86980-83-8Relevant academic research and scientific papers
OPTISCH AKTIVE UEBERGANGSMETALL-KOMPLEXE. LXXXIII. KONFIGURATIONSSTABILE TETRAEDRISCHE NiNi'CC'-CLUSTER
Brunner, Henri,Muschiol, Manfred
, p. 233 - 239 (1983)
The reaction of Ni(C5H5)2 and Ni(C5H4COOCH3)2 with the acetylene (-)-(R)-C6H5CCCONHCH(CH3)(C6H5), "CC'", yields tetrahedral Ni2C2 clusters.Besides the compounds with two identical Ni corners (Ni2CC' types) also compounds with two different Ni corners (NiNi'CC' types) are formed.These consist of two diastereomers which, for a given (R)-configuration in the acid amide substituent, differ only in the cluster chirality.They are separated chromatographically and turn out to be configurationally stable with respect to a change of the cluster chirality.
Alkynylboration Reaction Leading to Boron-Containing π-Extended cis-Stilbenes as a Highly Tunable Fluorophore
Nogami, Marina,Hirano, Keiichi,Morimoto, Kensuke,Tanioka, Masaru,Miyamoto, Kazunori,Muranaka, Atsuya,Uchiyama, Masanobu
supporting information, p. 3392 - 3395 (2019/05/10)
An unprecedented boron-containing fluorophore, π-extended cis-stilbene, obtained via alkynylboration reaction of alkynamide is reported. Boron-containing π-extended cis-stilbenes emit fluorescence with high quantum yields in the solid state and exhibit aggregation-induced emission enhancement. The broad substrate scope of the alkynylboration reaction offers facile access to electronically diverse structures, enabling fine-tuning of light absorption/emission characteristics. The boron-containing π-extended cis-stilbene with a diphenylamino group displays solvatofluorochromism via an intramolecular charge-transfer transition.
Intermolecular asymmetric carboesterification of alkenes by using chiral amine auxiliaries under o2: Synthesis of enantioenriched α-methylene-γ-lactones through chloropalladation of alkynes
Zhang, Zhenming,Wu, Wanqing,Liao, Jianhua,Li, Jianxiao,Jiang, Huanfeng
supporting information, p. 6708 - 6712 (2015/04/27)
Herein, the first example of chloropalladation-initiated asymmetric intermolecular carboesterification of alkenes with alkynes by using chiral amine auxiliaries is reported. The use of (1S,2S)-N1,N1-dimethylcyclohexane-1,2-diamine auxiliaries is essential for providing α-methylene-γ-lactones products in moderate to high yields and excellent enantioselectivities at room temperature. Moreover, the chiral amine auxiliaries can be readily removed by hydrolysis during the reaction process to keep the absolute configuration. This oxygen- and water-promoted asymmetric reaction opens a new window to study asymmetric processes in halopalladation reactions.
