New approaches for the synthesis of novel heterocyclic compounds derived from cyanomethylene and Ý-diketone compounds and determination of their biological effect / (Record no. 76814)

MARC details
000 -LEADER
fixed length control field 02894cam a2200337 a 4500
003 - CONTROL NUMBER IDENTIFIER
control field EG-GiCUC
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250223032529.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 200229s2020 ua d f m 000 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency EG-GiCUC
Language of cataloging eng
Transcribing agency EG-GiCUC
041 0# - LANGUAGE CODE
Language code of text/sound track or separate title eng
049 ## - LOCAL HOLDINGS (OCLC)
Holding library Deposite
097 ## - Thesis Degree
Thesis Level M.Sc
099 ## - LOCAL FREE-TEXT CALL NUMBER (OCLC)
Classification number Cai01.12.10.M.Sc.2020.Ib.N
100 0# - MAIN ENTRY--PERSONAL NAME
Personal name Ibram Refat Boshra Mikhail
245 10 - TITLE STATEMENT
Title New approaches for the synthesis of novel heterocyclic compounds derived from cyanomethylene and Ý-diketone compounds and determination of their biological effect /
Statement of responsibility, etc. Ibram Refat Boshra Mikhail ; Supervied Rafat Milad Mohareb , Noha M. H. Elnagdi
246 15 - VARYING FORM OF TITLE
Title proper/short title إتجاهات جديدة لتحضير مركبات جديدة غير متجانسة الحلقة مشتقة من مركبات السيانوميثيلين والبيتا ثنائى الكيتون وتعيين تأثيرها البيولوجى
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Cairo :
Name of publisher, distributor, etc. Ibram Refat Boshra Mikhail ,
Date of publication, distribution, etc. 2020
300 ## - PHYSICAL DESCRIPTION
Extent 169 P. :
Other physical details charts ;
Dimensions 25cm
502 ## - DISSERTATION NOTE
Dissertation note Thesis (M.Sc.) - Cairo University - Faculty of Science - Department of Organic Chemistry
520 ## - SUMMARY, ETC.
Summary, etc. Pyrazoles are an important heterocyclic family due to their wide spectrum of biological properties such as the anti-proliferative activities and inhibition toward tyrosine kinases. In the present work we started with pyrazole derivative (3) produced through the reaction of ethyl benzoylacetate (1) with hydrazine hydrate (2) followed by its heterocyclization to produce fused derivatives. The target compounds were synthesized in steps outlined in Schemes 1-6. The reaction of the pyrazole (3) with elemental sulfur and phenylisothiocyanate (4) gave the derivative (5). The molecular structure of compound (5) was confirmed on the basis of its elemental and spectral data. On the other hand, the reaction of compound (3) with ethyl orthoformate gave the 4-ethoxymethyleno derivative (6). The presence of the ketone and the active methylene moieties in compound (3) enhanced the synthesis of thieno[3,2-c]pyrazol derivatives using Gewald{u2019}s thiophene synthesis. Next, we moved towards the formation of some heterocyclic compounds starting from compound (3). The anti-proliferative activities of the newly synthesized compounds were evaluated against the six cancer cell lines. It is clear that compounds 8b, 9, 12b, 12d, 14b, 15b, 18d, 18f, 19b and 21d were the most active compounds. Several tests as Melting point, IR spectra, ¹H-NMR spectra, Mass spectra and analytical data (element analysis) have been made on all components
530 ## - ADDITIONAL PHYSICAL FORM AVAILABLE NOTE
Additional physical form available note Issued also as CD
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term Pyran
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term Pyrazol derivatives
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term Pyridine
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Noha M. H. Elnagdi ,
Relator term
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Rafat Milad Mohareb ,
Relator term
856 ## - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="http://172.23.153.220/th.pdf">http://172.23.153.220/th.pdf</a>
905 ## - LOCAL DATA ELEMENT E, LDE (RLIN)
Cataloger Nazla
Reviser Revisor
905 ## - LOCAL DATA ELEMENT E, LDE (RLIN)
Cataloger Shimaa
Reviser Cataloger
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Dewey Decimal Classification
Koha item type Thesis
Holdings
Source of classification or shelving scheme Not for loan Home library Current library Date acquired Full call number Barcode Date last seen Koha item type Copy number
Dewey Decimal Classification   المكتبة المركزبة الجديدة - جامعة القاهرة قاعة الرسائل الجامعية - الدور الاول 11.02.2024 Cai01.12.10.M.Sc.2020.Ib.N 01010110080903000 22.09.2023 Thesis  
Dewey Decimal Classification   المكتبة المركزبة الجديدة - جامعة القاهرة مخـــزن الرســائل الجـــامعية - البدروم 11.02.2024 Cai01.12.10.M.Sc.2020.Ib.N 01020110080903000 22.09.2023 CD - Rom 80903.CD
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