Regio- and Diastereoselective and Enantiospecific Metal-Free C(sp(3) )-H Arylation: Facile Access to Optically Active 5-Aryl 2,5-Disubstituted Pyrrolidines.
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Redox-Annulation of Cyclic Amines and β-Ketoaldehydes.An Ugi Reaction Incorporating a Redox-Neutral Amine C-H Functionalization StepAcetic Acid Promoted Redox Annulations with Dual C-H Functionalization.Redox-Neutral Aromatization of Cyclic Amines: Mechanistic Insights and Harnessing of Reactive Intermediates for Amine α- and β-C-H Functionalization.Iterative direct C(sp3)-H functionalization of amines: diastereoselective divergent syntheses of α,α'-disubstituted alicyclic amines.Classical-Reaction-Driven Stereo- and Regioselective C(sp(3) )-H Functionalization of Aliphatic Amines.
P2860
Regio- and Diastereoselective and Enantiospecific Metal-Free C(sp(3) )-H Arylation: Facile Access to Optically Active 5-Aryl 2,5-Disubstituted Pyrrolidines.
description
2015 nî lūn-bûn
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2015年の論文
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2015年学术文章
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2015年学术文章
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name
Regio- and Diastereoselective ...... ,5-Disubstituted Pyrrolidines.
@en
Regio- and Diastereoselective ...... ,5-Disubstituted Pyrrolidines.
@nl
type
label
Regio- and Diastereoselective ...... ,5-Disubstituted Pyrrolidines.
@en
Regio- and Diastereoselective ...... ,5-Disubstituted Pyrrolidines.
@nl
prefLabel
Regio- and Diastereoselective ...... ,5-Disubstituted Pyrrolidines.
@en
Regio- and Diastereoselective ...... ,5-Disubstituted Pyrrolidines.
@nl
P2093
P2860
P356
P1476
Regio- and Diastereoselective ...... ,5-Disubstituted Pyrrolidines.
@en
P2093
Debasis Koley
Subhra Kanti Roy
Surajit Haldar
P2860
P304
15290-15298
P356
10.1002/CHEM.201502297
P407
P577
2015-09-07T00:00:00Z