𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Methyl 4-tert-butoxy­carbonyl-N-cyano­piperazine-1-carboximidothio­ate

✍ Scribed by Lan, Bi-Jian ;Guo, Peng ;Zou, Zhen-Guang ;Lu, Yin-Xiang

Publisher
International Union of Crystallography
Year
2005
Tongue
English
Weight
293 KB
Volume
61
Category
Article
ISSN
1600-5368

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Facile Synthesis of
ChemInform Abstract: Facile Synthesis of 4-((N-(tert-Butoxycarbonyl)amino)methyl)-7-N- (tert-butoxycarbonyl)-3-oxa-2,7-diazabicyclo[3.3.0]oct-1-ene.
✍ Ho-Jung Kang 📂 Article 📅 2001 🏛 John Wiley and Sons ⚖ 30 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

tert-Butyl 4-[2-(methoxy­carbonyl)­ethyl
tert-Butyl 4-[2-(methoxy­carbonyl)­ethyl]-3,5-di­methyl-1H-pyrrole-2-carboxyl­ate
✍ Ramos Silva, Manuela ;Matos Beja, Ana ;Paixão, José António ;Lopes, Susana H. ;C 📂 Article 📅 2005 🏛 International Union of Crystallography 🌐 English ⚖ 209 KB

In the solid state, the title compound, C 15 H 23 NO 4 , forms centrosymmetric dimers in which individual molecules are linked by intermolecular N-HÁ Á ÁO hydrogen bonds. The pyrrole ring is planar within 0.004 (9) A ˚.

(2S,4R)-1-Benzyl 2-tert-butyl 4-[N,N′-bi
(2S,4R)-1-Benzyl 2-tert-butyl 4-[N,N′-bis(tert-butyl­oxy­carbonyl)­hydrazino]-5-oxopyrrolidine-1,2-di­carboxyl­ate
✍ 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

(1R,3R)-Methyl 6-tert-butoxy­carbonyl­am
(1R,3R)-Methyl 6-tert-butoxy­carbonyl­amino-1,5-dioxo-2,3-di­hydro-5H-1,3-thia­zolo­[3,2-a]­pyridine-3-carboxyl­ate
✍ Seger, Harald ;Marsch, Michael ;Geyer, Armin ;Harms, Klaus 📂 Article 📅 2005 🏛 International Union of Crystallography 🌐 English ⚖ 139 KB

The absolute configuration has been determined for the title compound, C 14 H 18 N 2 O 6 S, a fluorescent dipeptide analogue, which can act as a rigid backbone chromophore in peptides. Intermolecular N-HÁ Á ÁO C hydrogen bonds [HÁ Á ÁO = 2.37 (2) A ˚] are observed in the crystal packing.