Optically active (R)-(+)-2, 2' -bis(2 -trifluoro-4 -aminophenoxy)- 1, 1' -binaphthyl was prepared from1, 1'-bi-2-naphthol. The optically active aromatic polyimide was also successfully synthesized. This ne...Optically active (R)-(+)-2, 2' -bis(2 -trifluoro-4 -aminophenoxy)- 1, 1' -binaphthyl was prepared from1, 1'-bi-2-naphthol. The optically active aromatic polyimide was also successfully synthesized. This newpolymer has good solubility, thermal stability etc. Its specific rotation was found to be +174°, and itschiroptical property was also studied.展开更多
This paper generally introduces the basic properties and applications of l, 1 - bi - 2 - naphthol. Especially the latest research and development on synthesis and resolution process of 1, 1 - bi - 2naphthol at home an...This paper generally introduces the basic properties and applications of l, 1 - bi - 2 - naphthol. Especially the latest research and development on synthesis and resolution process of 1, 1 - bi - 2naphthol at home and abroad was remarked.展开更多
A simple,highly effective hydrogenation of chiral BINOL to provide H_4-BINOL in multigram scale with good yield（up to 78% yield） was developed.A series of heterogeneous catalysts was tested in the hydrogenation;;the...A simple,highly effective hydrogenation of chiral BINOL to provide H_4-BINOL in multigram scale with good yield（up to 78% yield） was developed.A series of heterogeneous catalysts was tested in the hydrogenation;;the best result was obtained with 5%Pd/ C in EtOH under the H_2 pressure of 50 bar for 2 h.This method is a more useful method for practical synthesis of optically pure H4- BINOL than other available methods.展开更多
By capitalizing on the capability of photoredox catalysis to generate reactive radical intermediate under mild conditions, we established a photocatalytic cross-coupling protocol that could deliver both derivatives fr...By capitalizing on the capability of photoredox catalysis to generate reactive radical intermediate under mild conditions, we established a photocatalytic cross-coupling protocol that could deliver both derivatives from 1-bromo-2-naphthols in combination with 2-naphthols or 2-naphthylamines. This distinct activation mode could overcome structural or electronic limitation associated with conventional coupling pathways. Additionally, a novel kinetic resolution protocol of unprotected BINOLs has been established with azodicarboxylates via chiral phosphoric acid(CPA) catalysis. Selectivity factor of up to 175 could be achieved and delivered to both enantiomers in atropisomerically enriched form after a simple work-up.展开更多
基金This project was supported by National Natural Science Foundation of China.
文摘Optically active (R)-(+)-2, 2' -bis(2 -trifluoro-4 -aminophenoxy)- 1, 1' -binaphthyl was prepared from1, 1'-bi-2-naphthol. The optically active aromatic polyimide was also successfully synthesized. This newpolymer has good solubility, thermal stability etc. Its specific rotation was found to be +174°, and itschiroptical property was also studied.
文摘This paper generally introduces the basic properties and applications of l, 1 - bi - 2 - naphthol. Especially the latest research and development on synthesis and resolution process of 1, 1 - bi - 2naphthol at home and abroad was remarked.
基金supported by the Science and Technology Department of Zhejiang Province(no.2008C21041)was partially supported by the NSFC(no.20572101)
文摘A simple,highly effective hydrogenation of chiral BINOL to provide H_4-BINOL in multigram scale with good yield（up to 78% yield） was developed.A series of heterogeneous catalysts was tested in the hydrogenation;;the best result was obtained with 5%Pd/ C in EtOH under the H_2 pressure of 50 bar for 2 h.This method is a more useful method for practical synthesis of optically pure H4- BINOL than other available methods.
基金supported by the National Natural Science Foundation of China (21825105)the Guangdong Provincial Key Laboratory of Catalysis (2020B121201002)+3 种基金the Guangdong Innovative Program (2019BT02Y335)the Shenzhen Special Funds (JCYJ20190812-112603598, JCYJ20210324120205016)the Shenzhen Nobel Prize Scientists Laboratory Project (C17213101)the SUSTech Special Fund for the Construction of High-Level Universities (G02216302)。
文摘By capitalizing on the capability of photoredox catalysis to generate reactive radical intermediate under mild conditions, we established a photocatalytic cross-coupling protocol that could deliver both derivatives from 1-bromo-2-naphthols in combination with 2-naphthols or 2-naphthylamines. This distinct activation mode could overcome structural or electronic limitation associated with conventional coupling pathways. Additionally, a novel kinetic resolution protocol of unprotected BINOLs has been established with azodicarboxylates via chiral phosphoric acid(CPA) catalysis. Selectivity factor of up to 175 could be achieved and delivered to both enantiomers in atropisomerically enriched form after a simple work-up.
