Modern synthetic efforts toward biologically active terpenes.
about
Scalable enantioselective total synthesis of taxanesCombating pathogenic microorganisms using plant-derived antimicrobials: a minireview of the mechanistic basisThe first structure of a bacterial diterpene cyclase: CotB2Natural terpenoids from Ambrosia species are active in vitro and in vivo against human pathogenic trypanosomatidsNatural products as chemical probesA 15-step synthesis of (+)-ryanodol.Catalyst-controlled formal [4 + 3] cycloaddition applied to the total synthesis of (+)-barekoxide and (-)-barekol.Mechanism, reactivity, and selectivity of nickel-catalyzed [4 + 4 + 2] cycloadditions of dienes and alkynes.De novo branching cascades for structural and functional diversity in small molecules.Gold(I)-Catalyzed Desymmetrization of 1,4-Dienes by an Enantioselective Tandem Alkoxylation/Claisen Rearrangement.Enantioselective synthesis of an ophiobolin sesterterpene via a programmed radical cascadeChemical synthesis of the englerins.Phytol-derived novel isoprenoid immunostimulants.Synthetic approaches toward sesterterpenoids.Bioprospecting of marine invertebrates for new natural products - a chemical and zoogeographical perspective.Biogeography and biodiscovery hotspots of macroalgal marine natural products.The isolation and synthesis of neodolastane diterpenoids.Chemistry and Biology of Resveratrol-Derived Natural ProductsTerpenoid-Alkaloids: Their Biosynthetic Twist of Fate and Total SynthesisNavigating the Chiral Pool in the Total Synthesis of Complex Terpene Natural Products.Mechanistic studies of sesquiterpene cyclases based on their carbon isotope ratios at natural abundance.A total synthesis of (-)-Hortonone C.Analysis of terpenes and turpentines using gas chromatography with vacuum ultraviolet detection.Scalable, enantioselective synthesis of germacrenes and related sesquiterpenes inspired by terpene cyclase phase logicSynthesis at the molecular frontier.An approach to mimicking the sesquiterpene cyclase phase by nickel-promoted diene/alkyne cooligomerizationAtropurpuran - Missing Biosynthetic Link Leading to the Hetidine and Arcutine C20-Diterpenoid Alkaloids or an Oxidative Degradation Product?Modular Terpenoid Construction via Catalytic Enantioselective Formation of All-Carbon Quaternary Centers: Total Synthesis of Oridamycin A, Triptoquinones B and C, and Isoiresin.Crystallization and preliminary X-ray diffraction analysis of cyclolavandulyl diphosphate synthase, a new member of the cis-isoprenyl diphosphate synthase superfamily.Cyclobutane-1,3-Diacid (CBDA): A Semi-Rigid Building Block Prepared by [2+2] Photocyclization for Polymeric Materials.Rhodosporidium toruloides: a new platform organism for conversion of lignocellulose into terpene biofuels and bioproducts.Total synthesis of vinigrol.Identification and characterization of bacterial diterpene cyclases that synthesize the cembrane skeleton.Total synthesis: towards artificial terpene cyclases.Engineering yeast metabolism for production of terpenoids for use as perfume ingredients, pharmaceuticals and biofuels.Divergent Asymmetric Total Synthesis of Mulinane Diterpenoids.An Enyne Cope Rearrangement Enables Polycycloalkane Synthesis from Readily Available Starting Materials.A Concise Route to the Strongylophorines.Regiodivergent Remote Arylation of Cycloalkanols to Dysideanone's Fused Carbotetracycles and Its Bridged Isomers.Et3B-mediated two- and three-component coupling reactions via radical decarbonylation of α-alkoxyacyl tellurides: single-step construction of densely oxygenated carboskeletons.
P2860
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P2860
Modern synthetic efforts toward biologically active terpenes.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Modern synthetic efforts toward biologically active terpenes.
@en
type
label
Modern synthetic efforts toward biologically active terpenes.
@en
prefLabel
Modern synthetic efforts toward biologically active terpenes.
@en
P356
P1476
Modern synthetic efforts toward biologically active terpenes.
@en
P2093
Phil S Baran
Thomas J Maimone
P2888
P304
P356
10.1038/NCHEMBIO.2007.1
P577
2007-07-01T00:00:00Z
P5875
P6179
1025191053