[3+2] Cycloadditions. Part XXXIII. Selective cycloadditions of C-(1-naphthyl)-N-methyl nitrone and C-phenyl-N-benzyl nitrone to α,β-unsaturated carbonyl compounds1,2

488-501[3+2] Cycloadditions [32CA] involving nitrones as 1,3-dipolar species to alkenes yield isoxazolidines, which on further transformations can be converted to naturally occurring bioactive compounds. Thus the 32CA route provides conversion of simple natural products to more complex natural occurring bioactive nitrogen heterocycles, and close analogues. The present work deals with 32CA between the nitrones C-(1-naphthyl)-N-methyl nitrone and C-phenyl-N-benzyl nitrone to α,β-unsaturated carbonyl compounds as dipolarophiles, viz. arylidene malonate esters, methyl cinnamate and benzylidene acetophenone (chalcone). Methyl cinnamate is a naturally occurring compound, while the chalcone scaffold is present in several natural products. Structure elucidation of the generated cycloadducts have been achieved by means of detailed spectroscopic and XRD studies. All the cycloadditions investigated occurr regioselectively to yield tetra/penta-substituted isoxazolidines, where the carbonyl group(s) are situated at the 4-position of the isoxazolidine ring. DFT computations including optimised geometries, FMO energies, electronic chemical potentials, chemical hardness, chemical softness and reactivity indices of a number of the reactants have been calculated at DFT/B3LYP/6-31++G(d,p) level of theory. The calculated reactivity indices have been used to analyse the 32CAs studied and to predict the regioselectivities; the predictions are in excellent accord with the experimental results

Tin (IV) chloride catalysed synthesis of di(indolyl)methanes during electrophilic substitution of indoles and 2-methyl indoles

An efficient methodology has been developed for the synthesis of di(indolyl)methanes in moderate to good yields during the study of the reactions of indole and 2-methyl indole using a series of aliphatic ketones in the presence of stannic chloride. It appears worth mentioning that with 2-methyl indole and acetone and ethyl methyl ketone the highly “elusive” indolylcarbinols, the postulated intermediates in the synthesis of di(indolyl)methanes, have been isolated

An Overview of the Genus Nardostachys

Nardostachys jatamansi, a medicinally important herb of Nepalese origin, has been used for centuries in the Ayurvedic and Unani systems of medicine. In combination with Marsilea minuta it is being used as an antistress and anticonvulsant drug and also finds use in the treatment of epilepsy. Recently, it has been reported that N. jatamansi, which plays an important role in protecting from cerebral ischemia and liver damage, is also used for the treatment of osteoporosis and hypercalcemia. The other member of the genus Nardostachys, N. chinensis, possesses antifungal and antimalarial properties. It is also used in the treatment of skin dysfunction. A short summary of the chemical constituents of the two species along with their physical and biological properties is reported

N-(4-Methylphenyl) Benzenepropanamide - the First Isolated Amide From the Genus Paederia

Investigation of the stem of Paederia foetida (Rubiaceae) resulted in the isolation and characterization of N-(4-methylphenyl)-benzopropanamide, which was hitherto unknown as a natural product This is the first report of an amide for the genus Paederia

New synthesis of (+) 2,3-dimethoxyhexahydroberbine

121-12

Electrophilic substitution. reactions of indoles: Part XVIII - Further investigation on the synthesis of benzazepinone skeleton

761-76

1,3-Dipolar cycloadditions: Part III-Cycloaddition of C,N-diarylnitrones to N-cinnamoylpiperidines

105-11

A new dimeric coumarin from Boenninghausenia albiflora Reichb and Meissner (Rutaceae)

523-52

Evaluation of the Edinburgh Post Natal Depression Scale using Rasch analysis

BACKGROUND: The Edinburgh Postnatal Depression Scale (EPDS) is a 10 item self-rating post-natal depression scale which has seen widespread use in epidemiological and clinical studies. Concern has been raised over the validity of the EPDS as a single summed scale, with suggestions that it measures two separate aspects, one of depressive feelings, the other of anxiety. METHODS: As part of a larger cross-sectional study conducted in Melbourne, Australia, a community sample (324 women, ranging in age from 18 to 44 years: mean = 32 yrs, SD = 4.6), was obtained by inviting primiparous women to participate voluntarily in this study. Data from the EPDS were fitted to the Rasch measurement model and tested for appropriate category ordering, for item bias through Differential Item Functioning (DIF) analysis, and for unidimensionality through tests of the assumption of local independence. RESULTS: Rasch analysis of the data from the ten item scale initially demonstrated a lack of fit to the model with a significant Item-Trait Interaction total chi-square (chi Square = 82.8, df = 40; p < .001). Removal of two items (items 7 and 8) resulted in a non-significant Item-Trait Interaction total chi-square with a residual mean value for items of -0.467 with a standard deviation of 0.850, showing fit to the model. No DIF existed in the final 8-item scale (EPDS-8) and all items showed fit to model expectations. Principal Components Analysis of the residuals supported the local independence assumption, and unidimensionality of the revised EPDS-8 scale. Revised cut points were identified for EPDS-8 to maintain the case identification of the original scale. CONCLUSION: The results of this study suggest that EPDS, in its original 10 item form, is not a viable scale for the unidimensional measurement of depression. Rasch analysis suggests that a revised eight item version (EPDS-8) would provide a more psychometrically robust scale. The revised cut points of 7/8 and 9/10 for the EPDS-8 show high levels of agreement with the original case identification for the EPDS-10

Updated Guidance Regarding The Risk ofAllergic Reactions to COVID-19 Vaccines and Recommended Evaluation and Management: A GRADE Assessment, and International Consensus Approach

This guidance updates 2021 GRADE (Grading of Recommendations Assessment, Development and Evaluation) recommendations regarding immediate allergic reactions following coronavirus disease 2019 (COVID-19) vaccines and addresses revaccinating individuals with first-dose allergic reactions and allergy testing to determine revaccination outcomes. Recent meta-analyses assessed the incidence of severe allergic reactions to initial COVID-19 vaccination, risk of mRNA-COVID-19 revaccination after an initial reaction, and diagnostic accuracy of COVID-19 vaccine and vaccine excipient testing in predicting reactions. GRADE methods informed rating the certainty of evidence and strength of recommendations. A modified Delphi panel consisting of experts in allergy, anaphylaxis, vaccinology, infectious diseases, emergency medicine, and primary care from Australia, Canada, Europe, Japan, South Africa, the United Kingdom, and the United States formed the recommendations. We recommend vaccination for persons without COVID-19 vaccine excipient allergy and revaccination after a prior immediate allergic reaction. We suggest against \u3e 15-minute postvaccination observation. We recommend against mRNA vaccine or excipient skin testing to predict outcomes. We suggest revaccination of persons with an immediate allergic reaction to the mRNA vaccine or excipients be performed by a person with vaccine allergy expertise in a properly equipped setting. We suggest against premedication, split-dosing, or special precautions because of a comorbid allergic history