Azomethine Ylides from Nitrones: Using Catalytic nBuLi for the Totally Stereoselective Synthesis of trans-2-Alkyl-3-oxazolines.
about
Direct Asymmetric Aza-Vinylogous-Type Michael Additions of Nitrones from Isatins to Nitroalkenes.Coordination chemistry of mercury(ii) with 2-pyridylnitrones: monomers to polymers.Regioselectivity Change in the Organocatalytic Enantioselective (3+2) Cycloaddition with Nitrones through Cooperative Hydrogen-Bonding Catalysis/Iminium Activation.
P2860
Azomethine Ylides from Nitrones: Using Catalytic nBuLi for the Totally Stereoselective Synthesis of trans-2-Alkyl-3-oxazolines.
description
2016 nî lūn-bûn
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name
Azomethine Ylides from Nitrone ...... of trans-2-Alkyl-3-oxazolines.
@en
Azomethine Ylides from Nitrone ...... of trans-2-Alkyl-3-oxazolines.
@nl
type
label
Azomethine Ylides from Nitrone ...... of trans-2-Alkyl-3-oxazolines.
@en
Azomethine Ylides from Nitrone ...... of trans-2-Alkyl-3-oxazolines.
@nl
prefLabel
Azomethine Ylides from Nitrone ...... of trans-2-Alkyl-3-oxazolines.
@en
Azomethine Ylides from Nitrone ...... of trans-2-Alkyl-3-oxazolines.
@nl
P2093
P2860
P50
P356
P1476
Azomethine Ylides from Nitrone ...... of trans-2-Alkyl-3-oxazolines.
@en
P2093
Ignacio Delso
Pedro Merino
Tomás Tejero
Veronica Juste-Navarro
P2860
P304
11527-11532
P356
10.1002/CHEM.201602159
P407
P577
2016-06-03T00:00:00Z