0 -(4-methyl-1,3-thiazol-5-yl)-2-oxo-2,3,2 0 0 0 ,3 0 0 0 ,5 0 0 0 ,6 0 0 0 ,7 0 0 0 ,7a 0 0 0 -octahydro-1Hindole-3-spiro-3'-1H-pyrrolizin-2 0 0 0 -yl]prop-2-en-1-one
A Crystallographic Study of a Highly Substituted Imidazolinone, (3S,4S,5R)-3-(((S)-4-((1H-Indol-3-yl)Methyl)-5-Oxo-4,5-Dihydro-1H-Imidazol-2-yl)Amino)-4-((Tert-Butyldimethylsilyl)Oxy)-5-Hydroxypiperidin-2-One
✍ Scribed by Sanjay Dutta; Sergey M. Dibrov; Cody J. Higginson; Thomas Hermann
- Publisher
- Springer
- Year
- 2011
- Tongue
- English
- Weight
- 259 KB
- Volume
- 41
- Category
- Article
- ISSN
- 1572-8854
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## Abstract magnified image One‐pot reaction of 3‐aryl‐5‐methyl‐1,3,4‐oxadiazolin‐2‐ones **1a‐g** with ethanolamine yielded the 4‐(2‐hydroxyethyl)‐2‐aryl‐5‐methyl‐2,4‐dihydro‐3__H__‐1,2,4‐triazolin‐3‐ones **2a‐g** which were converted to the azido compounds **6a‐g**. These azides on 1,3‐dipolar cy
Cycloaddition of a (−)-menthone-derived nitrone to racemic but-3-en-2-ol led to two spirobicyclic heterocycles, with opposite configurations at the C atom attached to the OH group. This paper describes the __R__ epimer of the 1-hydroxyethyl substituent in imidazoisoxazole C~17~H~30~N~2~O~3~, (I). Th