𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Di-tert-butyl 2-(tert-butyl­oxy­carbonyl­methoxy)­phenyl­imino­di­acetate

✍ Scribed by Rademeyer, Melanie ;Barkhuizen, David A. ;Maguire, Glenn E. M.


Publisher
International Union of Crystallography
Year
2003
Tongue
English
Weight
281 KB
Volume
59
Category
Article
ISSN
1600-5368

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


[2-(tert­-Butyl­carbonyl­methylamino)phe
✍ Raynal, Nicolas ;Amblard, Muriel ;Martinez, Jean ;Rolland, Marc 📂 Article 📅 2002 🏛 International Union of Crystallography 🌐 English ⚖ 282 KB

We present here the crystal structure of the title compound, C 14 H 19 NO 4 . It contains OÁ Á ÁHÐO and NÁ Á ÁHÐO hydrogen bonds, connecting the molecules into centrosymmetric dimers and into in®nite chains.

tert-Butyl di­phenyl­phosphinate
✍ Grice, I. Darren ;Jenkins, Ian D. ;Busfield, W. Ken ;Byriel, Karl A. ;Kennard, C 📂 Article 📅 2004 🏛 International Union of Crystallography 🌐 English ⚖ 174 KB

Single-crystal X-ray study T = 293 K Mean '(C±C) = 0.008 A Ê R factor = 0.039 wR factor = 0.142 Data-to-parameter ratio = 15.2 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.

2,3-Bis(2-tert-butyl­phenyl­imino)butane
✍ Ferreira, Leonardo C. ;Filgueiras, Carlos Alberto L. ;Hörner, Manfredo ;Visentin 📂 Article 📅 2006 🏛 International Union of Crystallography 🌐 English ⚖ 212 KB

In the title compound, C 24 H 32 N 2 , there is one half-molecule in the asymmetric unit, the other half being generated by inversion. All bond lengths and angles show normal values. The deviation from a planar arrangement can be attributed to non-classical hydrogen bonds and steric factors.

(2S,4R)-1-Benzyl 2-tert-butyl 4-[N,N′-bi
✍ Kaczmarek, Krzysztof ;Wolf, Wojciech M. ;Zabrocki, Janusz 📂 Article 📅 2005 🏛 International Union of Crystallography 🌐 English ⚖ 222 KB

The title compound, C 27 H 39 N 3 O 9 , is a key intermediate in the synthesis of novel -turn mimetics based on electrophilic amination of enantiomerically pure (S)-pyroglutamic acid. The molecule adopts an extended conformation which is not stabilized by either intra-or intermolecular hydrogen bond