Pressure-induced polymorphism in cyclopropylamine
نویسندگان
چکیده
منابع مشابه
High Pressure Polymorphism in Silica
Fundamental crystal chemistry and first-principles total-energy calculations are used to examine stable and metastable high-pressure silica structures. We find that a large class of energetically competitive phases can be generated from hcp arrays of oxygen with silicon occupying one-half of the octahedral sites. Calculations for specific structures provide an explanation for a number of recent...
متن کاملScalable synthesis of (1-cyclopropyl)cyclopropylamine hydrochloride
1-Cyclopropylcyclopropanecarboxylic acid (2), which is accessible on a large scale (900 mmol) from 1-bromo-1-cyclopropylcyclopropane (1) in 64% yield (89% on a 12.4 mmol scale), has been subjected to a Curtius degradation employing the Weinstock protocol to furnish the N-Boc-protected (1-cyclopropyl)cyclopropylamine 3 (76%). Deprotection of 3 with hydrogen chloride in diethyl ether gave the (1-...
متن کاملHigh pressure polymorphism of β-TaON.
The high pressure behavior of TaON was studied using a combination of Raman scattering, synchrotron X-ray diffraction, and X-ray absorption spectroscopy in diamond anvil cells to 70 GPa at ambient temperature. A Birch-Murnaghan equation of state fit for baddeleyite structured β-TaON indicates a high bulk modulus value Ko = 328 ± 4 GPa with K = 4.3. EXAFS analysis of the high pressure XAS data p...
متن کاملCyclopropylamine inactivation of cytochromes P450: role of metabolic intermediate complexes.
The inactivation of cytochrome P450 enzymes by cyclopropylamines has been attributed to a mechanism involving initial one-electron oxidation at nitrogen followed by scission of the cyclopropane ring leading to covalent modification of the enzyme. Herein, we report that in liver microsomes N-cyclopropylbenzylamine (1) and related compounds inactivate P450 to a large extent via formation of metab...
متن کاملtrans-2-(2,5-Dimethoxy-4-iodophenyl)cyclopropylamine and trans-2-(2,5-dimethoxy-4-bromophenyl)cyclopropylamine as potent agonists for the 5-HT2 receptor family
A strategy to replace the ethylamine side chain of 2,5-dimethoxy-4-iodoamphetamine (DOI, 1a), and 2,5-dimethoxy-4-bromoamphetamine (DOB, 1b) with a cyclopropylamine moiety was successful in leading to compounds with high affinity at the 5-HT(2) family of receptors; and the more potent stereoisomer of the cyclopropane analogues had the expected (-)-(1R,2S)-configuration. Screening for affinity a...
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ژورنال
عنوان ژورنال: Acta Crystallographica Section B Structural Science
سال: 2005
ISSN: 0108-7681
DOI: 10.1107/s0108768105026327