Diels−Alder Reaction−Aromatization Approach toward Functionalized Ring C Allocolchicinoids. Enantioselective Total Synthesis of (−)-7S-Allocolchicine

Andrei V. Vorogushin; Alexander V. Predeus; William D. Wulff; Hans-Jürgen Hansen

doi:10.1021/jo034420t

Diels−Alder Reaction−Aromatization Approach toward Functionalized Ring C Allocolchicinoids. Enantioselective Total Synthesis of (−)-7S-Allocolchicine

The Journal of Organic Chemistry ◽

10.1021/jo034420t ◽

2003 ◽

Vol 68 (15) ◽

pp. 5826-5831 ◽

Cited By ~ 46

Author(s):

Andrei V. Vorogushin ◽

Alexander V. Predeus ◽

William D. Wulff ◽

Hans-Jürgen Hansen

Keyword(s):

Total Synthesis ◽

Alder Reaction ◽

Diels Alder ◽

Enantioselective Total Synthesis ◽

Diels Alder Reaction

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ChemInform Abstract: Enantioselective Total Synthesis of (-)-Chlorothricolide via the Tandem Inter- and Intramolecular Diels-Alder Reaction of a Hexaenoate Intermediate.

ChemInform ◽

10.1002/chin.199849291 ◽

2010 ◽

Vol 29 (49) ◽

pp. no-no

Author(s):

W. R. ROUSH ◽

R. J. SCIOTTI

Keyword(s):

Total Synthesis ◽

Alder Reaction ◽

Diels Alder ◽

Enantioselective Total Synthesis ◽

Diels Alder Reaction

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Inside Back Cover: Bicyclic Guanidine Catalyzed Asymmetric Tandem Isomerization Intramolecular-Diels-Alder Reaction: The First Catalytic Enantioselective Total Synthesis of (+)-alpha-Yohimbine (Chem. Asian J. 3/2016)

Chemistry - An Asian Journal ◽

10.1002/asia.201600048 ◽

2016 ◽

Vol 11 (3) ◽

pp. 417-417

Author(s):

Wei Feng ◽

Danfeng Jiang ◽

Choon-Wee Kee ◽

Hongjun Liu ◽

Choon-Hong Tan

Keyword(s):

Total Synthesis ◽

Alder Reaction ◽

Diels Alder ◽

Back Cover ◽

Enantioselective Total Synthesis ◽

Diels Alder Reaction

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ChemInform Abstract: Enantioselective Total Synthesis of Glyoxalase I Inhibitor (I) Using Asymmetric Diels-Alder Reaction of a New Chiral Dienophile, (S)S-3-(3Trifluoromethylpyrid-2-ylsulfinyl)acrylate.

ChemInform ◽

10.1002/chin.198715370 ◽

1987 ◽

Vol 18 (15) ◽

Author(s):

H. TAKAYAMA ◽

K. HAYASHI ◽

T. KOIZUMI

Keyword(s):

Total Synthesis ◽

Alder Reaction ◽

Diels Alder ◽

Glyoxalase I ◽

Enantioselective Total Synthesis ◽

Diels Alder Reaction

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Intra- and intermolecular hetero-Diels-Alder reactions. 34. Enantioselective total synthesis of the mycotoxin (-)-talaromycin B by a hetero Diels-Alder reaction

The Journal of Organic Chemistry ◽

10.1021/jo00007a040 ◽

1991 ◽

Vol 56 (7) ◽

pp. 2476-2481 ◽

Cited By ~ 38

Author(s):

Lutz F. Tietze ◽

Christoph Schneider

Keyword(s):

Total Synthesis ◽

Alder Reaction ◽

Diels Alder ◽

Enantioselective Total Synthesis ◽

Diels Alder Reaction

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Bicyclic Guanidine Catalyzed Asymmetric Tandem Isomerization Intramolecular-Diels-Alder Reaction: The First Catalytic Enantioselective Total Synthesis of (+)-alpha-Yohimbine

