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Ent-Kaurane-based regio- and stereoselective inverse electron demand hetero-Diels-Alder reactions: Synthesis of dihydropyran-fused diterpenoids
Chunyong Ding
, Lili Wang
, Haijun Chen
, Christopher Wild
, Na Ye
, Ye Ding
, Tianzhi Wang
,
Mark A. White
, Qiang Shen
,
Jia Zhou
Biochemistry & Molecular Biology
Pharmacology & Toxicology
Research output
:
Contribution to journal
›
Article
›
peer-review
44
Scopus citations
Overview
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Dive into the research topics of 'Ent-Kaurane-based regio- and stereoselective inverse electron demand hetero-Diels-Alder reactions: Synthesis of dihydropyran-fused diterpenoids'. Together they form a unique fingerprint.
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Keyphrases
Dimerization
100%
Enones
100%
Regio
100%
Regioselectivity
100%
A-ring
100%
Stereoselectivity
100%
Diterpenoids
100%
Dihydropyran
100%
Ent-kaurane
100%
Reaction Synthesis
100%
Inverse Electron Demand
100%
Hetero-Diels-Alder Reaction
100%
Natural Products
50%
Oridonin
50%
Chemoresistance
50%
Ent-kaurane Diterpenoids
50%
Vinyl Sulfides
50%
Vinyl Ether
50%
Pyran Ring
50%
Cycloaddition
50%
Novel Anticancer Agent
50%
3,4-Dihydropyran
50%
Chemistry
Enone
100%
Diterpenoid
100%
Ent-Kaurane
100%
Hetero Diels-Alder Cycloaddition
100%
Dimerization
100%
Synthesis Reaction
100%
Ent-Kaurane Diterpenoid
50%
Vinyl Ether
50%
2H-Pyran Ring
50%
Natural Product
50%
Cycloaddition
50%