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Synthesis and biological evaluation of some new fused heterocyclic azine derivatives as antimicrobial agents / (Record no. 63980)

MARC details
000 -LEADER
fixed length control field 03099cam a2200325 a 4500
003 - CONTROL NUMBER IDENTIFIER
control field EG-GiCUC
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250223031855.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 171212s2017 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.2017.Am.S
100 0# - MAIN ENTRY--PERSONAL NAME
Personal name Amany Mohamed Gad Mohamed
245 10 - TITLE STATEMENT
Title Synthesis and biological evaluation of some new fused heterocyclic azine derivatives as antimicrobial agents /
Statement of responsibility, etc. Amany Mohamed Gad Mohamed ; Supervised Sobhy Mohamed Gomha
246 15 - VARYING FORM OF TITLE
Title proper/short title تشييد و تقييم النشاط البيولوجى لبعض مشتقاث الأزين الملتحمة غير متجانسة الحلقة الجديدة كمضاد للميكروبات
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Cairo :
Name of publisher, distributor, etc. Amany Mohamed Gad Mohamed ,
Date of publication, distribution, etc. 2017
300 ## - PHYSICAL DESCRIPTION
Extent 170 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. In the first project: 1,3-Di(thiophen-2-yl)prop-2-en-1-one was utilized for the synthesis of 4,6- di(thiophen-2-yl)-3,4-dihydropyrimidine-2(1H)-thione and 5,7-di(thiophen-2-yl)-2-thioxo-2,3- dihydropyrido[2,3-d]pyrimidin-4(1H)-one. The latter thiones were used for the synthesis of two new series of [1,2,4]triazolo[4,3-a]pyrimidines and pyrido[2,3-d][1,2,4]triazolo[4,3-a]pyrimidinones via reaction with the appropriate hydrazonoyl halides using triethylamine as a basic catalyst. The mechanism of formation of the synthesized compounds was discussed and the assigned structure was established via microanalysis, spectral data (IR, 1HNMR and mass) and quantum chemistry calculations. Moreover, the newly synthesized products were evaluated for their antimicrobial activities and the results show that some derivatives have good to mild activities. Moreover, quantum chemistry calculations studies are confirming the structure of the products. In the second project: Starting with different primary aromatic amines and formaldehyde solution (37%), a series of pyrido[2',3':4,5]pyrimido[2,1-b][1,3,5]thiadiazinones was synthesized by aminomethylation of pyridopyrimidinethione via Mannich reaction in acidic conditions. Moreover, another series of pyrido[2',3:4,5]pyrimido[2,1-b][1,3]thiazinones was prepared by Micheal addition reaction of pyridopyrimidinethione to the activated double bond of a number of arylidene malononitrile and 2-(benzo[d][1,3]dioxol-5-ylmethylene)malononitrile. In addition, treatment of 2-hydrazinyl-5,7-di(thiophen-2-yl)pyrido[2,3-d]pyrimidin-4(3H)-one with the proper aldehydes, and terephthaldehyde in refluxing acetic acid in and a few drops of hydrochloric acid afforded the corresponding hydrazones derivatives, and bis-hydrazone(s), respectively
530 ## - ADDITIONAL PHYSICAL FORM AVAILABLE NOTE
Additional physical form available note Issued also as CD
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term Antimicrobial agents
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term Fused heterocyclic azine derivatives
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term Synthesis and biological evaluation
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Sobhy Mohamed Gomha ,
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.2017.Am.S 01010110073708000 22.09.2023 Thesis  
Dewey Decimal Classification   المكتبة المركزبة الجديدة - جامعة القاهرة مخـــزن الرســائل الجـــامعية - البدروم 11.02.2024 Cai01.12.10.M.Sc.2017.Am.S 01020110073708000 22.09.2023 CD - Rom 73708.CD