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Volumn 62, Issue 49, 2006, Pages 11402-11412

Enantioselective homoallyl-cyclopropanation of dibenzylideneacetone by modified allylindium halide reagents-rapid access to enantioenriched 1-styryl-norcarene

Author keywords

[No Author keywords available]

Indexed keywords

ACETONE; ALDEHYDE; ALLYL COMPOUND; AMINOALCOHOL; CARBON; CINCHONA ALKALOID; CYCLOPROPANE; CYCLOPROPANE DERIVATIVE; DIBENZYLIDENEACETONE; EPHEDRA EXTRACT; HALIDE; INDIUM; IODINE; IODINE DERIVATIVE; KETONE DERIVATIVE; LIGAND; MANDELIC ACID; MANDELIC ACID DERIVATIVE; OXYGEN; REAGENT; SODIUM SULFATE; TARTARIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33751068779     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.05.003     Document Type: Article
Times cited : (22)

References (125)
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    • Allyl indium halide reagents (generated from allyl iodide or bromide, using In metal or In(I)I) are reported to add exclusively [1,2]- to enones and enals, see Ref. 7a,b.
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    • 4) without racemisation, see Section 4 for details.
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    • note
    • It should be noted that in the homoallyl-cyclopropanation reaction the acidic surface of the silica gel plate can induce cyclopropane formation and that TLC analysis must thus be interpreted with caution.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.