(R)-N-(1-naphthalen-1-ylethyl)-p,p-diphenylphosphinc amide

Base Information

Chemical Name:(R)-N-(1-naphthalen-1-ylethyl)-p,p-diphenylphosphinc amide
CAS No.:23943-58-0
Molecular Formula:C₂₄H₂₂NOP
Molecular Weight:371.419
Hs Code.:

Synonyms:(R)-N-(1-naphthalen-1-ylethyl)-p,p-diphenylphosphinc amide

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Chemical Property of (R)-N-(1-naphthalen-1-ylethyl)-p,p-diphenylphosphinc amide

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Technology Process of (R)-N-(1-naphthalen-1-ylethyl)-p,p-diphenylphosphinc amide

There total 7 articles about (R)-N-(1-naphthalen-1-ylethyl)-p,p-diphenylphosphinc amide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 80.0%

: 942066-01-5
N-[(E)-1-(1-naphthyl)ethylidene]diphenylphosphinic amide

: 23943-58-0
(R)-N-(1-naphthalen-1-ylethyl)-p,p-diphenylphosphinc amide

Guidance literature:: With trimethylaluminum; (S)-[1,1']-binaphthalenyl-2,2'-diol; isopropyl alcohol; In toluene; at 60 ℃; for 20h;
DOI:10.1021/ol060110w

Reference yield:

: 82572-09-6
C₂₄H₂₀NOP

: 23943-58-0
(R)-N-(1-naphthalen-1-ylethyl)-p,p-diphenylphosphinc amide

Guidance literature:: With (Fe(CO)(Ph₂PCH=CHN-((S,S)-CH(Ph)CH(Ph))-NCH=CHPPh₂)); potassium tert-butylate; In isopropyl alcohol; at 30 ℃; for 1h; enantioselective reaction; Inert atmosphere; Glovebox;
DOI:10.1021/ol302079q

Reference yield:

: 82572-09-6
C₂₄H₂₀NOP

: 82598-06-9
(S)-(+)-N-<1-(1-Naphthyl)-ethyl>-diphenylphosphinamide

: 23943-58-0
(R)-N-(1-naphthalen-1-ylethyl)-p,p-diphenylphosphinc amide

Guidance literature:: With potassium 9-O-(1,2:5,6-di-O-isopropylidene-α-D-glucofuranosyl)-9-boratabicyclo<3.3.1>nonane; In tetrahydrofuran; at -100 ℃; for 0.5h; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
DOI:10.1021/jo00380a047