about
Radicals: Reactive Intermediates with Translational PotentialNineteen-step total synthesis of (+)-phorbolShort, Enantioselective Total Synthesis of Highly Oxidized TaxanesAxinellamines as broad-spectrum antibacterial agents: scalable synthesis and biology.An approach to the site-selective deoxygenation of hydroxy groups based on catalytic phosphoramidite transferCatalytic enantioselective synthesis of quaternary carbon stereocentresOrigins of regio- and stereochemistry in type 2 intramolecular N-acylnitroso Diels-Alder reactions: a computational study of tether length and substituent effects.Scalable Synthesis of (-)-Thapsigargin.Microbial production of isoprenoids enabled by synthetic biology.Natural product synthesis in the age of scalability.Natural and engineered production of taxadiene with taxadiene synthase.A practical and catalytic reductive olefin coupling.Carbon-atom wires: 1-D systems with tunable properties.Two-phase synthesis of (-)-taxuyunnanine D.Scaffold Diversity Synthesis and Its Application in Probe and Drug Discovery.Synthesis of marmycin A and investigation into its cellular activity.Crystal structures of (±)-(1SR,5SR,6SR,7SR,10SR,11SR,13RS,14SR)-13-hy-droxy-7-meth-oxy-meth-oxy-11,15,18,18-tetra-methyl-3-oxo-2,4-dioxa-tetra-cyclo-[12.3.1.0(1,5).0(6,11)]octa-dec-15-en-10-yl benzoate, its 13-epimer and 13-one derivative.A multicomponent Ni-, Zr-, and Cu-catalyzed strategy for enantioselective synthesis of alkenyl-substituted quaternary carbons.Heterologous fermentation of a diterpene from Alternaria brassisicola.Enantioselective synthesis of quaternary carbon stereogenic centers through copper-catalyzed conjugate additions of aryl- and alkylaluminum reagents to acyclic trisubstituted enonesAcyclic quaternary centers from asymmetric conjugate addition of alkylzirconium reagents to linear trisubstituted enones.Total synthesis of taxane terpenes: cyclase phase.Cascade Metathesis Reactions for the Synthesis of Taxane and Isotaxane Derivatives.Selective Synthesis of Cyclooctanoids by Radical Cyclization of Seven-Membered Lactones: Neutron Diffraction Study of the Stereoselective Deuteration of a Chiral Organosamarium Intermediate.Mukaiyama Aldol Reactions in Aqueous Media.Natural product synthesis: changes over time.Formation of quaternary centers by copper-catalyzed asymmetric conjugate addition of alkylzirconium reagents.Copper-catalyzed asymmetric conjugate addition of alkylzirconium reagents to cyclic enones to form quaternary centers.Making Fe(BPBP)-catalyzed C-H and C[double bond, length as m-dash]C oxidations more affordable.Conformational Bias by a Removable Silyl Group: Construction of Bicyclo[n.3.1]alkenes by Ring Closing Metathesis.Biocatalytic conversion of cyclic ketones bearing alpha-quaternary stereocenters to lactones in an enantioselective radical approach to medium-sized carbocycles.Natural products as inspiration for the development of new synthetic methods.Domino intramolecular Diels-Alder reactions to construct a 6/6/5/5 fused tetracyclic framework.The four-step total synthesis of (-)-chaetominine.Bioinspired total syntheses of terpenoids.Complexity generation by chemical synthesis: a five-step synthesis of (-)-chaetominine from L-tryptophan and its biosynthetic implications.Accessing low-oxidation state taxanes: is taxadiene-4(5)-epoxide on the taxol biosynthetic pathway?Sustainable Syntheses of (-)-Jerantinines A & E and Structural Characterisation of the Jerantinine-Tubulin Complex at the Colchicine Binding Site.A practical deca-gram scale ring expansion of (R)-(−)-carvone to (R)-(+)-3-methyl-6-isopropenyl-cyclohept-3-enone-1Hazel and other sources of paclitaxel and related compounds
P2860
Q28468198-188BD5DA-CAC6-4D80-B4BC-E7E8B73F45D3Q28834634-BC53EF6B-4C21-45BA-BEFB-C5FCFD04AAE1Q29041697-94D279BD-68E6-4001-8F4F-31A46C25432EQ34489878-F3EDAD40-C69B-4DF7-899C-1884C2D19C1DQ35871115-53839F00-73AA-46BA-ABED-607C29F0A095Q36420603-EC2A732C-E483-4448-A275-7EBC7AD2FDB1Q36802661-02EAF99B-F530-4DFB-B084-77DA3F8E52E5Q37609381-8E220E8B-5531-445C-AC3D-C69F092B50A6Q38098175-CE7F0D59-B23B-4D31-9913-454469595A17Q38171270-439DB44B-998E-450D-8DC6-B84694DE4250Q38254517-2B2555CC-85F5-4300-B52B-54C7E31EA4D1Q38579982-7FD75C3B-1A89-40DA-863D-AD526454B38FQ38723632-372828DF-9058-4360-8587-05EBFD8AEC8FQ38738372-20B90CCA-97E8-4DEA-B7CE-56F1EBCC97FEQ38836332-6EDAE4C2-DDC5-4F7C-94C8-1F51841E1FECQ38842272-18AC8122-E921-476E-9E77-582F6D1A04B9Q40278778-E36DD87F-747A-4956-B247-25396515A7ACQ40435109-2C05C4E2-C1B3-4F96-ABD7-E34ACD4BC4DAQ42001894-779227A3-34BB-4CB3-AB83-C886F6B7E81BQ42007847-C210F93F-3D08-4504-8C38-8DD2E76E1334Q42029518-2C36D20D-CE37-48C4-994D-8E663E9F24AAQ42164644-0605F602-3E71-4FEF-AA6B-50BA4229B214Q42362195-270E5398-9253-4745-A0FB-A1DF9819D420Q42366740-D33D1512-D2D7-4BCE-936F-F2049C95D99EQ42704003-6D94888B-7F70-49C3-BA44-FE815385EA1EQ44012719-4B803E77-294B-4545-946B-CBF9F9E8F295Q44137961-4A851BF7-2889-41F3-994A-CF7877B1A877Q44668565-46A5F893-5D84-4446-976D-D74930493F4DQ46943514-110804C0-A1E2-492A-90DE-1CC39C7A2246Q47366712-1738584B-9208-4CE8-A868-79C994D84FF9Q49375340-8DD60136-0A5D-4B4C-B412-5B2F9BED4E57Q50074167-1CBAAC0C-33DE-4325-B2F1-1824B8FBA171Q50924861-90E99E0C-1738-42A8-AAFD-E03840836D58Q51759290-D29C1900-7BBD-4215-8AAA-688EC4AFE3DEQ52788019-7B011EE6-100C-4BF7-A2DF-7C1B8C8E05CAQ53588509-3915A578-B8ED-4597-9DC2-393EE76AEAFDQ55607552-C21FEC58-1958-4ED3-84F8-2979E1841CB6Q55710225-B6BBF101-3AC0-4CC3-B804-7D65070BD6AEQ56951465-77E36523-2509-4FAB-A592-D3D696013E94Q57003263-F422FCF8-3FBC-4370-B174-9A3D64810A88
P2860
description
2012 nî lūn-bûn
@nan
2012 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Scalable enantioselective total synthesis of taxanes
@ast
Scalable enantioselective total synthesis of taxanes
@en
Scalable enantioselective total synthesis of taxanes
@nl
type
label
Scalable enantioselective total synthesis of taxanes
@ast
Scalable enantioselective total synthesis of taxanes
@en
Scalable enantioselective total synthesis of taxanes
@nl
prefLabel
Scalable enantioselective total synthesis of taxanes
@ast
Scalable enantioselective total synthesis of taxanes
@en
Scalable enantioselective total synthesis of taxanes
@nl
P2093
P2860
P3181
P356
P1433
P1476
Scalable enantioselective total synthesis of taxanes
@en
P2093
Abraham Mendoza
Phil S Baran
Yoshihiro Ishihara
P2860
P2888
P3181
P356
10.1038/NCHEM.1196
P407
P577
2012-01-01T00:00:00Z
P5875
P6179
1002103811