Search Results - "Zuosheng Liu"
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1
Au(I)-Catalyzed Annulation of Enantioenriched Allenes in the Enantioselective Total Synthesis of (−)-Rhazinilam
Published in Journal of the American Chemical Society (16-08-2006)“…Highly stereoselective Au(I)-catalyzed pyrrole additions to enantioenriched allenes afford a unique entry to optically active heterocycles. Asymmetric…”
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Journal Article -
2
Exploratory Studies Aimed at a Synthesis of Vinigrol. 2. Attempts to Exploit Ring-Closing Metathesis for Construction of the Central Cyclooctane Belt
Published in Journal of organic chemistry (21-01-2005)“…A program directed to the possible adaptation of ring closing metathesis to a total synthesis of vinigrol is described. With a convenient route to…”
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Journal Article -
3
Exploratory Studies Aimed at a Synthesis of Vinigrol. 4. Probe of Possible Means for Direct Connection of the Side Arms and of Ring-Contraction Alternatives
Published in Journal of organic chemistry (21-01-2005)“…Attempts have been made to gain access to the vinigrol structural framework by way of three routes. These include reductive transannular cyclization,…”
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4
Three-color two-photon three-axis digital scanned light-sheet microscopy (3C2P3A-DSLM)
Published in 2015 Conference on Lasers and Electro-Optics (CLEO) (01-05-2015)“…We demonstrate a new two-photon light-sheet microscopy with three-color excitation, diffraction-limited thickness and tailorable illumination area, capable of…”
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Conference Proceeding -
5
High power 780 nm femtosecond fiber laser
Published in 2015 Conference on Lasers and Electro-Optics (CLEO) (01-05-2015)“…We demonstrate an 880 mW 780 nm femtosecond laser based on a high-order dispersion compensated Er-doped fiber laser and frequency doubling. It has been used on…”
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Conference Proceeding -
6
Synthetic Studies Aimed at (−)-Cochleamycin A. Evaluation of Late-Stage Macrocyclization Alternatives
Published in Journal of organic chemistry (17-09-2004)“…An efficient route to the fully functionalized ABC ring systems of the unnatural enantiomer of cochleamycin A was developed. l-(−)-Malic and l-(−)-ascorbic…”
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Journal Article -
7
Discovery of 2-amino-6-carboxamidobenzothiazoles as potent Lck inhibitors
Published in Bioorganic & medicinal chemistry (01-04-2008)“…A novel series of 2-amino-6-carboxamidobenzothiazole was discovered to have potent Lck inhibitory properties. A highly efficient chemistry was developed. Many…”
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8
Competitive Stereochemical Control Operative during Conrotatory Electrocyclization of Helically Equilibrating Diquinanyl-Substituted 1,3,5,7-Octatetraenyl Bisenolates
Published in Journal of organic chemistry (30-09-2005)“…Activation of the squarate ester cascade by adding the lithiated bicyclo[3.3.0]octene 20 and vinyllithium sequentially to 1 results in the isolation of the…”
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9
Synthesis of β-Amino-α-hydroxy Esters and β-Amino-α-azido Ester by Sharpless Asymmetric Aminohydroxylation, Byproducts Analysis
Published in Journal of organic chemistry (01-04-2005)“…Synthesis of enantiomerically pure β-amino-α-hydroxy esters (1, 2) and β-amino-α-azido ester (3) using Sharpless AA as a key step is described. A hitherto…”
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10
Design and synthesis of macrocycles active against vancomycin-resistant enterococci (VRE): the interplay between d-Ala- d-Lac binding and hydrophobic effect
Published in Bioorganic & medicinal chemistry letters (01-02-2005)“…[Display omitted] A modified vancomycin binding pocket (D–O–E ring) incorporating a CHNHCOR function at the AA4 position is designed and synthesized. Potent…”
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Journal Article -
11
Identification of synthetic compounds active against VRE: the role of the lipidated aminoglucose and the structure of glycopeptide binding pocket
Published in Bioorganic & medicinal chemistry letters (15-10-2005)“…Synthesis of modified vancomycin binding pocket (D–O–E ring) incorporating a ( R)- or ( S)-configured secondary alcohol function at the AA4 position is…”
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12
An efficient total synthesis of (±)-sinulariol-B
Published in Tetrahedron (1999)“…The first total synthesis of (±)-Sinulariol-B, a marine cembrandiol, was achieved in ten steps and ∼10% overall yield from E-geraniol ( 8). The key steps were…”
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13
First Total Synthesis of (+)-Caparratriene
Published in Chemistry letters (01-03-1997)“…Caparratriene (1), a new sesquiterpene hydrocarbon with significant growth inhibitory activity against CEM leukemia cells, was first synthesized starting from…”
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Journal Article -
14
Discovery of GNF-5837, a Selective TRK Inhibitor with Efficacy in Rodent Cancer Tumor Models
Published in ACS medicinal chemistry letters (09-02-2012)“…Neurotrophins and their receptors (TRKs) play key roles in the development of the nervous system and the maintenance of the neural network. Accumulating…”
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Journal Article -
15
First total synthesis of three cembrene diterpenoids
Published in Tetrahedron: asymmetry (01-10-1996)“…The first total synthesis of three diterpenoids of the cembrane class, is described. And the absolute stereochemistry of these natural products is assigned by…”
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16
Design and Synthesis of Simple Macrocycles Active Against Vancomycin-Resistant Enterococci (VRE)
Published in Chemistry : a European journal (05-07-2006)“…16‐membered meta,para‐cyclophanes mimicking the vancomycin binding pocket (D–O–E ring) were designed and synthesized. The structural key features of these…”
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17
Facile one-pot transformation of 2,3-epoxy alcohols into allylic alcohols: first total synthesis of (−)-4- O-(6′-hydroxy-7′(9′)-dehydro-6′,7′-dihydrogeranyl)coniferol
Published in Tetrahedron: asymmetry (06-11-1998)“…An efficient and practical synthesis of optically active allylic alcohols from 2,3-epoxy alcohols by the in situ formation of the epoxy iodides and their…”
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18
First enantioselective total synthesis of (−)-13-hydroxyneocembrene
Published in Tetrahedron letters (08-01-2001)“…The first enantioselective total synthesis of (−)-13-hydroxyneocembrene ( 1 ), a naturally occurring cembranoids isolated from soft coral Sarcophyton…”
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19
Enantioselective total synthesis of (+)-3,4-epoxycembrene-A
Published in Tetrahedron: asymmetry (05-02-2001)“…A concise and efficient total synthesis of (+)-3,4-epoxycembrene-A 1, an epoxy cembrane diterpenoid from tropical marine soft coral, is described. The…”
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First total synthesis and absolute configuration of marine cembrane diterpenoid (+)-11,12-epoxysarcophytol A
Published in Tetrahedron letters (27-03-2000)“…A concise and efficient total synthesis of (+)-11,12-epoxysarcophytol A ( 1), an epoxy cembrane diterpenoid from marine soft coral Lobophytum, is described,…”
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