N-Heterocyclic carbene-catalyzed synthesis of oxazolones, e-Lactones and N-N Axially chiral molecules (Record no. 429625)

MARC details
000 -LEADER
fixed length control field 02047nam a22002417a 4500
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 230818b |||||||| |||| 00| 0 eng d
041 ## - LANGUAGE CODE
Language code of text/sound track or separate title en
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 547
Item number KUR
100 ## - MAIN ENTRY--PERSONAL NAME
Personal name Balanna, Kuruva
245 ## - TITLE STATEMENT
Title N-Heterocyclic carbene-catalyzed synthesis of oxazolones, e-Lactones and N-N Axially chiral molecules
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT)
Place of publication, distribution, etc Bangalore :
Name of publisher, distributor, etc IISc ,
Date of publication, distribution, etc 2023 .
300 ## - PHYSICAL DESCRIPTION
Extent v, 192p.
Other physical details col. ill. ;
Dimensions 29.1 cm * 20.5 cm
Accompanying material e-Thesis
Size of unit 16.38Mb
500 ## - GENERAL NOTE
General note include bibliographic reference and index
502 ## - DISSERTATION NOTE
Dissertation note PhD; 2023; Organic chemistry
520 ## - SUMMARY, ETC.
Summary, etc The diverse reactivity of N-heterocyclic carbenes (NHCs) in organocatalysis is due to the possibility of different modes of action. Although NHC-bound enolates and dienolates were well-known, the NHC-bound cross-conjugated aza-trienolates were undisclosed. We have demonstrated the synthesis of pyrrolooxazolones via NHC-bound azatrienolate intermediates. In the same fashion, involvement of chiral alpha-carbon center (proximal reaction centre) in dynamic kinetic resolution (DKR) via NHC-bound enolates were known. However, the gamma, gamma-disubstituted chiral carbon center (remote reaction centre) involving in DKR via NHC-bound dienolates were unknown. We have recently demonstrated the DKR of gamma,gamma-disubstituted indole 2-carboxaldehydes via NHC-Lewis acid cooperative catalysis for the synthesis of tetracyclic epsilon-lactones. Additionally, NHC-catalyzed atroposelective synthesis of C-C and C-N axially chiral molecules were known, and the asymmetric synthesis of axially chiral N-N molecules remains unknown in carbene catalysis. We have demonstrated the N-heterocyclic carbene (NHC)-catalyzed selective amidation reaction leading to the atroposelective synthesis of N-N axially chiral 3-amino quinazolinones.
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element N-heterocyclic carbene
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element dynamic kinetic resolution
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element N-N axially chiral molecules
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element pyrrolooxazolones
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Biju, Akkattu T advised
856 ## - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier https://etd.iisc.ac.in/handle/2005/6191
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Thesis
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Home library Current library Date acquired Total Checkouts Full call number Barcode Date last seen Koha item type
    Dewey Decimal Classification     JRD Tata Memorial Library JRD Tata Memorial Library 18/08/2023   547 KUR ET00204 18/08/2023 E-BOOKS

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