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http://nopr.niscpr.res.in/handle/123456789/16582Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Mashraqui, Sabir H | - |
| dc.contributor.author | Biswas, Maloyesh M | - |
| dc.date.accessioned | 2013-03-29T11:32:38Z | - |
| dc.date.available | 2013-03-29T11:32:38Z | - |
| dc.date.issued | 1999-08 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/16582 | - |
| dc.description | 959-961 | en_US |
| dc.description.abstract | The known 6-methoxymethyl-2-methylbenzothiazole 6 has been converted into quaternary ammonium hydroxide 4 via demethoxy-bromination followed by quaternization with (CH3)3N and treatment with silver oxide. Pyrrolysis of 4, expected to generate both anti-1 and syn-[2.2](2.6) benzothiazolophane 2 via 10π-10π couplings of the quinodimethane intermediate 5, gives in practice only anti-benzothiazolophane 1. The structure has been established by comparison with an authentic sample of 1 recently synthesized by an unambigous route. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | NISCAIR-CSIR, India | en_US |
| dc.rights |  CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
| dc.source | IJC-B Vol.38B(08) [August 1999] | en_US |
| dc.title | Synthesis of anti-[2.2](2.6)benzothiazolophane via 10π-10π: coupling protocol | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.38B(08) [August 1999] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 38B(8) 959-961.pdf | 1.51 MB | Adobe PDF | View/Open |
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