Asymmetric synthesis of polyhydroxylated pyrrolizidines via transannular iodoamination with concomitant N-debenzylation

The doubly diastereoselective "matched" conjugate addition of lithium (R)-N-but-3-enyl-N-(α-methyl-p-methoxybenzyl)amide to tert-butyl (4S,5R,E)-4,5-O-isopropylidene-2,7-dienoate (derived from d-ribose in 3 steps) and in situ enolate oxidation with (-)-camphorsulfonyloxaziridine was followed by ring-closing metathesis with Grubbs I to give a hexahydroazocine scaffold. Subsequent treatment with I(2) resulted in transannular iodoamination accompanied by loss of the α-methyl-p-methoxybenzyl group to give the corresponding pyrrolizidine scaffold as a single diastereoisomer upon direct crystallization from the crude reaction mixture. Further functional group manipulations enabled the preparation of (-)-7a-epi-hyacinthacine A1.     

Marrying iterative synthesis to cascading radical cyclization: 6-endo/5-exo radical cascade across bis-vinyl ethers

Application of iterative protocols to the synthesis of functionally and stereochemically complex small molecules is an emerging area of research with the potential to create new efficiencies in complex molecule synthesis. Similarly, the discovery of tandem or cascade reactions can aid in the rapid generation of new structures for biological screening programs. This report describes a cascading 6-endo-trig/5-exo-trig radical cyclization across bis-vinyl ether substrates, which are themselves iteratively synthesized from simple building blocks.     

Highly diastereoselective and stereodivergent dihydroxylations of acyclic allylic amines: application to the asymmetric synthesis of 3,6-dideoxy-3-amino-L-talose

Aminohydroxylation of tert-butyl sorbate [tert-butyl (E,E)-hexa-2,4-dienoate] using enantiopure lithium (R)-N-benzyl-N-(α-methylbenzyl)amide and (-)-camphorsulfonyloxaziridine gives tert-butyl (R,R,R,E)-2-hydroxy-3-[N-benzyl-N-(α-methylbenzyl)amino]hex-4-enoate in >99:1 dr. Subsequent dihydroxylation under Upjohn conditions (OsO(4)/NMO) gives tert-butyl (2R,3R,4S,5S,αR)-2,4,5-trihydroxy-3-[N-benzyl-N-(α-methylbenzyl)amino]hexanoate (in 95:5 dr) while dihydroxylation under Donohoe conditions (OsO(4)/TMEDA) proceeds with antipodal diastereofacial selectivity to give the (R,R,R,R,R)-diastereoisomer (in 95:5 dr). The amino triols resulting from these dihydroxylation reactions are useful for further elaboration, as demonstrated by the asymmetric synthesis of 3,6-dideoxy-3-amino-L-talose.     

D2-symmetric dirhodium catalyst derived from a 1,2,2-triarylcyclopropanecarboxylate ligand: design, synthesis and application

Dirhodium tetrakis-(R)-(1-(4-bromophenyl)-2,2-diphenylcyclopropanecarboxylate) (Rh(2)(R-BTPCP)(4)) was found to be an effective chiral catalyst for enantioselective reactions of aryl- and styryldiazoacetates. Highly enantioselective cyclopropanations, tandem cyclopropanation/Cope rearrangements and a combined C-H functionalization/Cope rearrangement were achieved using Rh(2)(R-BTPCP)(4) as catalyst. The advantages of Rh(2)(R-BTPCP)(4) include its ease of synthesis, its tolerance to the size of the ester group in the styryldiazoacetates, and its compatibility with dichloromethane as solvent. Computational studies suggest that the catalyst adopts a D(2)-symmetric arrangement, but when the carbenoid binds to the catalyst, two of the p-bromophenyl groups on the ligands rotate outward to make room for the carbenoid and the approach of the substrate to the carbenoid.     

The effect of dipole moment and electron deficiency of analytes on the chemiresistive response of TiO2(B) nanowires

Nanostructured TiO(2)(B) thin films were found to have strong and fast chemiresistive response to nitro-aromatic and nitro-amino explosives recently. In this study, the effects of dipole moment and electron deficiency of the analyte molecules on the chemiresistive response are explored to understand the details of molecular interactions of analytes with the sensor surface which lead to charge depletion and the chemiresistive effect. It was found that the speed of the response is dominated by the polarity of the analytes and molecules with larger dipole moments produce faster responses. The degree of the response was found to be dominated by the electron deficiency of the analytes and molecules with greater electron deficiency produce stronger chemiresistive responses.     

