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https://hdl.handle.net/10356/96150
Title: | Asymmetric hydroarsination reactions toward synthesis of alcohol functionalised C-chiral As–P ligands promoted by chiral cyclometallated complexes | Authors: | Cheow, Yuen Lin Li, Yongxin Leung, Pak-Hing Pullarkat, Sumod A. |
Keywords: | DRNTU::Science::Chemistry::Organic chemistry::Organometallic compounds | Issue Date: | 2012 | Source: | Cheow, Y. L., Pullarkat, S. A., Li, Y., & Leung, P.-H. (2012). Asymmetric hydroarsination reactions toward synthesis of alcohol functionalised C-chiral As–P ligands promoted by chiral cyclometallated complexes. Journal of organometallic chemistry, 696(26), 4215-4220. | Series/Report no.: | Journal of organometallic chemistry | Abstract: | The asymmetric hydroarsination reactions between diphenylarsine and 3-diphenylphosphanyl-but-3-en-1-ol and 2-diphenylphosphanyl-prop-2-en-1-ol have been achieved using the organopalladium complex containing ortho-metallated (R)-[1-(dimethylamino)ethylnaphthalene as the chiral reaction template in high stereoselectivities under mild conditions. Hydroarsination of 3-diphenylphosphanyl-but-3-en-1-ol with diphenylarsine generated only one stereoisomer as five-membered As–P bidentate chelate on chiral naphthylamine palladium template. Using the same chiral metal template, similar hydroarsination reaction was carried out on 2-diphenylphosphanyl-prop-2-en-1-ol which gave two different products in the ratio of 2.6 to 1. The major isomer was identified as the expected five-membered As–P bidentate ligand and the minor isomer was identified as the elimination product. The naphthylamine auxiliary could be removed chemoselectively by treatment with concentrated hydrochloric acid. Optically pure As–P ligands containing the hydroxy groups at the chiral carbon centres were prepared by ligand displacement. The absolute configuration and coordination properties of the complexes have been established by single crystal X-ray analysis. | URI: | https://hdl.handle.net/10356/96150 http://hdl.handle.net/10220/17145 |
ISSN: | 0022-328X | DOI: | 10.1016/j.jorganchem.2011.09.016 | Schools: | School of Physical and Mathematical Sciences | Fulltext Permission: | none | Fulltext Availability: | No Fulltext |
Appears in Collections: | SPMS Journal Articles |
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