Direct, Mild, and General n-Bu4NBr-Catalyzed Aldehyde Allylsilylation with Allyl Chlorides.

about

Design and 22-step synthesis of highly potent D-ring modified and linker-equipped analogs of spongistatin 1

P2860

Q58568333-FD3941D5-9AE6-4745-897C-8119EF3298C6

P2860

Direct, Mild, and General n-Bu4NBr-Catalyzed Aldehyde Allylsilylation with Allyl Chlorides.

Item

http://www.wikidata.org/entity/Q52453693

description

2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

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2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Direct, Mild, and General n-Bu ...... lylation with Allyl Chlorides.

@en

Direct, Mild, and General n-Bu ...... lylation with Allyl Chlorides.

@nl

type

Item

label

Direct, Mild, and General n-Bu ...... lylation with Allyl Chlorides.

@en

Direct, Mild, and General n-Bu ...... lylation with Allyl Chlorides.

@nl

prefLabel

Direct, Mild, and General n-Bu ...... lylation with Allyl Chlorides.

@en

Direct, Mild, and General n-Bu ...... lylation with Allyl Chlorides.

@nl

P1476

Direct, Mild, and General n-Bu ...... ilylation with Allyl Chlorides

@en

P2093

Isaac F Hughes

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

Kevin S Williamson

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

Makeda A Tekle-Smith

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

P2860

A new and more powerfully activating diamine for practical and scalable enantioselective aldehyde crotylsilylation reactions.

Diastereo- and enantioselective anti-alkoxyallylation employing allylic gem-dicarboxylates as allyl donors via iridium-catalyzed transfer hydrogenation.

anti-Diastereo- and enantioselective carbonyl (hydroxymethyl)allylation from the alcohol or aldehyde oxidation level: allyl carbonates as allylmetal surrogates.

Iridium-catalyzed anti-diastereo- and enantioselective carbonyl (trimethylsilyl)allylation from the alcohol or aldehyde oxidation level.

Iridium-catalyzed anti-diastereo- and enantioselective carbonyl (α-trifluoromethyl)allylation from the alcohol or aldehyde oxidation level.

Enantioselective iridium-catalyzed carbonyl allylation from the alcohol or aldehyde oxidation level using allyl acetate as an allyl metal surrogate

Enantioselective iridium-catalyzed carbonyl allylation from the alcohol or aldehyde oxidation level via transfer hydrogenative coupling of allyl acetate: departure from chirally modified allyl metal reagents in carbonyl addition

A more comprehensive and highly practical solution to enantioselective aldehyde crotylation

A "methyl extension" strategy for polyketide natural product linker site validation and its application to dictyostatin.

Enantioselective synthesis of 2-methyl-1,2-syn- and 2-methyl-1,2-anti-3-butenediols via allene hydroboration-aldehyde allylboration reaction sequences

P304

6024-6027

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scholarly article

P356

10.1021/ACS.ORGLETT.7B03193

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English

P433

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

P478

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

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James L Leighton

P577

2017-11-01T00:00:00Z

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29068688

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P932

5693333

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

Direct, Mild, and General n-Bu4NBr-Catalyzed Aldehyde Allylsilylation with Allyl Chlorides.

about

P2860

P2860

Direct, Mild, and General n-Bu4NBr-Catalyzed Aldehyde Allylsilylation with Allyl Chlorides.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932