Nickel-Catalyzed Homoallylation of Aldehydes in the Presence of Water and Alcohols We thank Mr. Y. Ohhama, NMR Facility, for his outstanding technical assistance. Financial support from the Ministry of Education, Science, Sports, and Culture, Japane
about
A formal synthesis of the C1-C9 fragment of amphidinolide C employing the Tamaru reaction.Iridium-catalyzed C-C coupling via transfer hydrogenation: carbonyl addition from the alcohol or aldehyde oxidation level employing 1,3-cyclohexadiene.Ruthenium-catalyzed C-C bond forming transfer hydrogenation: carbonyl allylation from the alcohol or aldehyde oxidation level employing acyclic 1,3-dienes as surrogates to preformed allyl metal reagents.Catalytic carbonyl addition through transfer hydrogenation: a departure from preformed organometallic reagents.Formation of C-C Bonds via Ruthenium Catalyzed Transfer Hydrogenation: Carbonyl Addition from the Alcohol or Aldehyde Oxidation LevelDirect ruthenium-catalyzed C-C coupling of ethanol: diene hydro-hydroxyethylation to form all-carbon quaternary centers.All-carbon quaternary centers via ruthenium-catalyzed hydroxymethylation of 2-substituted butadienes mediated by formaldehyde: beyond hydroformylationDirect, redox-neutral prenylation and geranylation of secondary carbinol C-H bonds: C4-regioselectivity in ruthenium-catalyzed C-C couplings of dienes to α-hydroxy estersRegioselective ruthenium catalyzed hydrohydroxyalkylation of dienes with 3-hydroxy-2-oxindoles: prenylation, geranylation, and beyond.Ni-catalyzed homoallylation of polyhydroxy n,o-acetals with conjugated dienes promoted by triethylborane.
P2860
Q33959314-98A263BE-BDAF-4D3F-B195-1FEDC380FA58Q34746872-B86D9406-878B-4FCD-BDF2-36463B85DCC5Q34774738-0090B55A-F17E-49BB-B267-DC05BB46A8BDQ37336741-C43B9483-2ADC-47CE-88E5-2836B2CE58FAQ38414807-ACE380B3-9B0A-43A1-BD28-95F012DE5464Q40998694-CACD4720-EB3D-4C32-8347-52AE3A709773Q42544443-BED8FF26-8EC6-4EB7-9C10-1DC84469695CQ42588665-5EBBA548-5371-42EC-9A96-31E2507B3528Q42693166-D4260727-6280-4C8E-AF25-01BD133A43B7Q53510695-5838C2CA-BF14-44F4-8A57-099F937FB9FB
P2860
Nickel-Catalyzed Homoallylation of Aldehydes in the Presence of Water and Alcohols We thank Mr. Y. Ohhama, NMR Facility, for his outstanding technical assistance. Financial support from the Ministry of Education, Science, Sports, and Culture, Japane
description
2001 nî lūn-bûn
@nan
2001 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Nickel-Catalyzed Homoallylatio ...... e, Sports, and Culture, Japane
@ast
Nickel-Catalyzed Homoallylatio ...... e, Sports, and Culture, Japane
@en
type
label
Nickel-Catalyzed Homoallylatio ...... e, Sports, and Culture, Japane
@ast
Nickel-Catalyzed Homoallylatio ...... e, Sports, and Culture, Japane
@en
prefLabel
Nickel-Catalyzed Homoallylatio ...... e, Sports, and Culture, Japane
@ast
Nickel-Catalyzed Homoallylatio ...... e, Sports, and Culture, Japane
@en
P2093
P1433
P1476
Nickel-Catalyzed Homoallylatio ...... e, Sports, and Culture, Japane
@en
P2093
Akihiro Ezoe
Masanari Kimura
Shuji Tanaka
Yoshinao Tamaru
P304
P356
10.1002/1521-3773(20011001)40:19<3600::AID-ANIE3600>3.0.CO;2-N
P577
2001-10-01T00:00:00Z