Enantioselective total synthesis of (-)-pironetin: iterative aldol reactions of thiazolidinethiones. - Wikidata - wikimedia - TriplyDB

Enantioselective total synthesis of (-)-pironetin: iterative aldol reactions of thiazolidinethiones.

Enantioselective total synthesis of (-)-pironetin: iterative aldol reactions of thiazolidinethiones.

http://www.wikidata.org/entity/Q34961575

about

Bioinspired iterative synthesis of polyketides Synthesis and Cytotoxicity Evaluation of C4- and C5-Modified Analogues of the α,β-Unsaturated Lactone of Pironetin The taumycin A macrocycle: asymmetric total synthesis and revision of relative stereochemistry.Enantioselective synthesis of the C1-C6 and C7-C23 fragments of the proposed structure of iriomoteolide 1a.Recent developments in the total synthesis of fungicidal natural products--a crop protection perspective.Synthesis and biological evaluation of truncated α-tubulin-binding pironetin analogues lacking alkyl pendants in the side chain or the dihydropyrone ring.1-[(4S)-4-Benzyl-2-thioxo-1,3-thia-zol-idin-3-yl]propan-1-one Synthesis and biological evaluation of simplified pironetin analogues with modifications in the side chain and the lactone ring.Iterative asymmetric allylic substitutions: syn- and anti-1,2-diols through catalyst control.

P2860

Q27006546-E9AB544E-4FD6-478A-92D0-8427B48CED5D Q33628649-0CD8DC64-EB5E-4FA5-95C3-179CC7581D94 Q34285982-D3715E47-A6AC-40E4-9B77-D68C124BACFA Q35936028-2F00F05A-ABE7-4FBE-A848-4DEA770E9EEE Q37834345-686BF12A-8697-4F42-B457-0119A8F46567 Q39119360-8610CDAE-36BE-4FC8-8BC4-696CB83E6DB2 Q42387052-7A5E2102-3F5A-4554-8CFC-35691C7C1249 Q51295626-BDE4FAFA-5E13-4E80-B63F-BAFCD9655626 Q53389207-F2DB5388-2C94-4654-ADC9-5A5B6013DA8B

P2860

Enantioselective total synthesis of (-)-pironetin: iterative aldol reactions of thiazolidinethiones.

http://www.wikidata.org/entity/Q34961575

description

2009 nî lūn-bûn

@nan

2009 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年論文

@yue

2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

@wuu

name

Enantioselective total synthes ...... ctions of thiazolidinethiones.

@ast

Enantioselective total synthes ...... ctions of thiazolidinethiones.

@en

type

label

Enantioselective total synthes ...... ctions of thiazolidinethiones.

@ast

Enantioselective total synthes ...... ctions of thiazolidinethiones.

@en

prefLabel

Enantioselective total synthes ...... ctions of thiazolidinethiones.

@ast

Enantioselective total synthes ...... ctions of thiazolidinethiones.

@en

P1433

Q34961575-568098DA-1CCB-4DB1-81D9-E966F577638E

P1476

Q34961575-B2576920-9DD4-439F-8389-8EE47AF06F31

P2093

Q34961575-32DF3173-8059-4755-AF90-A0BB93774240

Q34961575-EDE90133-7DC7-4DEA-BA35-6A8491574832

P2860

Q34961575-1B6D70C2-A286-43F3-8E26-D45F589930DB

Q34961575-30E0BC72-B8C6-4859-8A5C-14305F53321F

Q34961575-3C05B6B0-FB11-4B79-9F9B-609C05317CB4

Q34961575-3CDD8B99-08D1-4893-AC22-910088D2304E

Q34961575-451FFB05-983C-406F-9FFA-28EDA5CFFCA0

Q34961575-6C808F3B-A063-4E34-90C5-8D7369244029

Q34961575-72606DC8-8DD9-499A-90D8-BC01F66C243F

Q34961575-7AA46167-E932-4219-8803-1F93C080F49F

Q34961575-82B39C5A-62FB-49D3-B181-E42BC223B6B6

Q34961575-86F27A17-2A5D-4D44-A528-98A586A0A1AA

P304

Q34961575-69296631-6CEB-485A-BC50-6AED87D0A1B5

P31

Q34961575-48284DDF-5111-46C5-A144-D7F17B6F7E42

P356

Q34961575-EFC4C833-E960-4CE8-8ABA-251996A24EC9

P407

Q34961575-A76433C9-61DB-44D9-AB07-2B4A51FDC31F

P433

Q34961575-45DD2537-7CC8-4563-AEF3-C2423A78EB8D

P478

Q34961575-AA6FC7AC-61D9-4F41-980F-D091EFDC6F86

P577

Q34961575-91961F4C-0C5B-47EF-BF28-1A013FD830BF

P5875

Q34961575-28CE49FF-04D4-41D6-A2EF-4A93B416A1B6

P698

Q34961575-48D4204D-98A8-4534-BB5E-944B114E6162

P921

Q34961575-001FEB38-829C-46CE-8702-4B0EEE21903F

P932

Q34961575-3942FAB4-A3F9-469A-B594-06C96FD616A4

P356

P1433

Organic Letters

P1476

Enantioselective total synthes ...... ctions of thiazolidinethiones.

@en

P2093

Anne-Marie R Dechert

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

Michael T Crimmins

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

P2860

Highly anti-selective asymmetric aldol reactions using chiral zirconium catalysts. Improvement of activities, structure of the novel zirconium complexes, and effect of a small amount of water for the preparation of the catalysts.

Enantioselective addition of a chiral thiazolidinethione-derived titanium enolate to acetals.

Titanium enolates of thiazolidinethione chiral auxiliaries: versatile tools for asymmetric aldol additions.

Diastereoselective magnesium halide-catalyzed anti-aldol reactions of chiral N-acyloxazolidinones.

Magnesium halide-catalyzed anti-aldol reactions of chiral N-acylthiazolidinethiones.

Formal synthesis of 6-deoxyerythronolide B.

The anticancer natural product pironetin selectively targets Lys352 of alpha-tubulin.

Synthesis of pironetin and related analogs: studies on structure-activity relationships as tubulin assembly inhibitors.

Asymmetric aldol additions: use of titanium tetrachloride and (-)-sparteine for the soft enolization of N-acyl oxazolidinones, oxazolidinethiones, and thiazolidinethiones.

Pironetin, a novel plant growth regulator produced by Streptomyces sp. NK10958. I. Taxonomy, production, isolation and preliminary characterization.

P304

1635-1638

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

P31

scholarly article

P356

10.1021/OL9003228

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

P407

P433

7

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

P478

11

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

P577

2009-04-01T00:00:00Z

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

P5875

24196126

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

P698

19281219

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

P921

enantioselectivity

P932

2701212

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