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The present invention provide compounds, and pharmaceutical compositions thereof, encompassed by the formulae (I), (II) or (III). The present invention also provides methods for treating FAAH mediated disease, disorder or condition by administering a therapeutically effective amount of a provided compound of the formulae (I), (II) or (III), or a pharmaceutical composition thereof, to a patient in need thereof. Additionally, the present invention provides methods for inhibiting FAAH in a patient by administering a therapeutically effective amount of a compound of the formulae (I), (II) or (III), or a pharmaceutical composition thereof, to a patient in need thereof

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

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The present invention refers to double stimulating – sensitive oligomer amine boronic acid relates to, more particularly a predetermined number of cationic amine groups and phenyl […] thereto to a structure group containing, carbon dioxide (CO2 ) And these engaging each monosaccharide (mono it buys car leading) have the combined living body conditions similar neutral pH excellent sensitive groove not cytotoxic in addition, CO in blood2 Irritation to the blood sugar – sensitive assembly, a virtual channel number for drug delivery are encapsulated in various medical fields using integral living body ideal material biodegradable oligomer amine boronic acid (OAB) patch, natural amino acids and 3 – carboxylic […] method using a same number bath, and medicine uses are disclosed. (by machine translation)

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Metal catalyst and ligand design,
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A cis-selective hydrogenation of abundant aryl boronic acids and their derivatives catalyzed by rhodium cyclic (alkyl)(amino)carbene (Rh?CAAC) is reported. The reaction tolerates a variety of boron-protecting groups and provides direct access to a broad scope of saturated, borylated carbo- and heterocycles with various functional groups. The transformation is strategically important because the versatile saturated boronate products are difficult to prepare by other methods. The utility of the saturated cyclic building blocks was demonstrated by post-functionalization of the boron group.

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

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In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 4408-64-4, name is 2,2′-(Methylazanediyl)diacetic acid, introducing its new discovery. Formula: C5H9NO4

The four-membered oxetane ring has been increasingly exploited for its contrasting behaviors: its influence on physicochemical properties as a stable motif in medicinal chemistry and its propensity to undergo ring-opening reactions as a synthetic intermediate. These applications have driven numerous studies into the synthesis of new oxetane derivatives. This review takes an overview of the literature for the synthesis of oxetane derivatives, concentrating on advances in the last five years up to the end of 2015. These methods are clustered by strategies for preparation of the ring and further derivatization of preformed oxetane-containing building blocks. Examples of the use of oxetanes in medicinal chemistry are reported, including a collation of oxetane derivatives appearing in recent patents for medicinal chemistry applications. Finally, examples of oxetane derivatives in ring-opening and ring-expansion reactions are described.

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

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Boron chemistry has evolved to become one of the most diverse and applied fields in organic synthesis and catalysis. Various valuable reactions such as hydroborylations and Suzuki?Miyaura cross-couplings (SMCs) are now considered as indispensable methods in the synthetic toolbox of researchers in academia and industry. The development of novel sterically-and electronically-demanding C(sp3)?Boron reagents and their subsequent metal-catalyzed cross-couplings attracts strong attention and serves in turn to expedite the wheel of innovative applications of otherwise challenging organic adducts in different fields. This review describes the significant progress in the utilization of classical and novel C(sp3)?B reagents (9-BBN and 9-MeO-9-BBN, trifluoroboronates, alkylboranes, alkylboronic acids, MIDA, etc.) as coupling partners in challenging metal-catalyzed C(sp3)?C(sp2) cross-coupling reactions, such as B-alkyl SMCs after 2001.

