Preparation of homochiral phenolic crown ether having chiral subunits derived from (1R,2S)-cis-1,2,3,4-tetrahydronaphthalene-1,2$MI N@diol: temperature-dependent enantioselectivity in complexations with neutral amines

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Tetrahedron Asymmetry | / 15卷 / 2585期

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[1] Preparation of homochiral phenolic crown ether having chiral subunits derived from (1R,2S)-cis-1,2,3,4-tetrahydronaphthalene-1,2-diol: temperature-dependent enantioselectivity in complexations with neutral amines
Naemura, K
Wakebe, T
Hirose, K
Tobe, Y
TETRAHEDRON-ASYMMETRY, 1997, 8 (15) : 2585 - 2595
[2] Preparation of homochiral phenolic crown ethers containing para-substituted phenol moiety and chiral subunits derived from (S)-1-phenylethane-1,2-diol: Their chiral recognition behaviour in complexation with neutral amines
Naemura, K
Nishikawa, Y
Fuji, J
Hirose, K
Tobe, Y
TETRAHEDRON-ASYMMETRY, 1997, 8 (06) : 873 - 882
[3] Preparation of optically active azophenolic crown ethers containing 1-phenylethane-1,2-diol and 2,4-dimethyl-3-oxapentane-1,5-diol as a chiral subunit: temperature-dependent enantiomer selectivity in the complexation with chiral amines
Ogasahara, K
Hirose, K
Tobe, Y
Naemura, K
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1997, (21): : 3227 - 3236