Convergent Strategies in Total Syntheses of Complex Terpenoids.
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Navigating the Chiral Pool in the Total Synthesis of Complex Terpene Natural Products.A total synthesis of (-)-Hortonone C.Schinortriterpenoids: A Case Study in Synthetic Design.The synthesis of cardenolide and bufadienolide aglycones, and related steroids bearing a heterocyclic subunit.Modular Terpenoid Construction via Catalytic Enantioselective Formation of All-Carbon Quaternary Centers: Total Synthesis of Oridamycin A, Triptoquinones B and C, and Isoiresin.Total synthesis of avenaol.Selective Synthesis of Cyclooctanoids by Radical Cyclization of Seven-Membered Lactones: Neutron Diffraction Study of the Stereoselective Deuteration of a Chiral Organosamarium Intermediate.Multicomponent Double Diels-Alder/Nazarov Tandem Cyclization of Symmetric Cross-Conjugated Diynones to Generate [6-5-6] Tricyclic Products.Specialized Plant Metabolism Characteristics and Impact on Target Molecule Biotechnological Production.An Enyne Cope Rearrangement Enables Polycycloalkane Synthesis from Readily Available Starting Materials.Direct assembly of multiply oxygenated carbon chains by decarbonylative radical-radical coupling reactions.A Concise Route to the Strongylophorines.Regiodivergent Remote Arylation of Cycloalkanols to Dysideanone's Fused Carbotetracycles and Its Bridged Isomers.Wolff/Cope Approach to the AB Ring of the Sesterterpenoid Variecolin.Total Syntheses of Sesterterpenoid Ansellones A and B, and Phorbadione.A three-component coupling approach to the ACE-ring substructure of C19-diterpene alkaloids.Expedient and Diastereodivergent Assembly of Terpenoid Decalin Subunits having Quaternary Stereocenters through Organocatalytic Robinson Annulation of Nazarov Reagent.Bioinspired synthesis of pentacyclic onocerane triterpenoids.Unified Total Synthesis of 3-epi-Ryanodol, Cinnzeylanol, Cinncassiols A and B, and Structural Revision of Natural Ryanodol and Cinnacasol.Modular access to functionalized 5–8–5 fused ring systems via a photoinduced cycloisomerization reaction† †Electronic supplementary information (ESI) available: Experimental procedures at characterization data. CCDC 1816383–1816390. For ESI and crys
P2860
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P2860
Convergent Strategies in Total Syntheses of Complex Terpenoids.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Convergent Strategies in Total Syntheses of Complex Terpenoids.
@en
type
label
Convergent Strategies in Total Syntheses of Complex Terpenoids.
@en
prefLabel
Convergent Strategies in Total Syntheses of Complex Terpenoids.
@en
P2093
P356
P1433
P1476
Convergent Strategies in Total Syntheses of Complex Terpenoids.
@en
P2093
Daisuke Urabe
Masayuki Inoue
Taro Asaba
P304
P356
10.1021/CR500716F
P577
2015-03-17T00:00:00Z