Diamidophosphites from β-hydroxyamides: readily assembled ligands for Pd-catalyzed asymmetric allylic substitution. Issue 17 (14th April 2020)
- Record Type:
- Journal Article
- Title:
- Diamidophosphites from β-hydroxyamides: readily assembled ligands for Pd-catalyzed asymmetric allylic substitution. Issue 17 (14th April 2020)
- Main Title:
- Diamidophosphites from β-hydroxyamides: readily assembled ligands for Pd-catalyzed asymmetric allylic substitution
- Authors:
- Chuchelkin, Ilya V.
Gavrilov, Konstantin N.
Borisova, Nataliya E.
Perepukhov, Alexander M.
Maximychev, Alexander V.
Zheglov, Sergey V.
Gavrilov, Vladislav K.
Firsin, Ilya D.
Zimarev, Vladislav S.
Mikhel, Igor S.
Tafeenko, Victor A.
Murashova, Elena V.
Chernyshev, Vladimir V.
Goulioukina, Nataliya S. - Abstract:
- Abstract : Novel diamidophosphites based on β-hydroxyamides were prepared, and their individual and in situ formed complexes were tested in Pd-mediated allylations. Abstract : Two groups of modular chiral diamidophosphite ligands were easily synthesised from accessible N -Boc-amino alcohols and pseudodipeptides. The reaction of these compounds with [Pd(allyl)Cl]2 in the presence of AgBF4 yielded complexes [Pd(allyl)(L)2 ]BF4 . In addition, metallochelates [Pd(allyl)(L)]BF4 with ( S )-methioninol-based P, S -bidentate ligands were prepared. The structures of the novel ligands and complexes were elucidated by means of 2D-NMR and were confirmed by single-crystal X-ray diffraction, as well as by DFT calculations. Asymmetric inducers of this type exhibited high enantioselectivities in the Pd-mediated allylic substitution of ( E )-1, 3-diphenylallyl ethyl carbonate with CH2 (CO2 Me)2 (up to 98% ee) and (CH2 )4 NH (up to 92% ee). Ee values of up to 86% and 73% were obtained in the Pd-catalyzed allylic alkylation of cinnamyl acetate with ethyl 2-oxocyclohexane-1-carboxylate and ethyl 2-oxocyclopentane-1-carboxylate, respectively. The effects of the structural modules, such as the nature of the phosphorus-containing ring or exocyclic substituent, on the catalytic activity and enantioselectivity were investigated.
- Is Part Of:
- Dalton transactions. Volume 49:Issue 17(2020)
- Journal:
- Dalton transactions
- Issue:
- Volume 49:Issue 17(2020)
- Issue Display:
- Volume 49, Issue 17 (2020)
- Year:
- 2020
- Volume:
- 49
- Issue:
- 17
- Issue Sort Value:
- 2020-0049-0017-0000
- Page Start:
- 5625
- Page End:
- 5635
- Publication Date:
- 2020-04-14
- Subjects:
- Chemistry, Inorganic -- Periodicals
Chemistry, Physical and theoretical -- Periodicals
Chemistry, Inorganic -- Periodicals
546.05 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/dt#!issueid=dt043040&type=current&issnprint=1477-9226 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d0dt00741b ↗
- Languages:
- English
- ISSNs:
- 1477-9226
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3517.830000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 13857.xml