Asymmetric syntheses of diarylheptanoid natural products (−)-centrolobine and (−)-de- O-methylcentrolobine via hetero-Diels–Alder reaction catalyzed by dirhodium(II) tetrakis[( R)-3-(benzene-fused-phthalimido)-2-piperidinonate]
Catalytic asymmetric syntheses of (−)-centrolobine and (−)-de- O-methylcentrolobine have been achieved, incorporating a hetero-Diels–Alder (HDA) reaction between 4-aryl-2-silyloxy-1,3-butadienes and phenylpropargyl aldehyde derivatives as a key step. The HDA reaction using dirhodium(II) tetrakis[( R...
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Published in | Tetrahedron Vol. 63; no. 48; pp. 12037 - 12046 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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26.11.2007
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Abstract | Catalytic asymmetric syntheses of (−)-centrolobine and (−)-de-
O-methylcentrolobine have been achieved, incorporating a hetero-Diels–Alder (HDA) reaction between 4-aryl-2-silyloxy-1,3-butadienes and phenylpropargyl aldehyde derivatives as a key step. The HDA reaction using dirhodium(II) tetrakis[(
R)-3-(benzene-fused-phthalimido)-2-piperidinonate], Rh
2(
R-BPTPI)
4, as a chiral Lewis acid catalyst provides exclusively
cis-2,6-disubstituted tetrahydropyran-4-ones in up to 93% ee.
[Display omitted] |
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AbstractList | Catalytic asymmetric syntheses of (−)-centrolobine and (−)-de-
O-methylcentrolobine have been achieved, incorporating a hetero-Diels–Alder (HDA) reaction between 4-aryl-2-silyloxy-1,3-butadienes and phenylpropargyl aldehyde derivatives as a key step. The HDA reaction using dirhodium(II) tetrakis[(
R)-3-(benzene-fused-phthalimido)-2-piperidinonate], Rh
2(
R-BPTPI)
4, as a chiral Lewis acid catalyst provides exclusively
cis-2,6-disubstituted tetrahydropyran-4-ones in up to 93% ee.
[Display omitted] Catalytic asymmetric syntheses of (-)-centrolobine and (-)-de-O-methylcentrolobine have been achieved, incorporating a hetero-Diels-Alder (HDA) reaction between 4-aryl-2-silyloxy-1,3-butadienes and phenylpropargyl aldehyde derivatives as a key step. The HDA reaction using dirhodium(II) tetrakis[(R)-3-(benzene-fused-phthalimido)-2-piperidinonate], Rh-2(R-BPTPI)(4), as a chiral Lewis acid catalyst provides exclusively cis-2,6-disubstituted tetrahydropyran-4-ones in up to 93% ee. (C) 2007 Elsevier Ltd. All rights reserved. |
Author | Hashimoto, Shunichi Anada, Masahiro Washio, Takuya Yamaguchi, Reika Abe, Takumi Nambu, Hisanori |
Author_xml | – sequence: 1 givenname: Takuya surname: Washio fullname: Washio, Takuya – sequence: 2 givenname: Reika surname: Yamaguchi fullname: Yamaguchi, Reika – sequence: 3 givenname: Takumi surname: Abe fullname: Abe, Takumi – sequence: 4 givenname: Hisanori surname: Nambu fullname: Nambu, Hisanori – sequence: 5 givenname: Masahiro surname: Anada fullname: Anada, Masahiro – sequence: 6 givenname: Shunichi surname: Hashimoto fullname: Hashimoto, Shunichi email: hsmt@pharm.hokudai.ac.jp |
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Keywords | Hetero-Diels–Alder reaction Chiral Rh(II) catalyst (−)-De- O-methylcentrolobine Diarylheptanoids (−)-Centrolobine diarylheptanoids chiral Rh(II) catalyst CARBONYL-COMPOUNDS DIOSPONGIN-A (-)-de-O-methylcentrolobine ANTIPROLIFERATIVE DIARYLHEPTANOIDS (-)-centrolobine BIOLOGICAL EVALUATION BLEPHAROCALYXINS C-E STEREOSELECTIVE-SYNTHESIS PRINS CYCLIZATIONS ENANTIOSELECTIVE TOTAL-SYNTHESIS ALPINIA-BLEPHAROCALYX EPICALYXIN-F hetero-Diels-Alder reaction |
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Snippet | Catalytic asymmetric syntheses of (−)-centrolobine and (−)-de-
O-methylcentrolobine have been achieved, incorporating a hetero-Diels–Alder (HDA) reaction... Catalytic asymmetric syntheses of (-)-centrolobine and (-)-de-O-methylcentrolobine have been achieved, incorporating a hetero-Diels-Alder (HDA) reaction... |
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SubjectTerms | (−)-Centrolobine (−)-De- O-methylcentrolobine Chemistry Chemistry, Organic Chiral Rh(II) catalyst Diarylheptanoids Hetero-Diels–Alder reaction Physical Sciences Science & Technology |
Title | Asymmetric syntheses of diarylheptanoid natural products (−)-centrolobine and (−)-de- O-methylcentrolobine via hetero-Diels–Alder reaction catalyzed by dirhodium(II) tetrakis[( R)-3-(benzene-fused-phthalimido)-2-piperidinonate] |
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