Acceleration of acetal hydrolysis by remote alkoxy groups: evidence for electrostatic effects on the formation of oxocarbenium ions.
about
Participation of alkoxy groups in reactions of acetals: violation of the reactivity/selectivity principle in a Curtin-Hammett kinetic scenario.Stereoelectronic Model To Explain Highly Stereoselective Reactions of Seven-Membered-Ring Oxocarbenium-Ion IntermediatesDetermination of the Influence of Side-Chain Conformation on Glycosylation Selectivity using Conformationally Restricted Donors.Absence of Stereodirecting Participation by 2-O-Alkoxycarbonylmethyl Ethers in 4,6-O-Benzylidene-Directed Mannosylation.
P2860
Acceleration of acetal hydrolysis by remote alkoxy groups: evidence for electrostatic effects on the formation of oxocarbenium ions.
description
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2015年の論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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name
Acceleration of acetal hydroly ...... ormation of oxocarbenium ions.
@ast
Acceleration of acetal hydroly ...... ormation of oxocarbenium ions.
@en
type
label
Acceleration of acetal hydroly ...... ormation of oxocarbenium ions.
@ast
Acceleration of acetal hydroly ...... ormation of oxocarbenium ions.
@en
prefLabel
Acceleration of acetal hydroly ...... ormation of oxocarbenium ions.
@ast
Acceleration of acetal hydroly ...... ormation of oxocarbenium ions.
@en
P2093
P2860
P356
P1476
Acceleration of acetal hydroly ...... ormation of oxocarbenium ions.
@en
P2093
Angie Garcia
Douglas A L Otte
Jillian R Sanzone
K A Woerpel
Walter A Salamant
P2860
P304
P356
10.1002/ANIE.201410043
P407
P577
2015-01-22T00:00:00Z