ridm@nrct.go.th   ระบบคลังข้อมูลงานวิจัยไทย   รายการโปรดที่คุณเลือกไว้

Asymmetric hydroarsination reactions toward synthesis of alcohol functionalised C-chiral As–P ligands promoted by chiral cyclometallated complexes

หน่วยงาน Nanyang Technological University, Singapore

รายละเอียด

ชื่อเรื่อง : Asymmetric hydroarsination reactions toward synthesis of alcohol functionalised C-chiral As–P ligands promoted by chiral cyclometallated complexes
นักวิจัย : Cheow, Yuen Lin , Pullarkat, Sumod A. , Li, Yongxin , Leung, Pak-Hing
คำค้น : DRNTU::Science::Chemistry::Organic chemistry::Organometallic compounds.
หน่วยงาน : Nanyang Technological University, Singapore
ผู้ร่วมงาน : -
ปีพิมพ์ : 2555
อ้างอิง : 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. , 0022-328X , http://hdl.handle.net/10220/17145 , http://dx.doi.org/10.1016/j.jorganchem.2011.09.016
ที่มา : -
ความเชี่ยวชาญ : -
ความสัมพันธ์ : Journal of organometallic chemistry
ขอบเขตของเนื้อหา : -
บทคัดย่อ/คำอธิบาย :

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.

บรรณานุกรม :
Cheow, Yuen Lin , Pullarkat, Sumod A. , Li, Yongxin , Leung, Pak-Hing . (2555). Asymmetric hydroarsination reactions toward synthesis of alcohol functionalised C-chiral As–P ligands promoted by chiral cyclometallated complexes.
    กรุงเทพมหานคร : Nanyang Technological University, Singapore.
Cheow, Yuen Lin , Pullarkat, Sumod A. , Li, Yongxin , Leung, Pak-Hing . 2555. "Asymmetric hydroarsination reactions toward synthesis of alcohol functionalised C-chiral As–P ligands promoted by chiral cyclometallated complexes".
    กรุงเทพมหานคร : Nanyang Technological University, Singapore.
Cheow, Yuen Lin , Pullarkat, Sumod A. , Li, Yongxin , Leung, Pak-Hing . "Asymmetric hydroarsination reactions toward synthesis of alcohol functionalised C-chiral As–P ligands promoted by chiral cyclometallated complexes."
    กรุงเทพมหานคร : Nanyang Technological University, Singapore, 2555. Print.
Cheow, Yuen Lin , Pullarkat, Sumod A. , Li, Yongxin , Leung, Pak-Hing . Asymmetric hydroarsination reactions toward synthesis of alcohol functionalised C-chiral As–P ligands promoted by chiral cyclometallated complexes. กรุงเทพมหานคร : Nanyang Technological University, Singapore; 2555.