Rh2(S-PTAD)4-catalyzed asymmetric cyclopropenation of aryl alkynes

Rh₂(S-PTAD)₄ is an effective catalyst for the asymmetric cyclopropenation of aryl alkynes using a siloxyvinyldiazoacetate as the carbenoid precursor. Upon deprotection of the silyl protecting group, highly enantioenriched cyclopropenes bearing geminal acceptor groups can be accessed. These cyclopropenes undergo regioselective rhodium(II)-catalyzed ring expansion to furans.     

Preparative scale synthesis of the biaryl core of anacetrapib via a ruthenium-catalyzed direct arylation reaction: unexpected effect of solvent impurity on the arylation reaction

In this report, we disclose our findings regarding the remarkable effect of a low-level impurity found in the solvent used for a ruthenium-catalyzed direct arylation reaction. This discovery allowed for the development of a robust and high-yield arylation protocol that was demonstrated on a multikilogram scale using carboxylate as the cocatalyst. Finally, a practical, scalable, and chromatography-free synthesis of the biaryl core of Anacetrapib is described.     

Optimization of the Hartmann-Shack microlens array

In this work we propose to optimize the microlens-array geometry for a Hartmann-Shack wavefront sensor. The optimization makes possible that regular microlens arrays with a larger number of microlenses are replaced by arrays with fewer microlenses located at optimal sampling positions, with no increase in the reconstruction error. The goal is to propose a straightforward and widely accessible numerical method to calculate an optimized microlens array for a known aberration statistics. The optimization comprises the minimization of the wavefront reconstruction error and/or the number of necessary microlenses in the array. We numerically generate, sample and reconstruct the wavefront, and use a genetic algorithm to discover the optimal array geometry. Within an ophthalmological context, as a case study, we demonstrate that an array with only 10 suitably located microlenses can be used to produce reconstruction errors as small as those of a 36-microlens regular array. The same optimization procedure can be employed for any application where the wavefront statistics is known.     

The scope of ambiphilic acetate-assisted cyclometallation with half-sandwich complexes of iridium, rhodium and ruthenium

C? H activation by acetate‐assisted cyclometallation of a phenyl group with half‐sandwich complexes [{MCl₂Cp*}₂] (M=Ir, Rh) and [{RuCl₂(p‐cymene)}₂] can be directed by a wide range of nitrogen donor ligands including pyrazole, oxazoline, oxime, imidazole and triazole, and X‐ray structures of a number of complexes are reported. All the ligands tested cyclometallated at iridium, however ruthenium and rhodium fail to cause cyclometallation in some cases. As a result, the nitrogen donors have been categorised based on their reactivity with the three metals used. The relevance of these cyclometallation reactions to catalytic synthesis of carbocycles and heterocycles is discussed.     

Strength of free-standing chemically vapour-deposited diamond measured by a range of techniques

The strength of free-standing chemically vapour-deposited diamond was determined using a bursting-disc test, a three-point bend test and a four-point bend test. The bursting-disc technique has advantages for determining the strength of ceramic materials since the maximum tensile stress is at the centre of the disc. The much smaller stresses near the sample edges are rarely responsible for failure and so edge effects are negligible. However, the bursting-disc test is often impractical for ascertaining the strength of chemically vapour-deposited diamond since the cost of samples is high. A three-point bend test is often employed instead, since it may be performed on smaller samples. However, the area stressed in the three-point bend test is smaller, and so there is less chance of stressing a large flaw, resulting in higher strength values. A further disadvantage is that specimen edges are stressed and, unless the specimen sides are polished, as well as its faces, misleading results may be obtained (although this is not the case for chemically vapour-deposited diamond). A four-point bend test is often used because it stresses a larger volume of material than the three-point bend test and so the results are more reliable. Furthermore, the diamond used in a four-point bend test can be of similar size to those used in a three-point bend test and so the expenditure is comparable. However, ensuring that the four-point bend test is applied correctly is technically more difficult. Strength data are reported for both the growth and the nucleation sides, for difference nucleation densities and for as-received and polished samples.