Enantioselective access to benzannulated spiroketals using a chiral sulfoxide auxiliary.

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Isolation, biological activity, biosynthesis and synthetic studies towards the rubromycin family of natural products.Designed Spiroketal Protein Modulation.Designed Spiroketal Protein Modulation

P2860

Q38387308-3EEA50EB-C5F6-4BC9-B316-F88D920CE362 Q42259127-592194F3-C456-44BC-AC17-904D6426D1EC Q57531344-8607048E-E12D-4047-964E-D87F0DDE26DB

P2860

Enantioselective access to benzannulated spiroketals using a chiral sulfoxide auxiliary.

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http://www.wikidata.org/entity/Q44546573

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2013 nî lūn-bûn

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2013年の論文

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年學術文章

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2013年學術文章

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Enantioselective access to benzannulated spiroketals using a chiral sulfoxide auxiliary.

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Enantioselective access to benzannulated spiroketals using a chiral sulfoxide auxiliary.

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Item

label

Enantioselective access to benzannulated spiroketals using a chiral sulfoxide auxiliary.

@en

Enantioselective access to benzannulated spiroketals using a chiral sulfoxide auxiliary.

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Enantioselective access to benzannulated spiroketals using a chiral sulfoxide auxiliary.

@en

Enantioselective access to benzannulated spiroketals using a chiral sulfoxide auxiliary.

@nl

P1476

Enantioselective access to benzannulated spiroketals using a chiral sulfoxide auxiliary.

@en

P2093

Daniel P Furkert

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

Harry R M Aitken

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

James M Wood

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

Jonathan G Hubert

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

P2860

Studies in the Total Synthesis of Heliquinomycinone: Proof of Concept and Assembly of a Fully Mature Spirocyclization Precursor This work was supported by the National Institutes of Health (Grant numbers: AI 16943 and HL25848). A Postdoctoral Fellow

Asymmetric spiroacetalization catalysed by confined Brønsted acids.

Isolation, biological activity and synthesis of benzannulated spiroketal natural products.

Facile synthesis of naphthoquinone spiroketals by diastereoselective oxidative [3 + 2] cycloaddition.

An efficient formal synthesis of the human telomerase inhibitor (+/-)-gamma-rubromycin.

A convergent total synthesis of (±)-γ-rubromycin.

Liquid-crystal engineering with anchor-shaped molecules: honeycombs with hexagonal and trigonal symmetries formed by polyphilic bent-core molecules.

Catalytic asymmetric synthesis of aromatic spiroketals by spinphox/iridium(I)-catalyzed hydrogenation and spiroketalization of α,α'-bis(2-hydroxyarylidene) ketones.

A simple enantioselective synthesis of (R)- and (S)-1,7-dioxaspiro[5.5]undecane via intramolecular asymmetric oxyselenenylation: a new route to optically active spiroketals

P304

5147-5155

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

P31

scholarly article

P356

10.1039/C3OB41065J

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

P433

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

P478

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

P50

Margaret Brimble

P577

2013-07-02T00:00:00Z

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

P698

23817587

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

P921

enantioselectivity

Enantioselective access to benzannulated spiroketals using a chiral sulfoxide auxiliary.

about

P2860

P2860

Enantioselective access to benzannulated spiroketals using a chiral sulfoxide auxiliary.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921