Synthesis of (−)-Gloeosporone, a fungal autoinhibitor of spore germination using a π-allyltricarbonyliron lactone complex as a templating architecture for 1,7-diol construction

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Synthesis of (−)-Gloeosporone, a fungal autoinhibitor of spore germination using a π-allyltricarbonyliron lactone complex as a templating architecture for 1,7-diol construction

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http://www.wikidata.org/entity/Q56952782

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im Oktober 2003 veröffentlichter wissenschaftlicher Artikel

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scientific article published on 01 October 2003

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wetenschappelijk artikel

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наукова стаття, опублікована у 2003

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Synthesis of (−)-Gloeosporone, ...... ture for 1,7-diol construction

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Synthesis of (−)-Gloeosporone, ...... ture for 1,7-diol construction

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Synthesis of (−)-Gloeosporone, ...... ture for 1,7-diol construction

@en

Synthesis of (−)-Gloeosporone, ...... ture for 1,7-diol construction

@nl

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Synthesis of (−)-Gloeosporone, ...... ture for 1,7-diol construction

@en

Synthesis of (−)-Gloeosporone, ...... ture for 1,7-diol construction

@nl

P1476

Synthesis of (-)-gloeosporone, ...... ture for 1,7-diol construction

@en

P2093

Christopher J Hollowood

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Ed Cleator

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Jürgen Harter

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P2860

Increased ring closing metathesis activity of ruthenium-based olefin metathesis catalysts coordinated with imidazolin-2-ylidene ligands

1,7-Asymmetric induction of chirality in a Mukaiyama aldol reaction using π-allyltricarbonyliron lactone complexes: highly diastereoselective synthesis of α-substituted β-hydroxy carbonyl compounds

1,7-Induction of chirality in Mukaiyama aldol reactions using π-allyltricarbonyliron lactone and lactam complexes as chiral templates

Total synthesis of the cholesterol biosynthesis inhibitor 1233A via a (π-allyl)tricarbonyliron lactone complex

Double diastereodifferentiation in the Mukaiyama aldol reactions of π-allyltricarbonyliron lactone complexes: 1,7- vs. 1,2-asymmetric induction

Highly diastereoselective synthesis of β-hydroxy carbonyl compounds using π-allyltricarbonyliron lactone complexes: a formal 1,7-asymmetric induction of chirality in a Mukaiyama aldol reaction

Mukaiyama aldol reactions of π-allyltricarbonyliron lactone and lactam complexes bearing trimethylsilyl enol ether side-chains. Not just formal, but genuine 1,7 induction of chirality

1,5-Asymmetric induction of chirality: diastereoselective addition of organoaluminium reagents and allylstannanes into aldehyde groups in the side-chain of π-allyltricarbonyliron lactone complexes

1,5-Asymmetric induction of chirality: highly diastereoselective addition reactions of organoaluminium reagents into ketone groups in the side-chain of π-allyltricarbonyliron lactone complexes

1,5-Asymmetric induction of chirality: highly diastereoselective synthesis of homoallylic tertiary alcohols by the Lewis acid-mediated addition of allylstannanes into ketones in the side-chain of π-allyltricarbonyliron lactone complexes

P304

3263-3264

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P31

scholarly article

P356

10.1039/B308793J

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P433

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

P478

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

P50

Steven V. Ley

P577

2003-10-01T00:00:00Z

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P698

14584786

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P921

autoinhibition