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Synthesis of some new azines and their fused derivatives of expected biological activity / (Record no. 67496)

MARC details
000 -LEADER
fixed length control field 02758cam a2200349 a 4500
003 - CONTROL NUMBER IDENTIFIER
control field EG-GiCUC
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250223032044.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 180917s2017 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.2017.Kh.S
100 0# - MAIN ENTRY--PERSONAL NAME
Personal name Khalid Gamal Salah Eldin Mohamed
245 10 - TITLE STATEMENT
Title Synthesis of some new azines and their fused derivatives of expected biological activity /
Statement of responsibility, etc. Khalid Gamal Salah Eldin Mohamed ; Supervised Nadia Hanafy Metwally , Mohamed Mohamed Mohamed Youssef , Rasha Abdelaziz Mohamed Faty
246 15 - VARYING FORM OF TITLE
Title proper/short title تشييد بعض الأزينات الجديدة ومشتقاتها الملتحمة ذات نشاط بيولوجي متوقع
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Cairo :
Name of publisher, distributor, etc. Khalid Gamal Salah Eldin Mohamed ,
Date of publication, distribution, etc. 2017
300 ## - PHYSICAL DESCRIPTION
Extent 124 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. The condensation of 2-cyano-N-(6-methylpyridin-2-yl)acetamide (3) with various aromatic aldehydes afforded the corresponding arylidenes. On the other hand, compound 3 was treated with pentane-2,4-dione gave the corresponding 2-pyridinone derivative 10. Also, cyclocondensation of compound 3 with salicylaldehyde derivatives afforded 2-iminochromene derivatives 12a,b. Coupling of compounds 3 with aryldiazonium chlorides led to the formation of 2-arylhydrazono derivatives 15a-f. The reaction of compounds 3 with phenyl isothiocyanate, followed by addition of Ü-haloesters afforded thiazole derivatives. The 5-amino pyrazole derivative 21 reacted with some active methylene compounds such as acetyl acetone and ethyl acetoacetate to give pyrazolopyrimidines. Treatment of enaminone derivative 26 with hydrazine hydrate or phenylhydrazine yielded aminopyrazoles 28a,b, respectively. Refluxing of enaminone 26 with diaminopyrazoles afforded compounds 30a-e. Also, reaction of enaminone derivative with guindine nitrate afforded diaminopyrimidine derivative 32. The structure of all the newly synthesized compounds was elucidated by elemental analyses, spectral data and plausible mechanisms have been postulated to account for their formation.The anticancer activity of some new selected products was also investigated
530 ## - ADDITIONAL PHYSICAL FORM AVAILABLE NOTE
Additional physical form available note Issued also as CD
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term 2-Cyano-N-(6-methylpyridin-2-yl)acetamide
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term 2-Imino-chromenes
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term Pyridines
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Mohamed Mohamed Mohamed Youssef ,
Relator term
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Nadia Hanafy Metwally ,
Relator term
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Rasha Abdelaziz Mohamed Faty ,
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.2017.Kh.S 01010110075755000 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.Kh.S 01020110075755000 22.09.2023 CD - Rom 75755.CD