Synthesis and biological evaluation of some New fused heterocyclic azine derivatives / (Record no. 60344)

MARC details
000 -LEADER
fixed length control field 03032cam a2200337 a 4500
003 - CONTROL NUMBER IDENTIFIER
control field EG-GiCUC
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250223031705.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 170321s2016 ua 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.2016.Ma.S
100 0# - MAIN ENTRY--PERSONAL NAME
Personal name Mahmoud Aly Mourad Metwally
245 10 - TITLE STATEMENT
Title Synthesis and biological evaluation of some New fused heterocyclic azine derivatives /
Statement of responsibility, etc. Mahmoud Aly Mourad Metwally ; Supervised Magda Ahmed Abdallah , Sobhy Mohamed Gomaa
246 15 - VARYING FORM OF TITLE
Title proper/short title تشييد و تقييم النشاط البيولوجى لبعض مشتقات الازين الملتحمة متجاًسة الحلقة الجديدة
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Cairo :
Name of publisher, distributor, etc. Mahmoud Aly Mourad Metwally ,
Date of publication, distribution, etc. 2016
300 ## - PHYSICAL DESCRIPTION
Extent 172 P. ;
Dimensions 25cm
502 ## - DISSERTATION NOTE
Dissertation note Thesis (M.Sc.) - Cairo University - Faculty of Science - Department of Organic Chemistry
520 ## - SUMMARY, ETC.
Summary, etc. A new series of pyrido[2',3':4,5] pyrimido [2,1-b][1,3,5] thiadiazinones were prepared by aminomethylation of pyridopyrimidinethione with a variety of primary aromatic amines and formaldehyde solution (37%) through mannich reaction. Also, another series of pyrido[2', 3:4,5] pyrimido [2,1-b] [1,3] thiazinones were synthesized by michael addition reaction of pyridopyrimidinethione to the activated double bond of a number of arylidene malononitrile and ethyl 3-aryl-2-cyanopropenoate. The mechanism of formation of the synthesized compounds was discussed and the assigned structure was established via microanalysis and spectral data (IR, 1HNMR and Mass). In addition, the antitumor activities of the synthesized compounds were investigated and the results revealed that these compounds exhibited promising activities against HepG-2 and MCF-7 cancer cell lines. In the second project: 2-Hydrazinyl-5,7-di-p-tolylpyrido [2,3-d] pyrimidin-4 (3H)-one was prepared and condensed with different aldehydes to give the corresponding hydrazone derivatives. Oxidative cyclization of the latter compounds gave the corresponding pyrido [2,3- d] [1,2,4] triazolo [4,3-a] pyrimidin-5 (1H)-one derivatives. Furthermore, the hydrazinyl compound reacted with benzoyl chloride, triethyl orthoformate, acetyl chloride, ethyl chloroformate and carbon disulphide in alcoholic KOH solution to afford the corresponding pyrido [2,3- d][1,2,4] triazolo [4,3-a]pyrimidinones. The reaction of 2-thioxo-5,7-di-p-tolyl-2,3- dihydropyrido [2,3-d]pyrimidin-4(1H)-one or its 2-methylthio derivative with hydrazonoyl halides in dioxane under reflux, in the presence of triethylamine, yielded the corresponding pyrido 2,3-d 1,2,4triazolo 4,3-a pyrimidinones
530 ## - ADDITIONAL PHYSICAL FORM AVAILABLE NOTE
Additional physical form available note Issued also as CD
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term Azine derivatives
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term Biological evaluation
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term New fused heterocyclic
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Magda Ahmed Abdallah ,
Relator term
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Sobhy Mohamed Gomaa ,
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 Samia
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.2016.Ma.S 01010110071339000 22.09.2023 Thesis  
Dewey Decimal Classification   المكتبة المركزبة الجديدة - جامعة القاهرة مخـــزن الرســائل الجـــامعية - البدروم 11.02.2024 Cai01.12.10.M.Sc.2016.Ma.S 01020110071339000 22.09.2023 CD - Rom 71339.CD
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