Syntheses of sulfur and selenium analogues of pachastrissamine via double displacements of cyclic sulfate.

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Synthesis and biological evaluation of carbocyclic analogues of pachastrissamine.Formation of tetrahydrofurans via a 5-endo-tet cyclization of aziridines--synthesis of (-)-pachastrissamine.

P2860

Q35131477-EE63D508-9940-4B59-A201-F40F9EEFB69B Q43922506-82117DA1-FF5D-4375-A4D3-BE9576D7EB60

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Syntheses of sulfur and selenium analogues of pachastrissamine via double displacements of cyclic sulfate.

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http://www.wikidata.org/entity/Q39481896

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2011 nî lūn-bûn

@nan

2011年の論文

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2011年学术文章

@wuu

2011年学术文章

@zh-cn

2011年学术文章

@zh-hans

2011年学术文章

@zh-my

2011年学术文章

@zh-sg

2011年學術文章

@yue

2011年學術文章

@zh

2011年學術文章

@zh-hant

name

Syntheses of sulfur and seleni ...... splacements of cyclic sulfate.

@en

Syntheses of sulfur and seleni ...... splacements of cyclic sulfate.

@nl

type

Item

label

Syntheses of sulfur and seleni ...... splacements of cyclic sulfate.

@en

Syntheses of sulfur and seleni ...... splacements of cyclic sulfate.

@nl

prefLabel

Syntheses of sulfur and seleni ...... splacements of cyclic sulfate.

@en

Syntheses of sulfur and seleni ...... splacements of cyclic sulfate.

@nl

P1476

Syntheses of sulfur and seleni ...... isplacements of cyclic sulfate

@en

P2093

Deukjoon Kim

http://www.w3.org/2001/XMLSchema#string

Dong Jae Baek

http://www.w3.org/2001/XMLSchema#string

Hoon Bae

http://www.w3.org/2001/XMLSchema#string

Sanghee Kim

http://www.w3.org/2001/XMLSchema#string

Young-Shin Kwak

http://www.w3.org/2001/XMLSchema#string

P2860

Design, synthesis, and binding of homologated truncated 4'-thioadenosine derivatives at the human A3 adenosine receptors

Synthesis and biophysical characterization of oligonucleotides containing a 4'-selenonucleotide.

Synthesis of cytotoxic aza analogues of jaspine B.

Flexible and enantioselective access to jaspine B and biologically active chain-modified analogues thereof.

Discovery of a new template for anticancer agents: 2'-deoxy-2'-fluoro-4'-selenoarabinofuranosyl-cytosine (2'-F-4'-seleno-ara-C).

The natural marine anhydrophytosphingosine, Jaspine B, induces apoptosis in melanoma cells by interfering with ceramide metabolism.

Synthesis and biological properties of Pachastrissamine (jaspine B) and diastereoisomeric jaspines.

Ring-construction/stereoselective functionalization cascade: total synthesis of pachastrissamine (jaspine B) through palladium-catalyzed bis-cyclization of propargyl chlorides and carbonates.

Stereoselective divergent synthesis of four diastereomers of pachastrissamine (jaspine B).

Enantioselective syntheses of pachastrissamine and jaspine A via hydroxylactonization of a chiral epoxy ester.

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7237-7242

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scholarly article

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10.1039/C1OB05920C

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Hongjun Jeon

P577

2011-08-30T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

21879131

http://www.w3.org/2001/XMLSchema#string

Syntheses of sulfur and selenium analogues of pachastrissamine via double displacements of cyclic sulfate.

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P2860

P2860

Syntheses of sulfur and selenium analogues of pachastrissamine via double displacements of cyclic sulfate.

description

name

type

label

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698