913472
(2S,2S′,3S,3S′)-WingPhos
≥95%
Sinônimo(s):
(2S,2′S,3S,3′S)-4,4′-Di(anthracen-9-yl)-3,3′-di-tert-butyl-2,2′,3,3′-tetrahydro-2,2′-bibenzo[d][1,3]oxaphosphole
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About This Item
Fórmula empírica (Notação de Hill):
C50H44O2P2
Número CAS:
Peso molecular:
738.83
Código UNSPSC:
12352200
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Ensaio
≥95%
forma
powder or crystals
pureza óptica
ee: ≥99% (HPLC)
adequação da reação
reagent type: ligand
grupo funcional
phosphine
Aplicação
(2S,2S′,3S,3S′)-WingPhos is a P-chiral biphosphorus ligand for Rh-catalyzed asymmetric hydrogenations as well as Rh-catalyzed asymmetric addition of aryl boroxines to ketones.
Product can be used with our benchtop hydrogen generator, H-Genie Lite (Z744083)
Product can be used with our benchtop hydrogen generator, H-Genie Lite (Z744083)
Informações legais
Sold in collaboration with Zejun Pharmaceuticals
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Nº do produto
Descrição
Preços
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Certificados de análise (COA)
Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.
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Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.
Design of phosphorus ligands with deep chiral pockets: practical synthesis of chiral β-arylamines by asymmetric hydrogenation.
Guodu Liu et al.
Angewandte Chemie (International ed. in English), 52(15), 4235-4238 (2013-03-16)
Linwei Huang et al.
Angewandte Chemie (International ed. in English), 55(14), 4527-4531 (2016-03-05)
Highly enantioselective additions of arylboroxines to simple aryl ketones have been achieved for the first time with a Rh/(R,R,R,R)-WingPhos catalyst, thus providing a range of chiral diaryl alkyl carbinols with excellent ee values and yields. (R,R,R,R)-WingPhos has been proven to be
Jinbin Zhu et al.
Angewandte Chemie (International ed. in English), 58(45), 16119-16123 (2019-08-31)
Highly enantioselective rhodium-catalyzed addition of arylboroxines to N-unprotected ketimines is realized for the first time by employing chiral BIBOP-type ligands with a Rh loading as low as 1 mol %. A range of chiral α-trifluoromethyl-α,α-diaryl α-tertiary amines or 3-amino-3-aryloxindoles were formed with
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