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Tetrahedron Letters

Volumn 32, Issue 38, 1991, Pages 5089-5092

Preparation of optically pure 1,2,5-triphenylphospholane. Use as ligand for enantioselective transition-metal catalysis.

(2) Fiaud, Jean Claude a Legros, Jean Yves a

a CNRS (France)

Author keywords

Base catalyzed isomerization Chiral Chromatography; Chiral phosphine oxides; Chiral phosphines; Palladium catalyzed allylic substitution

Indexed keywords

1,2,5 TRIPHENYLPHOSPHOLANE OXIDE; ORGANOPHOSPHORUS COMPOUND; UNCLASSIFIED DRUG;

ARTICLE; ENANTIOMER; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; SUPERCRITICAL FLUID CHROMATOGRAPHY;

EID: 0025884944 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(00)93435-X Document Type: Article

Times cited : (44)

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7
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14
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18
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- D = −150(c 1, MeOH) for the first-eluted enantiomer. X-Ray determination of the absolute configuration is presently under way.

19
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- Asymmetric catalytic reduction with transition metal complexes. I. Catalytic system of rhodium(I) with (-)-2,3-0-isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)butane, a new chiral diphosphine
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20
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- Morrison¹ Mosher²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.