Paul Wyatt

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Name:
Organization: University of Bristol , England
Department: School of Chemistry
Title: Teaching Fellow(PhD)
Co-reporter:Paul Wyatt;Helen Eley;Jonathan Charmant;Berian J. Daniel;Anob Kantacha
European Journal of Organic Chemistry 2003 Volume 2003(Issue 21) pp:
Publication Date(Web):16 OCT 2003
DOI:10.1002/ejoc.200300396

An asymmetric synthesis of C3-symmetric phosphane 1 has been achieved. Two of the α-methylbenzyl groups were introduced as nucleophiles (using an α-methylbenzyl Grignard reagent), and asymmetry was introduced by resolution using (R)-α-methylbenzylamine. The final α-methylbenzyl group was introduced as an electrophile (α-methylbenzyl iodide) in a modestly selective reaction. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)

Phosphinic amide, N-[(1R)-1-phenylethyl]-P,P-bis[(1S)-1-phenylethyl]-
Phosphine oxide, bis[(1R)-1-phenylethyl][(1S)-1-phenylethyl]-, rel-
Phosphinic chloride, bis[(1S)-1-phenylethyl]-
Phosphinic acid, bis[(1S)-1-phenylethyl]-
PHOSPHINIC AMIDE, P-[(1S)-1-PHENYLETHYL]-N,P-BIS[(1R)-1-PHENYLETHYL]-
MAGNESIUM, CHLORO(1-PHENYLETHYL)-
PHOSPHINE, TRIS[(1S)-1-PHENYLETHYL]-
PHOSPHINIC AMIDE, N,P,P-TRIS[(1R)-1-PHENYLETHYL]-
1,2-ETHANEDIOL, 1,2-BIS(3-FLUOROPHENYL)-, (1S,2S)-
1,2-Ethanediol, 1,2-bis(3-fluorophenyl)-, (1R,2R)-rel-