An n→π* interaction reduces the electrophilicity of the acceptor carbonyl group.

An n→π* interaction reduces the electrophilicity of the acceptor carbonyl group.

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http://www.wikidata.org/entity/Q41876053
Electronic and Steric Optimization of Fluorogenic Probes for Biomolecular ImagingA benzotriazole-mediated route to protected marine-derived hetero-2,5-diketopiperazines containing proline.Tailored Synthesis of 162-Residue S-Monoglycosylated GM2-Activator Protein (GM2AP) Analogues that Allows Facile Access to a Protein Library.n→π* Interactions Are Competitive with Hydrogen Bonds.OGlcNAcylation and phosphorylation have opposing structural effects in tau: phosphothreonine induces particular conformational order.The n→π* Interactionn→π* interactions engender chirality in carbonyl groupsStereodivergent, Diels-Alder-initiated organocascades employing α,β-unsaturated acylammonium salts: scope, mechanism, and application.A key n→π* Interaction in N-acyl homoserine lactones.Examination of native chemical ligation using peptidyl prolyl thioesters.
P2860

An n→π* interaction reduces the electrophilicity of the acceptor carbonyl group.

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http://www.wikidata.org/entity/Q41876053
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
An n→π* interaction reduces the electrophilicity of the acceptor carbonyl group.
@en
type
label
An n→π* interaction reduces the electrophilicity of the acceptor carbonyl group.
@en
prefLabel
An n→π* interaction reduces the electrophilicity of the acceptor carbonyl group.
@en
P1433
P1476
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P698
P932
P356
P1433
P1476
An n→π* interaction reduces the electrophilicity of the acceptor carbonyl group.
@en
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P698
P932