| dc.contributor.author | Guchhait, Goutam | |
| dc.contributor.author | Misra, Anup Kumar | |
| dc.date.accessioned | 2012-11-23T07:04:46Z | |
| dc.date.available | 2012-11-23T07:04:46Z | |
| dc.date.issued | 2009-08-12 | |
| dc.identifier | FOR ACCESS / DOWNLOAD PROBLEM -- PLEASE CONTACT LIBRARIAN, BOSE INSTITUTE, akc@bic.boseinst.ernet.in | en_US |
| dc.identifier.citation | Guchhait G and Misra A K (2009) Total synthesis of the heptasaccharide of the iron-binding exopolysaccharide secreted by Klebsie/a oxytoca BAS-1 0, Tetrahedron: Asymmetry 20, 1 791-1 79 7. | en_US |
| dc.identifier.issn | 0957-4166 | |
| dc.identifier.uri | 1. Full Text Link -> | en_US |
| dc.identifier.uri | http://ac.els-cdn.com/S095741660900545X/1-s2.0-S095741660900545X-main.pdf?_tid=580b7136-353b-11e2-8c88-00000aab0f02&acdnat=1353654157_cc1ee4d1d9cf4771d380d6010dc55003 | en_US |
| dc.identifier.uri | ================================================= | en_US |
| dc.identifier.uri | 2. Scopus : Citation Link -> | en_US |
| dc.identifier.uri | http://www.scopus.com/record/display.url?eid=2-s2.0-69249162204&origin=resultslist&sort=plf-f&src=s&st1=Total+synthesis+of+the+heptasaccharide+repeating+unit+of+the+iron-binding+exopolysaccharide+secreted+by+Klebsiella+oxytoca+BAS-10&sid=C3_e4E2QzwBcVp0oijnKmUS%3a400&sot=b&sdt=b&sl=149&s=TITLE-ABS-KEY-AUTH%28Total+synthesis+of+the+heptasaccharide+repeating+unit+of+the+iron-binding+exopolysaccharide+secreted+by+Klebsiella+oxytoca+BAS-10%29&relpos=0&relpos=0&searchTerm=TITLE-ABS-KEY-AUTH(Total%20synthesis%20of%20the%20heptasaccharide%20repeating%20unit%20of%20the%20iron-binding%20exopolysaccharide%20secreted%20by%20Klebsiella%20oxytoca%20BAS-10) | en_US |
| dc.description | DOI : 10.1016/j.tetasy.2009.07.009 | en_US |
| dc.description.abstract | The first total synthesis of a heptasaccharide found in the iron-binding exopolysaccharide produced by Klebsiella oxytoca BAS-10 has been achieved in excellent yield using a block synthetic strategy. A trisaccharide glycosyl donor was stereoselectively coupled with a tetrasaccharide glycosyl acceptor using the trichloroacetimidate activation procedure. The yields and stereo outcome were excellent in each step of glycosylation. A late stage oxidation protocol was adopted for the oxidation of the primary hydroxyl group to the carboxylic functionality while keeping a secondary hydroxyl group unaffected. | en_US |
| dc.description.sponsorship | CSIR, New Delhi
Ramanna Fellowship (AKM), Department of Science and Technology, New Delhi
SR/S1/RFPC06/2006 | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | PERGAMON-ELSEVIER SCIENCE | en_US |
| dc.subject | ION PROMOTED REACTIONS | en_US |
| dc.subject | CONCISE SYNTHESIS | en_US |
| dc.subject | O-ANTIGEN | en_US |
| dc.subject | CELL-WALL | en_US |
| dc.subject | PRIMARY ALCOHOLS | en_US |
| dc.subject | PERGAMON-ELSEVIER SCIENCE | en_US |
| dc.title | Total synthesis of the heptasaccharide repeating unit of the iron-binding exopolysaccharide secreted by Klebsiella oxytoca BAS-10 | en_US |
| dc.title.alternative | TETRAHEDRON-ASYMMETRY | en_US |
| dc.type | Article | en_US |