Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Shunichi Fukuzumi | * |
dc.date.accessioned | 2016-08-28T12:08:32Z | - |
dc.date.available | 2016-08-28T12:08:32Z | - |
dc.date.issued | 2011 | * |
dc.identifier.issn | 1523-7060 | * |
dc.identifier.other | OAK-7489 | * |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/221553 | - |
dc.description.abstract | Both bacteriopyropheophorbide-a and ring-B reduced pyropheophorbide-a on reacting with NBS (N-bromosuccinamide) undergo electrophilic bromination to provide 10-bromo analogs. The electronic nature of the substituents present at position-3 did not make any difference in the regioselective outcome of the brominated products. These relatively stable brominated chlorins and bacteriochlorins provide an easy way of introducing a wide variety of functionalities, which could be extremely useful in developing improved agents for biomedical applications and supramolecular chemistry. © 2011 American Chemical Society. | * |
dc.language | English | * |
dc.title | Remarkable regioselective position-10 bromination of bacteriopyropheophorbide-a and ring-b reduced pyropheophorbide-a | * |
dc.type | Article | * |
dc.relation.issue | 8 | * |
dc.relation.volume | 13 | * |
dc.relation.index | SCI | * |
dc.relation.index | SCIE | * |
dc.relation.index | SCOPUS | * |
dc.relation.startpage | 1956 | * |
dc.relation.lastpage | 1959 | * |
dc.relation.journaltitle | Organic Letters | * |
dc.identifier.doi | 10.1021/ol200314v | * |
dc.identifier.wosid | WOS:000289187200016 | * |
dc.identifier.scopusid | 2-s2.0-79955452471 | * |
dc.author.google | Ethirajan M. | * |
dc.author.google | Joshi P. | * |
dc.author.google | William W.H. | * |
dc.author.google | Ohkubo K. | * |
dc.author.google | Fukuzumi S. | * |
dc.author.google | Pandey R.K. | * |
dc.contributor.scopusid | Shunichi Fukuzumi(35430038100;58409757400) | * |
dc.date.modifydate | 20240401081001 | * |