Chemistry - An Asian Journal ◽

10.1002/asia.201500246 ◽

2015 ◽

Vol 11 (3) ◽

pp. 390-394 ◽

Cited By ~ 8

Author(s):

Wei Feng ◽

Danfeng Jiang ◽

Choon-Wee Kee ◽

Hongjun Liu ◽

Choon-Hong Tan

Keyword(s):

Total Synthesis ◽

Alder Reaction ◽

Diels Alder ◽

Enantioselective Total Synthesis ◽

Diels Alder Reaction

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ChemInform Abstract: Enantioselective Total Synthesis of (-)-Equisetin Using a Me3Al-Mediated Intramolecular Diels-Alder Reaction.

ChemInform ◽

10.1002/chin.200126225 ◽

2010 ◽

Vol 32 (26) ◽

pp. no-no

Author(s):

Kumiko Yuki ◽

Mitsuru Shindo ◽

Kozo Shishido

Keyword(s):

Total Synthesis ◽

Alder Reaction ◽

Diels Alder ◽

Enantioselective Total Synthesis ◽

Diels Alder Reaction

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Enantioselective total synthesis of Glyoxalase I inhibitor using asymmetric Diels-Alder reaction of a new chiral dienophile, ()S-3-(3-triflouromethylpyrid-2-ylsulfinyl)acrylate.

Tetrahedron Letters ◽

10.1016/s0040-4039(00)85252-1 ◽

1986 ◽

Vol 27 (45) ◽

pp. 5509-5512 ◽

Cited By ~ 48

Author(s):

Hiromitsu Takayama ◽

Kazuya Hayashi ◽

Toru Koizumi

Keyword(s):

Total Synthesis ◽

Alder Reaction ◽

Diels Alder ◽

Glyoxalase I ◽

Enantioselective Total Synthesis ◽

Diels Alder Reaction

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Enantioselective Total Synthesis of (+)-6-epi-Mevinolin and Its Analogs. Efficient Construction of the Hexahydronaphthalene Moiety by High Pressure-Promoted Intramolecular Diels−Alder Reaction of (R,2Z,8E,10E)-1-[(tert-Butyldimethylsilyl)oxy]-6-methyl-2,8,10-dodecatrien-4-one

The Journal of Organic Chemistry ◽

10.1021/jo970444m ◽

1997 ◽

Vol 62 (16) ◽

pp. 5299-5309 ◽

Cited By ~ 23

Author(s):

Yoshitaka Araki ◽

Toshiro Konoike

Keyword(s):

High Pressure ◽

Total Synthesis ◽

Alder Reaction ◽

Diels Alder ◽

Enantioselective Total Synthesis ◽

Diels Alder Reaction ◽

Efficient Construction

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ChemInform Abstract: Regiocontrol by Remote Substituents. An Enantioselective Total Synthesis of Frenolicin B via a Highly Regioselective Diels-Alder Reaction.

ChemInform ◽

10.1002/chin.199345299 ◽

2010 ◽

Vol 24 (45) ◽

pp. no-no

Author(s):

G. A. KRAUS ◽

J. LI ◽

M. S. GORDON ◽

J. H. JENSEN

Keyword(s):

Total Synthesis ◽

Alder Reaction ◽

Diels Alder ◽

Enantioselective Total Synthesis ◽

Diels Alder Reaction

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ChemInform Abstract: Intra- and Intermolecular Hetero-Diels-Alder Reactions. Part 34. Enantioselective Total Synthesis of the Mycotoxim (-)-Talaromycin B (I) by a Hetero-Diels-Alder Reaction.

ChemInform ◽

10.1002/chin.199135283 ◽

2010 ◽

Vol 22 (35) ◽

pp. no-no

Author(s):

L. F. TIETZE ◽

C. SCHNEIDER

Keyword(s):

Total Synthesis ◽

Alder Reaction ◽

Diels Alder ◽

Enantioselective Total Synthesis ◽

Diels Alder Reaction

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