Enantioselective total synthesis of the potent antitumor agent (-)-mucocin using a temporary silicon-tethered ring-closing metathesis cross-coupling reaction.
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Recent progress on the total synthesis of acetogenins from AnnonaceaeThe direct oxidative diene cyclization and related reactions in natural product synthesisStereodivergent construction of cyclic ethers by a regioselective and enantiospecific rhodium-catalyzed allylic etherification: total synthesis of gaur acid.Bi(OTf)3-, TfOH-, and TMSOTf-mediated, one-pot epoxide rearrangement, addition, and intramolecular silyl-modified Sakurai (ISMS) cascade toward dihydropyrans: comparison of catalysts and role of Bi(OTf)3Total Synthesis of Amphidinolide E and Amphidinolide E StereoisomersDivalent and Multivalent Activation in Phosphate Triesters: A Versatile Method for the Synthesis of Advanced Polyol Synthons.Total synthesis of (-)-mucocin.Improved synthesis of 6-epi-dictyostatin and antitumor efficacy in mice bearing MDA-MB231 human breast cancer xenografts.Synthesis and antitumor activity of C-9 epimers of the tetrahydrofuran containing acetogenin 4-deoxyannoreticuin.Applications of bismuth(III) compounds in organic synthesis.Temporary silicon-tethered ring-closing metathesis: recent advances in methodology development and natural product synthesis.New trends in bismuth-catalyzed synthetic transformations.Acetogenins from Annonaceae.An efficient method for synthesising unsymmetrical silaketals: substrates for ring-closing, including macrocycle-closing, metathesis.A highly convergent synthesis of the C1-C31 polyol domain of amphidinol 3 featuring a TST-RCM reaction: confirmation of the revised relative stereochemistry.Regio- and Stereoselective Homologation of 1,2-Bis(Boronic Esters): Stereocontrolled Synthesis of 1,3-Diols and Sch 725674Observations in the Synthesis of the Core of the Antitumor Illudins via an Enyne Ring Closing Metathesis CascadeA central strategy for converting natural products into fluorescent probes.Synthesis of the non-classical acetogenin mucocin: a modular approach based on olefinic coupling reactions.
P2860
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P2860
Enantioselective total synthesis of the potent antitumor agent (-)-mucocin using a temporary silicon-tethered ring-closing metathesis cross-coupling reaction.
description
2003 nî lūn-bûn
@nan
2003 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Enantioselective total synthes ...... hesis cross-coupling reaction.
@ast
Enantioselective total synthes ...... hesis cross-coupling reaction.
@en
Enantioselective total synthesis of the potent antitumor agent
@nl
type
label
Enantioselective total synthes ...... hesis cross-coupling reaction.
@ast
Enantioselective total synthes ...... hesis cross-coupling reaction.
@en
Enantioselective total synthesis of the potent antitumor agent
@nl
prefLabel
Enantioselective total synthes ...... hesis cross-coupling reaction.
@ast
Enantioselective total synthes ...... hesis cross-coupling reaction.
@en
Enantioselective total synthesis of the potent antitumor agent
@nl
P2093
P2860
P356
P1476
Enantioselective total synthes ...... hesis cross-coupling reaction.
@en
P2093
Alexei Polosukhin
Hai-Ren Zhang
P Andrew Evans
Santosh J Gharpure
P2860
P304
14702-14703
P356
10.1021/JA0384734
P407
P577
2003-12-01T00:00:00Z