The orientation of the β-hydroxyl group controls the diastereoselectivity during the hydride reduction and Grignard reaction of inososes

Tetrahedron

Volumn 69, Issue 25, 2013, Pages 5144-5151

  Jagdhane, Rajendra C ^a,b   Patil, Madhuri T ^a   Krishnaswamy, Shobhana ^a   Shashidhar, Mysore S ^a  

^a NATIONAL CHEMICAL LABORATORY   (India)

^b UNIVERSITY OF SASKATCHEWAN   (Canada)

Author keywords

Cyclitol; Diastereoselectivity; Grignard; Inositol; Nucleophile; Reduction

Indexed keywords

2 O METHYL EPI INOSITOL; ALCOHOL; BETA HYDROXYL GROUP; CARBONYL DERIVATIVE; CHEMICAL COMPOUND; EPI INOSOSE; HYDROXYL GROUP; INOSITOL DERIVATIVE; ISO LAMINITOL; ISO MYTILITOL; ONONITOL; SCYLLO INOSOSE; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; DIASTEREOSELECTIVITY; EPIMER; GRIGNARD REACTION; HYDRIDE REDUCTION; ISOMER; PRIORITY JOURNAL; REDUCTION; STEREOCHEMISTRY;

EID: 84877730082     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2013.04.081     Document Type: Article

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