## Abstract The synthesis of a chiral isocyanide possessing the easily cleaved menthoxy group is reported. Β© 2001 John Wiley & Sons, Inc. Heteroatom Chem 12:561β562, 2001
Long-distance chirality transfer in polymerization of isocyanides bearing a remote chiral group
β Scribed by Chen, Jian Ping; Gao, Jian Ping; Wang, Zhi Yuan
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 245 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0959-8103
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β¦ Synopsis
A long-distance chirality transfer was observed in the Ni(II)-catalysed polymerization of 5,6,9,10-tetrahydro[5]helicene-and [5]helicene-based isocyanides bearing a remote chiral group.
imide, which are laevorotatory, a β orded optically active polyisocyanides having dextrorotations at 589 nm and circular dichroism exciton couplets in the UV/vis. region. The chirality transfer from the remote stereogenic centre to the reactive isocyanido group was responsible for the helix-sense-selective polymerization.
π SIMILAR VOLUMES
## Abstract A diad compound 3Ξ²(bicyclo[2,2,1]heptaβ2,5βdieneβ2βmethylcarboxylateβ3βcarboxy)βanβdrostβ5βenβ17βone (NBDβSβONE) was synthesized and its photochemistry was examined. Irradiation of NBDβSβONE in acetonitrile at Ξ» > 300 nm selectively excited the keto chromophore. After intersystem crossi