| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1349842 | Tetrahedron: Asymmetry | 2009 | 4 Pages |
The direct and versatile stereoselective synthesis of a novel class of cyclopropyl derivatives of pyroglutamic acid is reported, using substituted diaryldiazo compounds. The course of the reaction has been investigated, and yields of substituted fluorenylcyclopropanes are greater than those of diphenylmethylcyclopropane analogues.
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7,7-Diphenyl-9-oxo-2-phenyl-1-aza-3-oxa-tricyclo[4.3.04, 5.06, 8]nonan-2-oneC25H21NO2[α]D = +78.3 (c 1, CHCl3)Source of chirality: (S)-pyroglutamic acidAbsolute configuration: (2R,5S,6S,7R)
7,8-Diaza-2-oxa-3,6a,6a-triphenyl-1,2,3,5a,6,8b-hexahydrocyclopenta[a]pyrrolizin-5(8aH)-oneC25H21N3O2[α]D = +565.5 (c 1, CHCl3)Source of chirality: (S)-pyroglutamic acidAbsolute configuration: (2R,5S,6S,7R)
6-benzhydryl-8-oxo-2-phenyl-1-aza-3-oxa-bicyclo[3.3.0]oct-6-eneC25H21NO2[α]D = +69.6 (c 1, CHCl3)Source of chirality: (S)-pyroglutamic acidAbsolute configuration: (2R,5S)
Spiro[9-oxo-2-phenyl-1-aza-3-oxa-tricyclo[4.3.04,5.06,8]nonan-2-one-7,9’-fluorene]C25H19NO2[α]D = +257.3 (c 6.2, CHCl3)Source of chirality: (S)-pyroglutamic acidAbsolute configuration: (2R,5S,6S,7R)
7,7-Di(p-iodophenyl)-8-ethoxycarbonyl-9-oxo-2-phenyl-1-aza-3-oxa-tricyclo[4.3.04, 5.06, 8]nonan-2-oneC28H23I2NO4[α]D = −30.2 (c 6.3, CHCl3)Source of chirality: (S)-pyroglutamic acidAbsolute configuration: (2R,5S,6R,7R)
7,7-Di(p-iodophenyl)-8-ethoxycarbonyl-9-oxo-2-phenyl-1-aza-3-oxa-tricyclo[4.3.04, 5.06, 8]nonan-2-oneC28H25NO4[α]D = +235.6 (c 3, CHCl3)Source of chirality: (S)-pyroglutamic acidAbsolute configuration: (2R,5S,6R,7R)
7,7-Diphenyl-8-ethoxycarbonyl-9-oxo-2-phenyl-1-aza-3-oxa-tricyclo[4.3.04, 5.06, 8]nonan-2-oneC30H29NO6[α]D = −69.7 (c 1, CHCl3)Source of chirality: (S)-pyroglutamic acidAbsolute configuration: (2R,5S,6R,7R)
6-Benzhydryl-7-ethoxycarbonyl-8-oxo-2-phenyl-1-aza-3-oxa-bicyclo[3.3.0]oct-6-eneC28H25NO4[α]D = +195.3 (c 1, CHCl3)Source of chirality: (S)-pyroglutamic acidAbsolute configuration: (2R,5S)
6-(Dimethoxy)benzhydryl-7-ethoxycarbonyl-8-oxo-2-phenyl-1-aza-3-oxabicyclo[3.3.0]oct-6-eneC23H22NO5[α]D = +31.7 (c 2.2, CHCl3)Source of chirality: (S)-pyroglutamic acidAbsolute configuration: (2R,5S)
Spiro[8-ethoxycarbonyl-9-oxo-2-phenyl-1-aza-3-oxa-tricyclo[4.3.04,5.06,8]nonan-2-one-7,9’-fluorene]C28H23NO4[α]D = +145.5 (c 2.4, CHCl3)Source of chirality: (S)-pyroglutamic acidAbsolute configuration: (2R,5S,6R,7R)
4’-Hydroxymethylspiro[8-ethoxycarbonyl-9-oxo-2-phenyl-1-aza-3-oxa-tricyclo[4.3.04,5.06,8]nonan-2-one-7,9’-fluorene]C29H25NO5[α]D = +131.0 (c 1, CHCl3)Source of chirality: (S)-pyroglutamic acidAbsolute configuration: (2R,5S,6R,7R,9S)
4’-Hydroxymethylspiro[8-ethoxycarbonyl-9-oxo-2-phenyl-1-aza-3-oxa-tricyclo[4.3.04,5.06,8]nonan-2-one-7,9’-fluorene]C29H25NO5[α]D = +133 (c 1, CHCl3)Source of chirality: (S)-pyroglutamic acidAbsolute configuration: (2R,5S,6R,7R,9R)
3’-Bromospiro[8-ethoxycarbonyl-9-oxo-2-phenyl-1-aza-3-oxa-tricyclo[4.3.04,5.06,8]nonan-2-one-7,9’-fluorene]C28H22BrNO4[α]D = +156.9 (c 0.8, CHCl3)Source of chirality: (S)-pyroglutamic acidAbsolute configuration: (2R,5S,6R,7R,9S)
3’-Bromospiro[8-ethoxycarbonyl-9-oxo-2-phenyl-1-aza-3-oxa-tricyclo[4.3.04,5.06,8]nonan-2-one-7,9’-fluorene]C28H22BrNO4[α]D = +42.2 (c 1, CHCl3)Source of chirality: (S)-pyroglutamic acidAbsolute configuration: (2R,5S,6R,7R,9R)
Spiro[8-ethoxycarbonyl-9-oxo-2-phenyl-1-aza-3-oxa-tricyclo[4.3.04,5.06,8]nonan-2-one-7,5’-indeno[1,2-b]pyridine]C28H21Br2NO4[α]D = +69.1 (c 0.75, CHCl3)Source of chirality: (S)-pyroglutamic acidAbsolute configuration: (2R,5S,6R,7R)
3′-Dibromospiro[8-ethoxycarbonyl-9-oxo-2-phenyl-1-aza-3-oxa-tricyclo[4.3.04,5.06,8]nonan-2-one-7,9’-fluorene]C27H22N2O4[α]D = +96.4 (c 1, CHCl3)Source of chirality: (S)-pyroglutamic acidAbsolute configuration: (2R,5S,6R,7R,9S)
Spiro[8-ethoxycarbonyl-9-oxo-2-phenyl-1-aza-3-oxa-tricyclo[4.3.04,5.06,8]nonan-2-one-7,5’-indeno[1,2-b]pyridine]C27H22N2O4[α]D = +111 (c 1, CHCl3)Source of chirality: (S)-pyroglutamic acidAbsolute configuration: (2R,5S,6R,7R,9R)
4’,5’-Diazaspiro[9-oxo-2-phenyl-1-aza-3-oxa-tricyclo[4.3.04,5.06,8]nonan-2-one-7,9’-fluorene]C26H21N3O4[α]D = +77.9 (c 1.7, CHCl3)Source of chirality: (S)-pyroglutamic acidAbsolute configuration: (2R,5S,6R,7R)
6’,7’-Diaza-5a,8-diethoxycarbonyl-2-oxa-3-phenyl-1,2,3,5a,6,8b-hexahydrocyclopenta[a]pyrrolizin-5(8aH)-oneC19H21N3O6[α]D = −52.2 (c 4.6, CHCl3)Source of chirality: (S)-pyroglutamic acidAbsolute configuration: (2R,5S,6R,7R)
