Unique synthesis of isochromenoindolone via reductive-oxidative cyclisation approach (Record no. 16145)
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| fixed length control field | a |
| 003 - CONTROL NUMBER IDENTIFIER | |
| control field | OSt |
| 005 - DATE AND TIME OF LATEST TRANSACTION | |
| control field | 20220201155113.0 |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
| fixed length control field | 220201b xxu||||| |||| 00| 0 eng d |
| 040 ## - CATALOGING SOURCE | |
| Original cataloging agency | AIKTC-KRRC |
| Transcribing agency | AIKTC-KRRC |
| 100 ## - MAIN ENTRY--PERSONAL NAME | |
| 9 (RLIN) | 15733 |
| Author | Kadam, Hari K. |
| 245 ## - TITLE STATEMENT | |
| Title | Unique synthesis of isochromenoindolone via reductive-oxidative cyclisation approach |
| 250 ## - EDITION STATEMENT | |
| Volume, Issue number | Vol.58(B), Jan. |
| 260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
| Place of publication, distribution, etc. | New Delhi |
| Name of publisher, distributor, etc. | CSIR |
| Year | 2021 |
| 300 ## - PHYSICAL DESCRIPTION | |
| Pagination | 104-108p. |
| 520 ## - SUMMARY, ETC. | |
| Summary, etc. | Fused heterocyclic compounds are extensively studied in medicinal chemistry due to their promising biological properties such as anticancer, antiviral, antimicrobial activities, etc.1-4 Such compounds also find a resemblance to the constituent structures of important natural products5-9 (Figure 1). Indole and isochromane based heterocyclic structures are found in several medicinally important compounds hence a fused convergent structural motif promises interesting biological properties10-13. Isochromenoindolone is one such compound with probable lead to a new class of bioactive compounds14−17. Anticipating a vast potential for medicinal studies for this compound, we directed our efforts towards developing a simple, efficient and versatile method for synthesis of isochromeno[4,3- b]indol-5(11H)-one. |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| 9 (RLIN) | 5009 |
| Topical term or geographic name entry element | GENERAL CHEMISTRY |
| 700 ## - ADDED ENTRY--PERSONAL NAME | |
| 9 (RLIN) | 15734 |
| Co-Author | Tilve, Santosh G. |
| 773 0# - HOST ITEM ENTRY | |
| Place, publisher, and date of publication | New Delhi NISCAIR-CSIR 2005 |
| Title | Indian journal of chemistry (Section B) |
| 856 ## - ELECTRONIC LOCATION AND ACCESS | |
| URL | http://nopr.niscair.res.in/bitstream/123456789/45703/1/IJCB%2058B%281%29%20104-108.pdf |
| Link text | Click here |
| 942 ## - ADDED ENTRY ELEMENTS (KOHA) | |
| Source of classification or shelving scheme | |
| Koha item type | Articles Abstract Database |
| Withdrawn status | Lost status | Source of classification or shelving scheme | Damaged status | Not for loan | Permanent Location | Current Location | Shelving location | Date acquired | Barcode | Date last seen | Price effective from | Koha item type |
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| School of Pharmacy | School of Pharmacy | Archieval Section | 2022-02-01 | 2022-0291 | 2022-02-01 | 2022-02-01 | Articles Abstract Database |