The thia-zolidine ring and the pyrrolidine ring in the title compound, C(25)H(26)N(2)O(2)S, both adopt an envelope conformation. The seven-membered ring has a twist-chair conformation. The crystal packing is stabilized by inter-molecular N-H⋯O hydrogen bonds.

Efficient and sustainable Buchwald-Hartwig amination enables the synthesis of new branched polymeric HTL materials for perovskite solar cells with performances comparable those Spiro-OMeTAD.

The Scaps-1d simulator was used to simulate a lead-free perovskite CH3NH3SnI3 based solar cell devices fabricated from different hole transport materials (HTM). This research looks at two organic and inorganic HTM layers. structure in this study is FTO/TiO2/CH3NH3SnI3/HTM (variable)/Au(variable). Spiro-OMeTAD, PEDOT:PSS, CuO Cu2O are the used. results show that utilizing as an produces better o...

Treatment of 2,2'-bis(allyloxy)-1,1'-binaphthyls with the first-generation Grubbs' carbene under MW-irradiation results in the formation of new polycyclic spiro-enones through an unprecedented RCM/Claisen sequence.

A direct and facile synthesis of highly functional 5-aza-spiro[2,4]heptanes, a valuable structural motif for drug discovery, is developed via catalytic asymmetric 1,3-dipolar cycloaddition of cyclopropylidene acetate and azomethine ylides for the first time.

A novel class of tartaric acid-derived N-spiro quaternary ammonium salts was synthesised starting from known TADDOLs. These compounds were found to catalyse the asymmetric α-alkylation of glycine Schiff bases with high enantioselectivities and in good yields.

The reaction of titanium cyclopropylidene complexes, prepared by the reductive titanation of 7,7-dichlorobicyclo[4.1.0]heptanes, with alkynes produced air and moisture stable titanacyclobutenes with a spiro-bonded cyclopropane.

An organocatalysis strategy has been developed toward the synthesis of O-spiro-C-aryl glycosides with different configurations in the sugar part. This strategy has been extended to the synthesis of the Papulacandin class of compounds.

A diastereoselective access to β-lactam fused spirocyclic oxindoles and related compounds bearing all carbon spiro centers is described. This N-heterocyclic carbene-catalyzed process employed challenging β,β-disubstituted α,β-unsaturated imines to react with enals.

The single crystals of a closed form spirooxazine spiro[azahomoadamantane-isoquinolinoxazine] were found for the first time to undergo photocoloration processes consistent with photochromism in the single crystalline phase.