqar ◽  
S Ross ◽  
D Slade ◽  
S Ahmed ◽  
MM Radwan ◽  
...  

2009 ◽  
Vol 6 (3) ◽  
pp. 866-870
Author(s):  
CH. Sridevi ◽  
K. Balaji ◽  
A. Naidu ◽  
R. Sudhakaran

2,3-Diphenyl quinoxaline(SI)was fused with 2-amino benzothiazoles(SII)by a methylene bridge, which was then allowed for acetylation. The acetylated product (SIV) was made to react with different aromatic aldehydes to give chalcones(SV1-SV5). Chalcones refluxed with substituted acid hydrazides to afford different phenyl pyrazolo benzothiazolo quinoxaline derivatives(SVI1-SVI15). The structure of chalcones and phenyl pyrazolo benzothiazolo quinoxaline derivatives were confirmed by M.P, TLC and spectral data. All the synthesized compounds were screened for their antimicrobial activities.


2018 ◽  
Vol 10 (3) ◽  
pp. 1380-1389 ◽  
Author(s):  
Ahmed S. Abdelkhalek ◽  
Genevieve S. Alley ◽  
Osama I. Alwassil ◽  
Shailesh Khatri ◽  
Philip D. Mosier ◽  
...  

ARKIVOC ◽  
2005 ◽  
Vol 2005 (9) ◽  
pp. 159-164 ◽  
Author(s):  
Enrique Díez-Barra ◽  
Javier Guerra ◽  
Valentín Hornillos ◽  
Sonia Merino ◽  
Julián Rodríguez-López ◽  
...  

2014 ◽  
Vol 16 (9) ◽  
pp. 2446-2449 ◽  
Author(s):  
Laura Gilberg ◽  
Muhammad S. A. Khan ◽  
Marketa Enderesova ◽  
Vladimir Sindelar
Keyword(s):  

2014 ◽  
Vol 43 (14) ◽  
pp. 5443 ◽  
Author(s):  
Anangamohan Panja ◽  
Milan Shyamal ◽  
Amrita Saha ◽  
Tarun Kanti Mandal

Synthesis ◽  
2018 ◽  
Vol 50 (06) ◽  
pp. 1246-1258
Author(s):  
Udo Nubbemeyer ◽  
Adile Duymaz ◽  
Jochen Körber ◽  
Carolin Hofmann ◽  
Dorothea Gerlach

The synthesis of lipoxin A4 and B4 analogues (LXA4, LXB4) to gain access to stabilized inflammation resolving compounds is an important field of research. Starting from known structural requirements of the natural compounds displaying biological activity and a broad investigation of their rapid metabolism, various LXA4 derivatives have been developed and tested. Focusing on variation and stabilization of the conjugated E,E,Z,E C7–C14 tetraene moiety of natural LXA4, a methylene bridge introduced between C9 and C14 might suppress any Z/E isomerization of the C11–C12 olefin. Intending to enable at least known structure variations in connection with the C1–C7 and the C15–C20 fragments, a convergent total synthesis starting from a known cycloheptatriene is developed. The C1–C8 building blocks are generated via six-step ex-chiral pool sequences starting from 2-deoxy-d-ribose delivering two 5,6-dihydroxy carboxylic acid derivatives with C7 aldehyde functions. The synthesis of the C8–C21 building block starts from a known cycloheptatriene 1-carbonester (C8–C14, C21) and hexanoyl chloride (C15–C20). After Friedel–Crafts-type coupling, the defined configuration of the C15 OH group is introduced via enantioselective reduction of the ketone precursor. Following an additional four steps, an aryl sulfone C9–C21 building block is completed ready for a key Julia–Kocienski olefination with the C1–C7 compounds. Finally, removal of the protecting groups completes the synthesis of the target optically active 9,14-methylene LXA4 methyl ester.


1985 ◽  
Vol 63 (3) ◽  
pp. 632-635 ◽  
Author(s):  
V. K. Mahesh ◽  
Mamta Maheswari ◽  
Rakesh Sharma ◽  
Rashmi Sharma

Tetrahydrocannabinol 1, the active constituent of CannabissativaLinn, is a well-known CNS-active compound and introduction of a nitrogen atom at the ring junction of the pyran and alicyclic ring is of considerable interest. This prompted the synthesis of 7H-indolo[1,2-c] [1,3]-, 5H-imidazolo[1,2-C] [1,3],- and 7H-benzimidazolo[1,2-c] [1,3]-benzoxazine, a novel heterocyclic system. 2-(2′-Hydroxyphenyl) indoles, 2-(2′-hydroxyphenyl) imidazoles, and 2-(2′-hydroxyphenyl) benzimidazoles are suitable intermediates for the preparation of this type of benzoxazines, as the second heterocycle (ring B) can then be constructed by introduction of a methylene bridge between the hydroxyl of the 2′-hydroxy phenyl substituent and the imino group of the heterocyclic system.


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