Pd-catalyzed nucleophilic alkylation of aliphatic aldehydes with allyl alcohols: allyl, 2-tetrahydrofuryl, and 2-tetrahydropyranyl ethers as useful C3, C4, and C5 sources.

Pd-catalyzed nucleophilic alkylation of aliphatic aldehydes with allyl alcohols: allyl, 2-tetrahydrofuryl, and 2-tetrahydropyranyl ethers as useful C3, C4, and C5 sources.

Item
http://www.wikidata.org/entity/Q44531127
Enantioselective iridium-catalyzed carbonyl allylation from the alcohol or aldehyde oxidation level using allyl acetate as an allyl metal surrogateEnantioselective 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 additionFormation of C-C Bonds via Catalytic Hydrogenation and Transfer Hydrogenation: Vinylation, Allylation, and Enolate Addition of Carbonyl Compounds and IminesCatalytic carbonyl addition through transfer hydrogenation: a departure from preformed organometallic reagents.Enantioselective iridium-catalyzed carbonyl allylation from the alcohol oxidation level via transfer hydrogenation: minimizing pre-activation for synthetic efficiencyFormation of C-C Bonds via Iridium-Catalyzed Hydrogenation and Transfer Hydrogenation.anti-Diastereo- and enantioselective carbonyl crotylation from the alcohol or aldehyde oxidation level employing a cyclometallated iridium catalyst: alpha-methyl allyl acetate as a surrogate to preformed crotylmetal reagents.1,n-glycols as dialdehyde equivalents in iridium-catalyzed enantioselective carbonyl allylation and iterative two-directional assembly of 1,3-polyols.Pd-catalyzed diastereoselective allylation of aldehydes with 3-bromomethyl-5H-furan-2-one: stereoselective synthesis of β-(hydroxymethylaryl/alkyl)-α-methylene-γ-butyrolactones with a syn configuration.Nickel-Catalyzed α-Allylation of Aldehydes and Tandem Aldol Condensation/Allylation Reaction with Allylic Alcohols.Catalytic nucleophilic 'umpoled' π-allyl reagents.
P2860

Pd-catalyzed nucleophilic alkylation of aliphatic aldehydes with allyl alcohols: allyl, 2-tetrahydrofuryl, and 2-tetrahydropyranyl ethers as useful C3, C4, and C5 sources.

Item
http://www.wikidata.org/entity/Q44531127
description
2003 nî lūn-bûn
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2003年の論文
@ja
2003年学术文章
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2003年学术文章
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2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
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2003年學術文章
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2003年學術文章
@zh-hant
name
Pd-catalyzed nucleophilic alky ...... useful C3, C4, and C5 sources.
@en
Pd-catalyzed nucleophilic alky ...... useful C3, C4, and C5 sources.
@nl
type
label
Pd-catalyzed nucleophilic alky ...... useful C3, C4, and C5 sources.
@en
Pd-catalyzed nucleophilic alky ...... useful C3, C4, and C5 sources.
@nl
prefLabel
Pd-catalyzed nucleophilic alky ...... useful C3, C4, and C5 sources.
@en
Pd-catalyzed nucleophilic alky ...... useful C3, C4, and C5 sources.
@nl
P1433
P1476
P2093
P304
P31
P356
P407
P433
P478
P50
P577
P698
P356
P1433
P1476
Pd-catalyzed nucleophilic alky ...... useful C3, C4, and C5 sources.
@en
P2093
P304
P31
P356
P407
P433
P478
P50
P577
P698