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New routes for synthesis of biologically interestingpolyfunctional heteroaromatics utilizing an enamine precursor / (Record no. 48444)

MARC details
000 -LEADER
fixed length control field 019770000a22003490004500
003 - CONTROL NUMBER IDENTIFIER
control field EG-GICUC
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250223031112.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 060917s2006 ua a 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.2006.Am.U.
100 0# - MAIN ENTRY--PERSONAL NAME
Personal name Amr Salah AbouZeid
245 10 - TITLE STATEMENT
Title New routes for synthesis of biologically interestingpolyfunctional heteroaromatics utilizing an enamine precursor /
Statement of responsibility, etc. Amr Salah AbouZeid ; Supervised Mohamed Helmy Elnagdi , Fatma Mohamed Manhi
246 15 - VARYING FORM OF TITLE
Title proper/short title طرق جديدة لتخليق ا لحلقيات غير المتجانسة عديدة المجموعة الدالة وذات النشاط البيولوجى المتوقع باستخدام الاينامينات كمواد اولية
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Cairo :
Name of publisher, distributor, etc. Amr Salah AbouZeid ,
Date of publication, distribution, etc. 2006
300 ## - PHYSICAL DESCRIPTION
Extent 157P :
Other physical details ill ;
Dimensions 30cm
502 ## - DISSERTATION NOTE
Dissertation note Thesis (M.Sc.) - Cairo University - Faculty Of Science - Department Of Organic Chemistry
520 ## - SUMMARY, ETC.
Summary, etc. 2 - Acetylnaphthalene 1 condenses with dimethylformamide dimethylacetal (DMFDMA) yielding enaminone 2 , best yield was obtained by heating in a domestic microwave oven at full power for 5 minutes (85in hundred) The formed E enaminone 2 reacted with 2amino4methylthiazole 3 , 4aminopyridine 4 and Osubstituted aniline 5ac yielding the Z enaminones , predomination of Z form due to the fixation of this form by hydrogen bond (cfFigure 1) ; Although 2aminobenzothiazole 9 afforded a mixture of E enaminone 10 and Z - enaminone 11in ratio 4 : 6 as indicated from 1H NMR (cfFigure 2)
530 ## - ADDITIONAL PHYSICAL FORM AVAILABLE NOTE
Additional physical form available note Issued also as CD
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term Enaminones
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term pyrazoles
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term pyrimidines
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term quinolinone
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Fatma Mohamed Manhi ,
Relator term
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Mohamed Hilmy Elnagdi ,
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 Amira
Reviser Cataloger
905 ## - LOCAL DATA ELEMENT E, LDE (RLIN)
Cataloger Mustafa
Reviser Revisor
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
Dewey Decimal Classification   المكتبة المركزبة الجديدة - جامعة القاهرة قاعة الرسائل الجامعية - الدور الاول 11.02.2024 Cai01.12.10.M.Sc.2006.Am.U. 01010110045280000 22.09.2023 Thesis
Dewey Decimal Classification   المكتبة المركزبة الجديدة - جامعة القاهرة مخـــزن الرســائل الجـــامعية - البدروم 11.02.2024 Cai01.12.10.M.Sc.2006.Am.U. 01020110045280000 22.09.2023 CD - Rom