Diastereo- and Enantioselective Reductive Aldol Addition of Vinyl Ketones via Catalytic Hydrogenation
about
Stereoselective synthesis of highly functionalized alpha-diazo-beta-ketoalkanoates via catalytic one-pot Mukaiyama-Aldol reactionsL-selectride-mediated highly diastereoselective asymmetric reductive aldol reaction: access to an important subunit for bioactive moleculesBroad Spectrum Enolate Equivalent for Catalytic Chemo-, Diastereo-, and Enantioselective Addition to N-Boc Imines.(Diisopinocampheyl)borane-mediated reductive aldol reactions of acrylate esters: enantioselective synthesis of anti-aldolsDiisopinocampheylborane-mediated reductive aldol reactions: highly enantio- and diastereoselective synthesis of syn aldols from N-acryloylmorpholine.Generation of stereochemically defined tetrasubstituted enolborinates by 1,4-hydroboration of α,β-unsaturated morpholine carboxamides with (diisopinocampheyl)borane.The 'LipoYeasts' project: using the oleaginous yeast Yarrowia lipolytica in combination with specific bacterial genes for the bioconversion of lipids, fats and oils into high-value products.Unlocking Hydrogenation for C-C Bond Formation: A Brief Overview of Enantioselective Methods.1,n-glycols as dialdehyde equivalents in iridium-catalyzed enantioselective carbonyl allylation and iterative two-directional assembly of 1,3-polyols.Enantioselective carbonyl reverse prenylation from the alcohol or aldehyde oxidation level employing 1,1-dimethylallene as the prenyl donorEnantioselective allylation, crotylation, and reverse prenylation of substituted isatins: iridium-catalyzed C-C bond-forming transfer hydrogenation.
P2860
Q33692906-1BB9BB35-F20B-4295-A3B1-7C7569FF1463Q34147340-58F78906-78FD-4D6A-A07E-9E99A66E19EFQ36900345-6C25E1B3-4509-4BD3-A3EB-E253427F4582Q37172120-B05712EB-86B2-48C6-96B8-4843B5C1B7D2Q37268017-E2227459-42D4-4D11-BF1D-6A47C7EADE81Q37542796-319BA0E0-919A-4A7E-AA90-8118499DF884Q37831423-1FBCCAAE-E4C6-47DF-AC2E-C3084CF3945BQ39372722-842B25E3-2D22-48D3-934E-DA740EDBA6FCQ39752033-41786B3D-4C63-4420-B8FD-359CA4DB7545Q39775784-A5FB7A50-921F-49E7-9472-83DE991494ABQ39831735-8AC5FFD7-0C8E-4D84-8999-5946CC302852
P2860
Diastereo- and Enantioselective Reductive Aldol Addition of Vinyl Ketones via Catalytic Hydrogenation
description
2008 nî lūn-bûn
@nan
2008 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Diastereo- and Enantioselectiv ...... es via Catalytic Hydrogenation
@ast
Diastereo- and Enantioselectiv ...... es via Catalytic Hydrogenation
@en
type
label
Diastereo- and Enantioselectiv ...... es via Catalytic Hydrogenation
@ast
Diastereo- and Enantioselectiv ...... es via Catalytic Hydrogenation
@en
prefLabel
Diastereo- and Enantioselectiv ...... es via Catalytic Hydrogenation
@ast
Diastereo- and Enantioselectiv ...... es via Catalytic Hydrogenation
@en
P2860
P356
P1433
P1476
Diastereo- and Enantioselectiv ...... es via Catalytic Hydrogenation
@en
P2093
Abbas Hassan
Soo Bong Han
P2860
P304
P356
10.1055/S-2008-1067220
P577
2008-09-01T00:00:00Z