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minfiensine

 
National Institutes of Health

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2018
2018
Olefin isomerization is a significant transformation in organic synthesis, which provides a convenient synthetic route for… Expand
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2017
2017
The first catalytic enantioselective asymmetric aza-pinacol rearrangement is reported. The reactions are catalyzed by a chiral… Expand
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2016
2016
The total synthesis of the Strychnos alkaloid (±)-minfiensine was achieved via an intramolecular amidofuran Diels-Alder… Expand
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2015
2015
An indoxyl-based strategy for the synthesis of indolines and indolenines via unprecedented aza-pinacol and aza-semipinacol… Expand
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2015
2015
This thesis describes a unified strategy for the synthesis of monoterpene indole alkaloids of the Aspidosperma family. These… Expand
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2011
2011
Eight new monoterpenoid indole alkaloids, gardfloramine-9-O-β-D-glucopyranoside (1), 19(E)-18-demethoxygardfloramine-N(4)-oxide… Expand
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Highly Cited
2011
Highly Cited
2011
Indoline alkaloids constitute a large class of natural products; their diverse and complex structures contribute to potent… Expand
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Highly Cited
2010
Highly Cited
2010
Two highly stereoselective cationic gold(I)-catalyzed tandem cyclization reactions of alkynylindoles are described. These… Expand
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Highly Cited
2008
Highly Cited
2008
A 1,2,3,4-tetrahydro-9a,4a-(iminoethano)-9H-carbazole (4) is a central structural feature of the Strychnos alkaloid minfiensine… Expand
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Highly Cited
2005
Highly Cited
2005
A catalytic asymmetric method for the chemical synthesis of alkaloids containing the 1,2,3,4-tetrahydro-9a,4a-(iminoethano)-9H… Expand
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