Part 1 _ Ortho_hydroxy_w_halo_acetophenones as starting materials in the rasoda reactions for the synthesis of flavonols Part 2 _ Synthesis of 2_aroyl_coumaranones and the corresponding flavonols from ortho_hydroxy_w_mono_and_di_halo_acetophenones Part 3 _ Synthesis of 2_4_dimethyl_8_acetyl_7_6_furo_coumarin and the corresponding furo_coumarone Part 4 _ Determination of the structure of some of the products derived from ortho_hydroxy and acetoxy_chalkone dibromides

Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/154335

Full metadata record

DC Field	Value	Language
dc.coverage.spatial	Chemistry
dc.date.accessioned	2017-06-13T08:57:14Z	-
dc.date.available	2017-06-13T08:57:14Z	-
dc.identifier.uri	http://hdl.handle.net/10603/154335	-
dc.description.abstract	Abstract not available newline newline
dc.format.extent	iii, 286p.
dc.language	English
dc.relation	-
dc.rights	university
dc.title	Part 1 _ Ortho_hydroxy_w_halo_acetophenones as starting materials in the rasoda reactions for the synthesis of flavonols Part 2 _ Synthesis of 2_aroyl_coumaranones and the corresponding flavonols from ortho_hydroxy_w_mono_and_di_halo_acetophenones Part 3 _ Synthesis of 2_4_dimethyl_8_acetyl_7_6_furo_coumarin and the corresponding furo_coumarone Part 4 _ Determination of the structure of some of the products derived from ortho_hydroxy and acetoxy_chalkone dibromides
dc.title.alternative	-
dc.creator.researcher	Pendse, Hrishikesh Krishna
dc.subject.keyword	Ortho-hydroxy
dc.subject.keyword	Acetoxy
dc.subject.keyword	Dimethyl
dc.subject.keyword	Furo-coumarone
dc.subject.keyword	Dibromides
dc.description.note	-
dc.contributor.guide	Limaye, S D
dc.publisher.place	Pune
dc.publisher.university	Savitribai Phule Pune University
dc.publisher.institution	Department of Chemistry
dc.date.registered	n.d.
dc.date.completed	1954
dc.date.awarded	n.d.
dc.format.dimensions	-
dc.format.accompanyingmaterial	None
dc.source.university	University
dc.type.degree	Ph.D.
Appears in Departments:	Department of Chemistry

Files in This Item:

File	Description	Size	Format
/01_title.pdf	Attached File	81.33 kB	Adobe PDF	View/Open
01_title.pdf		81.33 kB	Adobe PDF	View/Open
02_acknowledgements.pdf		70.48 kB	Adobe PDF	View/Open
03_preface.pdf		192.73 kB	Adobe PDF	View/Open
04_contents.pdf		81.01 kB	Adobe PDF	View/Open
05_part i.pdf		5.58 MB	Adobe PDF	View/Open
06_part ii.pdf		4.1 MB	Adobe PDF	View/Open
07_part iii.pdf		1.28 MB	Adobe PDF	View/Open
08_part iv.pdf		3.09 MB	Adobe PDF	View/Open
09_list of new compounds.pdf		552.11 kB	Adobe PDF	View/Open

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