Catalytic enantioselective alkylation of aldehydes by using organozinc halide reagents.

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Catalytic enantioselective synthesis of α-substituted secondary allylic alcohols from terminal alkynes and aldehydes via vinylaluminum reagents.Development of Highly Active Chiral Titanium Catalysts for the Enantioselective Addition of Various Organometallic Reagents to Aldehydes.

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P2860

Catalytic enantioselective alkylation of aldehydes by using organozinc halide reagents.

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http://www.wikidata.org/entity/Q44450932

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2013 nî lūn-bûn

@nan

2013年の論文

@ja

2013年学术文章

@wuu

2013年学术文章

@zh

2013年学术文章

@zh-cn

2013年学术文章

@zh-hans

2013年学术文章

@zh-my

2013年学术文章

@zh-sg

2013年學術文章

@yue

2013年學術文章

@zh-hant

name

Catalytic enantioselective alkylation of aldehydes by using organozinc halide reagents.

@en

Catalytic enantioselective alkylation of aldehydes by using organozinc halide reagents.

@nl

type

Item

label

Catalytic enantioselective alkylation of aldehydes by using organozinc halide reagents.

@en

Catalytic enantioselective alkylation of aldehydes by using organozinc halide reagents.

@nl

prefLabel

Catalytic enantioselective alkylation of aldehydes by using organozinc halide reagents.

@en

Catalytic enantioselective alkylation of aldehydes by using organozinc halide reagents.

@nl

P1476

Catalytic enantioselective alkylation of aldehydes by using organozinc halide reagents.

@en

P2093

Shinichi Kanehira

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Toshiro Harada

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

Yasuki Hayashi

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

Yuichiro Kinoshita

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P2860

Efficient Synthesis of Functionalized Organozinc Compounds by the Direct Insertion of Zinc into Organic Iodides and Bromides

Activation of functional arylzincs prepared from aryl iodides and highly enantioselective addition to aldehydes.

Facile synthesis of a family of H8BINOL-amine compounds and catalytic asymmetric arylzinc addition to aldehydes.

Exposing the hidden complexity of stoichiometric and catalytic metathesis reactions by elucidation of Mg-Zn hybrids.

Titanium-catalyzed enantioselective additions of alkyl groups to aldehydes: mechanistic studies and new concepts in asymmetric catalysis.

Highly stereoselective total synthesis of fully hydroxy-protected mycolactones A and B and their stereoisomerization upon deprotection

Insight into the mechanism of the asymmetric addition of alkyl groups to aldehydes catalyzed by titanium-BINOLate species.

Catalyzed asymmetric aryl transfer reactions to aldehydes with boronic acids as aryl source.

Catalytic asymmetric aryl transfer reactions to aldehydes with Grignard reagents as the aryl source.

Preparation of Functionalized Dialkylzincs via a Boron−Zinc Exchange. Reactivity and Catalytic Asymmetric Addition to Aldehydes

P304

3311-3314

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scholarly article

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10.1002/CHEM.201204346

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English

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P478

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

P577

2013-02-05T00:00:00Z

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P698

23386512

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P921

enantioselectivity

Catalytic enantioselective alkylation of aldehydes by using organozinc halide reagents.

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P2860

P2860

Catalytic enantioselective alkylation of aldehydes by using organozinc halide reagents.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P921