An eco-friendly,sustainable, and greener approach to the synthesis of Dihydroquinazolin-4(1H)-ones using a deep eutectic solvent

A safer, greener, and more effective reaction methodology for the synthesis of dihydroquinazolinones (DHQs) has been developed. The deep eutectic solvent (DES) ZnCl₂/urea employed in this study efficiently accelerated the cyclization of 2-aminobenzamide with different aldehydes (aromatic and heteroaromatic) to afford the target scaffolds without the generation of any oxidized product. This method has exhibited remarkable advantages such as quick reaction time, mild reaction conditions, high yield (82%–98%), operational simplicity, and selectivity. The approach was observed to be tolerant to electron-donating and electron-withdrawing functional groups. Green metric parameters (AEf, OE, AE, RME, CE, etc.) determined further aided this greener chemical approach.     

Weighted composition operators between weighted spaces of vector-valued holomorphic functions on Banach spaces

Let B(E, F) be the Banach Space of all continuous linear operators from a Banach Space E into a Banach space F. Let U_X and U_Y be balanced open subsets of Banach spaces X and Y, respectively. Let V and W be two Nachbin families of continuous weights on U_X and U_Y, respectively. Let HV(U_X, E) (or HV₀(U_X, E)) and HW(U_Y, F) (or HW₀(U_Y, F)) be the weighted spaces of vector-valued holomorphic functions. In this paper, we investigate the holomorphic mappings ? : U_Y → U_X and ψ : U_Y → B(E, F) which generate weighted composition operators between these weighted spaces.     

Enantiospecific synthesis of β-lactams via cycloaddition

Enantiospecific synthesis of variously substituted cis-β-lactams can be achieved by the annelation of Schiff bases from optically active ketal aldehydes derived from D-threonine. Similar annelation of Schiff bases from the triphenylsilyl ether of D-threonine ester and cinnamaldehyde leads to cis-β-lactams with high diastereofacial selectivity.     

Heterocyclic compounds. VII. Synthesis of thiadiazasteroid analogs

The synthesis of a number of β-northiadiaza steroid analogs has been described. Suitable o-aminonitriles were acylated with γ-chlorobutyryl chloride. These amidonitriles were cyclized to substituted γ-lactams and subsequently to the tetracyclic products. To functionalize the “17-position” in these steroids, the intermediate γ-lactams were converted to arylidene derivatives before cyclization to the tetracyclic derivatives.     

Heterocyclic compounds. X. A new synthesis of thiadiazasteroids

The reaction of ν-ketoacids or ν-aldehydo acids with o-amino amides results in the formation of 4-quinazolones. Using this reaction a number of polyheterosteroid analogs were synthesized. Thus, when 2-amino-3-carboxamido-4,5,6,7-tetrahydrobenzothiophene (9) was refluxed with levulinic acid (10) in a high boiling solvent, thiadiazasteroid analog (11) was obtained in 78% yield. It was found that this facile one-step reaction could be used to synthesize a variety of tetra and pentacyclic compounds. Nmr spectroscopy was used to assign stereochemistry to the 17-methyl “steroids” (31) and (32).     

Quantitative determination of four constituents of Tinospora sps. by a reversed-phase HPLC-UV-DAD method. Broad-based studies revealing variation in content of four secondary metabolites in the plant from different eco-geographical regions of India

This paper describes the separation and quantitation of important markers, such as 20beta-hydroxyecdysone, tinosporaside, cordioside, and columbin, present in three species of Tinospora viz, T. cordifolia, T. malabrica, and T. crispa. A reverse-phase (RP) high-performance liquid chromatography (HPLC)-UV-diode array detection (DAD) method employing gradient elution is thus developed. The marker compounds isolated from 70% ethanolic extract of T. cordfolia by repeated column chromatography are identified on the basis of (1)H NMR, (13)C NMR, and mass spectral data. The compounds are separated on a RP (RP-18, 5 microm, 250 x 4.6-mm i.d.) column using water-acetonitrile gradient and are detected by the HPLC-UV-DAD method. The calibration curves that result from marker compounds in the concentration range of 100-2000 ng on column exhibit a good correlation (r(2) > or = 0.99978). The method is successfully applied to separate and study the content of four marker compounds in 40 different accessions of three Tinospora species collected from different regions of India. The studies reveal that the maximum amount of the marker compounds is present in Tinospora cordifolia species, especially from accessions collected from higher altitudes of the Jammu province (North India).