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Metal catalyst and ligand design,
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The substitution of one inosine (Ino) with [Pd(II)(pac)(D2O)] complexes (pac = polyaminopolycarboxylate with pac = mida2-) and [Pd2(II)(pac)(D2O)2] (pac = hdta4- and egta4- produce products in which the entering Ino ligand resides trans to the iminodiacetate N donor and the two glycinato arms of the iminodiacetate donor have a ‘one on, and one off’ arrangement. Reactions were carried out in the pD range of 5.0 – 6.0 in order to assure that glycinato carboxylates would be coordinated in the starting [Pd(pac)(D2O)] complex and in a range such that the final coordination of inosine is favored at the N-7 donor site. The structure of the product was deduced from 1H and 13C NMR studies. These [Pd(pac)L] products are consistent with a common trigonal bipyramidal intermediate with the entering Ino group displacing an in-plane glycinato group. Substitution of one Ino on [Pd(II)(mida)Cl]- results in both glycinato donors being made pendant. A different, more square-pyramidal intermediate leads to this product whereas a TBP geometry will not. The tendency toward formation of stable bis [Pd(II)(pac)L2] products increases in the order of the pac ligand of 1/2 egta4- > 1/2 hdta4- > mida2-, indicating that strain at the central iminodiacetates’ nitrogen donor favors displacement of the second glycinato chelate, but that having binuclear Pd(II) centers too close disfavors forming bis-derivatized Pd(II) headgroups. Rather, the longer eight methylene equivalent spacer in [Pd2(egta)(H2O)2] compared to six methylenes in [Pd2(hdta)(H2O)2] allows for bis addition at both Pd(II) centers to proceed to completion. If the entering ligand is the anionically charged 5′-GMP nucleotide instead of the neutrally charged Ino, addition stops at the ‘one on, one off’ 1:1 complex per Pd(II) center with [Pd2(egta)(H2O)2], just as Ino addition to the anionically charged [Pd(mida)Cl]- stops at the first addition step. Two types of Pd(II) derivatized isomer are detected for the [Pd2(Ino)4(hdta)] complex, e.g. with Ino groups either trans or cis to each other. 31P NMR studies show that association of the phosphate ester unit of 5′-GMP or of H2PO4- make only transitory interactions with the Pd(II) center such that a rearrangement that is observed on a slow time scale of > 24 h for the decay of an unstable isomer of [Pd2(5′-GMP)2(egta)]2- must be due to an N-1 to N-7 rearrangement, rather than a phosphate ester coordination to N-4 migration. Likewise, unstable species are found by 1H NMR for Ino substitutions on [Pd(mida)Cl]- and [Pd2(hdta)(D2O)2]. The processes that alter the initial distribution of species are attributed to N-1 to N-7 isomerisms. The major substitution product for Ino or 5′-GMP, in all cases of Pd(pac) substitutions, is the N-7 coordinated purine nucleoside or nucleotide, as shown by 1H NMR parameters of the several species. In this manner, the behavior of Pd(II)(pac) coordination of purine nucleobases parallels the behavior of Pd(II)-dipeptide and tripeptide complexes in forming ternary complexes with DNA nucleobases. Both Pd(II)(pac) and Pd(II)(peptide) complexes have neutral or anionic reaction centers. In contrast, the cationic Pd(II)(dien) purine complexes favor N-1 coordination much more strongly, and are therefore poorer models of ternary protein-metal ion-DNA nucleobase interactions of importance in transcription processes and cytotoxic DNA-protein crosslinks. (C) 2000 Elsevier Science B.V.

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

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Oxidative degradation experiments on five amines and two amino acids were performed in a new closed setup at atmospheric pressure. For most of the amines/amino acids significant degradation was not present under these conditions, except for MEA and MMEA. The degradation compounds found seem to follow the same patterns as described in literature. Volatile compounds as ammonia and alkylamine play an important role in understanding the initial degradation mechanisms. For MMEA, methylamine and ammonia were found in the same order of magnitude. Oxygen stochiometry of the degradation compounds could not be explained by initial air in the system. Oxygen in some of the degradation compounds could come from oxygen diffusing into the system as seen from proposed model and/or water reacting with iminium giving aldehyde and amine/ammonia. Temperature and dissolved metal seemed to influence oxygen and degradation rate for the MEA experiments.

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Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

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Bis-acyl-/aroyl-hydrazones can be divided into two basic structural categories: those that are derived from a dihydrazide and those that are derived from a dialdehyde (or diketone). They form various types of complexes that are herein reviewed.

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Reference:
Metal catalyst and ligand design,
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Finding new methods of carbon-carbon bond formation is a key goal in expanding current methodology for heterocycle formation. Because of their inherently nonplanar shape, new methods of forming sp3-rich scaffolds are of particular importance. Although there are methods for combining heterocyclization and formation of new sp3-sp3 carbon-carbon bonds, these form the carbon-heteroatom bond rather than a carbon-carbon bond of the heterocycle. Here, we show a new alkene arylallylation reaction that generates a heterocycle with concomitant formation of two new carbon-carbon bonds. Furthermore, we demonstrate that this process occurs through an isohypsic (redox neutral) mechanism. Overall, this carboallylation reaction gives a new route to the synthesis of 3,3-disubstituted heterocycles.

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

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The dCTPase pyrophosphatase 1 (dCTPase) regulates the intracellular nucleotide pool through hydrolytic degradation of canonical and noncanonical nucleotide triphosphates (dNTPs). dCTPase is highly expressed in multiple carcinomas and is associated with cancer cell stemness. Here we report on the development of the first potent and selective dCTPase inhibitors that enhance the cytotoxic effect of cytidine analogues in leukemia cells. Boronate 30 displays a promising in vitro ADME profile, including plasma and mouse microsomal half-lives, aqueous solubility, cell permeability and CYP inhibition, deeming it a suitable compound for in vivo studies.

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI