Stereoselective Lewis acid mediated (3+2) cycloadditions of N-H- and N-sulfonylaziridines with heterocumulenes.
about
Lewis Acid-Catalyzed Intramolecular [3+2] Cross-Cycloaddition of Aziridine 2,2-Diesters with Conjugated Dienes for Construction of Aza-[n.2.1] Skeletons.Breaking aziridines to construct morpholines with a gold(i)-catalyzed tandem ring-opening and cycloisomerization reaction.Alkene functionalization for the stereospecific synthesis of substituted aziridines by visible-light photoredox catalysis.Synthetic route to chiral indolines via Cu(OAc)2-catalyzed ring-opening/C(sp2)-H activation of activated aziridines.
P2860
Stereoselective Lewis acid mediated (3+2) cycloadditions of N-H- and N-sulfonylaziridines with heterocumulenes.
description
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name
Stereoselective Lewis acid med ...... iridines with heterocumulenes.
@ast
Stereoselective Lewis acid med ...... iridines with heterocumulenes.
@en
type
label
Stereoselective Lewis acid med ...... iridines with heterocumulenes.
@ast
Stereoselective Lewis acid med ...... iridines with heterocumulenes.
@en
prefLabel
Stereoselective Lewis acid med ...... iridines with heterocumulenes.
@ast
Stereoselective Lewis acid med ...... iridines with heterocumulenes.
@en
P2860
P356
P1476
Stereoselective Lewis acid med ...... iridines with heterocumulenes.
@en
P2093
Brian M Stoltz
Nicholas R O'Connor
P2860
P304
P356
10.1002/CHEM.201303699
P407
P577
2014-03-06T00:00:00Z