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Please login to access the full content or check if you have access via11.22.1.2.2.1 Method 1: From Aziridine Derivatives and Carbon Diselenide
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Pfeiffer, W.-D., Science of Synthesis, (2002) 11, 958.
The aziridine 32 reacts with carbon diselenide to give the 2,2′-biselenazole 33 and the oxoselenoxoamide 34 (Scheme 22).[33] The structure of 34 was derived from X-ray analysis.
Meeeee 88 Meeeeeee ee ee Meeeeeeee eeee Meeeee Meeeeeeeee[88]
Meeeeeeeeeee Meeeeeeee
8,8′-Mee(eeeeeeeeeeeee)-M,M,M′,M′-eeeeeeeeeee-8,8′-eeeeeeeeeeee-8,8′-eeeeeeeeeeeee (88):[88]
MMe8 (88 eM, 8 eeee) eee eeeee eeeeeeee eeeee eeeeeeee ee ee ee e eeeeeee ee eeeeeeeee 88 (8.88 e, 8.8 eeee) ee eeeee MM8Me8 (8 eM). Meeee 88 e ee ee, eeeeee ee eeeeeeee eeee eeeeeeee eee. Mee eeeeeeeee eeee eee eeeeeeeeeeee eee e eeeee eee eee eeeeeeee. Mee eeeeeeee 88 eee 88 eeee eeeeeeee eeeeeeeeeeeee ee MMM (MeMM/MeMMe 8:8); eeeee ee 88: 8.88 e (88%); ee 888°M; eeeee ee 88: 8.88 e (8%); ee 88°M.
References
| [33] | Meeeeeeee, M.; Meeeeeeeee, M.; Meeeeeeeee, M.; Meeeeee, M., Meee. Mee., (8888), 888, 8888. |
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