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Volumn 17, Issue 8, 2006, Pages 1189-1198

Corrigendum to "Studies on epoxidation of enantiomerically pure 2,3-dideoxy hex-2-enitols: a convenient access to highly functionalized enantiomerically pure tetrahydrofuran derivatives". [Tetrahedron: Asymmetry 17 (2006) 1189] (DOI:10.1016/j.tetasy.2006.04.022);Studies on epoxidation of enantiomerically pure 2,3-dideoxy hex-2-enitols: a convenient access to highly functionalized enantiomerically pure tetrahydrofuran derivatives

Author keywords

[No Author keywords available]

Indexed keywords

2,3 DIDEOXY HEX 2 ENITOL DERIVATIVE; 2,3 EPOXY ALCOHOL; 3 CHLOROPERBENZOIC ACID; 4,5,6 TRI O ACETYL 2,3 EPOXY GALACTITOL; 4,5,6 TRI O ACETYL 2,3 EPOXY GLUCITOL; 4,5,6 TRI O BENZYL 2,3 EPOXY GALACTITOL; 4,5,6 TRI O BENZYL 2,3 EPOXY GLUCITOL; 4,6 DI O BENZYL 2,3 EPOXY GALACTITOL; 4,6 DI O BENZYL 2,3 EPOXY GLUCITOL; 4,6 DI O BENZYL 5 O ACETYL 2,3 EPOXY GALACTITOL; ALCOHOL; REAGENT; TETRAHYDROFURAN DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33646841651     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2006.06.035     Document Type: Erratum
Times cited : (20)

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    • note
    • 1H NMR spectra of the diacetate derivative of the mixture of 15 or 17.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.