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 inTetrahedron Vol. 63; no. 48; pp. 12037 - 12046
Main Authors Washio, Takuya, Yamaguchi, Reika, Abe, Takumi, Nambu, Hisanori, Anada, Masahiro, Hashimoto, Shunichi
Format Journal Article
LanguageEnglish
Published OXFORD Elsevier Ltd 26.11.2007
Elsevier
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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]
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
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  email: hsmt@pharm.hokudai.ac.jp
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Issue 48
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]
URI https://dx.doi.org/10.1016/j.tet.2007.09.003
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