Enantioselective assembly of tertiary stereocenters via multicomponent chemoselective cross-coupling of geminal chloro(iodo)alkanes.

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Enantioselective assembly of tertiary stereocenters via multicomponent chemoselective cross-coupling of geminal chloro(iodo)alkanes.

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http://www.wikidata.org/entity/Q41092159

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2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Enantioselective assembly of t ...... f geminal chloro(iodo)alkanes.

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type

Item

label

Enantioselective assembly of t ...... f geminal chloro(iodo)alkanes.

@en

prefLabel

Enantioselective assembly of t ...... f geminal chloro(iodo)alkanes.

@en

P1476

Enantioselective assembly of t ...... of geminal chloro(iodo)alkanes

@en

P2093

K Kulbitski

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

M Gandelman

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

X Jiang

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

P2860

Bond dissociation energies of organic molecules

Stereoconvergent amine-directed alkyl-alkyl Suzuki reactions of unactivated secondary alkyl chlorides

Asymmetric alkyl-alkyl cross-couplings of unactivated secondary alkyl electrophiles: stereoconvergent Suzuki reactions of racemic acylated halohydrins

The asymmetric Heck and related reactions.

Advances in transition metal (Pd, Ni, Fe)-catalyzed cross-coupling reactions using alkyl-organometallics as reaction partners

Catalytic asymmetric γ-alkylation of carbonyl compounds via stereoconvergent Suzuki cross-couplings.

New directing groups for metal-catalyzed asymmetric carbon-carbon bond-forming processes: stereoconvergent alkyl-alkyl Suzuki cross-couplings of unactivated electrophiles.

Catalytic asymmetric conjugate addition and allylic alkylation with Grignard reagents.

Asymmetric transition metal-catalyzed cross-coupling reactions for the construction of tertiary stereocenters.

Nickel complexes of a pincer NN2 ligand: multiple carbon-chloride activation of CH2Cl2 and CHCl3 leads to selective carbon-carbon bond formation.

P304

2762-2767

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P31

scholarly article

P356

10.1039/C5SC04378F

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P433

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

P478

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

P50

Gennady Nisnevitch

P577

2016-01-06T00:00:00Z

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

P698

28660053

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P921

enantioselectivity

P932

5477020

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