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Synthesis of some fused heterocyclic compounds incorporating isoquinoline moiety with expected biological activity / (Record no. 79265)

MARC details
000 -LEADER
fixed length control field 03060cam a2200349 a 4500
003 - CONTROL NUMBER IDENTIFIER
control field EG-GiCUC
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250223032645.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 201219s2020 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.2020.Ya.S
100 0# - MAIN ENTRY--PERSONAL NAME
Personal name Yara Nour Eldin Mohamed Laboud
245 10 - TITLE STATEMENT
Title Synthesis of some fused heterocyclic compounds incorporating isoquinoline moiety with expected biological activity /
Statement of responsibility, etc. Yara Nour Eldin Mohamed Laboud ; Supervised Hyam A. Abdelhadi , Mohamed A. Mohamed Teleb , Fatma M. Saleh
246 15 - VARYING FORM OF TITLE
Title proper/short title تحضير بعض المركبات الملتحمة غير متجانسة الحلقة متضمنة جزئية الأيزوكينولين و المتوقع لها نشاط بيولوجى
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Cairo :
Name of publisher, distributor, etc. Yara Nour Eldin Mohamed Laboud ,
Date of publication, distribution, etc. 2020
300 ## - PHYSICAL DESCRIPTION
Extent 98 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. The present dissertation describes the utility of isoquinoline derivatives in the synthesis of new heterocyclic compounds by treatment of 2-(6,7-dimethoxy-3,4-dihydroisoquinolin-1- yl)acetonitrile 1 with arylisothiocycnates 2a-c in refluxing toluene to afford thioanilide derivatives 3, which converted to the corresponding thiadiazole derivatives 5A-P upon refluxing with Ü-ketohydrazonoyl halides 4A-P in chloroform in the presence of triethylamine. Refluxing of thiadiazoles 5A-C with N,N-dimethylformamide dimethylacetal afforded enaminones 11A-C. Also, study the Michael addition reaction of enaminones 14a-d with compound 1 in refluxing ethanol in the presence of piperidine to yield 4H-pyrido[2,1-a]isoquinoline-1-carbonitrile derivatives 16a-d. Also, reaction of and ethyl 3-aryl-2-cyanoacrylate 19a-g with compound 1 under the same previous conditions, using acetonitrile instead of ethanol, gave 4H-pyrido[2,1- a]isoquinoline-1,3-dicarbonitrile derivatives 23a-g. Stirring of aldehydes 24a-i with 1 in absolute ethanol in the presence of concentrated hydrochloric acid gave the corresponding arylidene derivatives 25, which converted to 5,6-dihydropyrrolo[2,1-a]isoquinoline-1-carbonitrile derivatives 28a-g by refluxing with Ü-ketohydrazonoyl halides 4A,G,K in chloroform in the presence of triethylamine. The structures of the new heterocyclic compounds prepared were established on the basis of elemental analysis and spectral analyses (IR, ¹H NMR, ¹³C NMR, MS). Also, some of the new compounds were tested for their antibacterial and antifungal activities
530 ## - ADDITIONAL PHYSICAL FORM AVAILABLE NOTE
Additional physical form available note Issued also as CD
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term 2-(6,7-dimethoxy-3,4-dihydroisoquinolin-1-yl)acetonitrile
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term Thiadiazole
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term Ü- ketohydrazonoyl halide
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Fatma M. Saleh ,
Relator term
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Hyam A. Abdelhadi ,
Relator term
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Mohamed A. Mohamed Teleb ,
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.Ya.S 01010110082338000 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.Ya.S 01020110082338000 22.09.2023 CD - Rom 82338.CD