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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2014/08/27 06:30:02」(JST)

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Neighbouring group participation (NGP) or Anchimeric assistance in organic chemistry has been defined by IUPAC as the interaction of a reaction centre with a lone pair of electrons in an atom or the electrons present in a sigma bond or pi bond ^[1]. When NGP is in operation it is normal for the reaction rate to be increased. It is also possible for the stereochemistry of the reaction to be abnormal (or unexpected) when compared with a normal reaction. While it is possible for neighbouring groups to influence many reactions in organic chemistry (For instance the reaction of a diene such as cyclohex-1,3-diene with maleic anhydride normally gives the endo isomer because of a secondary effect {overlap of the carbonyl group π orbitals with the transition state in the Diels-Alder reaction}) this page is limited to neighbouring group effects seen with carbocations and S_N2 reactions.

NGP by heteroatom lone pairs

A classic example of NGP is the reaction of a sulfur or nitrogen mustard with a nucleophile, the rate of reaction is much higher for the sulfur mustard and a nucleophile than it would be for a primary alkyl chloride without a heteroatom.

In sugar chemistry anchimeric assistance is an example of NGP.

NGP by an alkene

The π orbitals of an alkene can stabilize a transition state by helping to delocalize the positive charge of the carbocation. For instance the unsaturated tosylate will react more quickly (10¹¹ times faster for aqueous solvolysis) with a nucleophile than the saturated tosylate.

The carbocationic intermediate will be stabilized by resonance where the positive charge is spread over several atoms, in the diagram below this is shown.

Here is a different view of the same intermediates.

Even if the alkene is more remote from the reacting center the alkene can still act in this way. For instance in the following alkyl benzenesulfonate the alkene is able to delocalise the carbocation.

Also the increase in the rate of the SN2 reaction of allyl bromide with a nucleophile compared with the reaction of n-propyl bromide is because the orbitals of the π bond overlap with those of the transition state. In the allyl system the alkene orbitals overlap with the orbitals of a S_N2 transition state.

NGP by a cyclopropane, cyclobutane or a homoallyl group

If Cyclopropylmethyl chloride is reacted with ethanol and water then a mixture of 48% cyclopropylmethyl alcohol, 47% cyclobutanol and 5% homoallyl alcohol (but-3-enol) is obtained. This is because the carbocationic intermidate is delocalised onto many different carbons through a reversible ring opening.

NGP by an aromatic ring

In the case of a benzyl halide the reactivity is higher for the because the S_N2 transition state enjoys a similar overlap effect to that in the allyl system.

An aromatic ring can assist in the formation of a carbocationic intermediate called a phenonium ion by delocalising the positive charge.

When the following tosylate reacts with acetic acid in solvolysis then rather than a simple S_N2 reaction forming B, a 48:48:4 mixture of A, B and (C+D) was obtained ^[2] ^[3].

The mechanism which forms A and B is shown below.

External links

A PhD thesis written on this subject is at [4].
IUPAC definition

References

^ Advanced organic chemistry, page 314, Jerry March (4th Ed), Wiley-Interscience.
^ Studies in Stereochemistry. I. The Stereospecific Wagner-Meerwein Rearrangement of the Isomers of 3-Phenyl-2-butanol Donald J. Cram J. Am. Chem. Soc.; 1949; 71(12); 3863-3870. Abstract
^ Studies in Stereochemistry. V. Phenonium Sulfonate Ion-pairs as Intermediates in the Intramolecular Rearrangements and Solvolysis Reactions that Occur in the 3-Phenyl-2-butanol System Donald J. Cram J. Am. Chem. Soc.; 1952; 74(9); 2129-2137 Abstract.

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English Journal

Thia-, aza-, and selena[3.3.1]bicyclononane dichlorides: rates vs internal nucleophile in anchimeric assistance.

Accurso AA, Cho SH, Amin A, Potapov VA, Amosova SV, Finn MG.SourceDepartment of Chemistry and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, La Jolla, California 92037, United States.
The Journal of organic chemistry.J Org Chem.2011 Jun 3;76(11):4392-5. Epub 2011 May 5.
Sulfur-, selenium-, and nitrogen-containing compounds bearing leaving groups in the β-position undergo facile substitution chemistry enabled by anchimeric assistance. Here we provide direct comparisons between such systems in the rigid bicyclo[3.3.1]nonane framework easily derived from 1,5-cyclooct
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Cationic ester-containing gemini surfactants: physical-chemical properties.

Tehrani-Bagha AR, Holmberg K.SourceDepartment of Chemical and Biological Engineering, Chalmers University of Technology, SE-412 96 Goteborg, Sweden.
Langmuir : the ACS journal of surfaces and colloids.Langmuir.2010 Jun 15;26(12):9276-82.
Three ester-containing cationic gemini surfactants, two with decanoyl chains and either a three-carbon or a six-carbon spacer unit and one with dodecanoyl chains and a three-carbon spacer, were synthesized and evaluated. A corresponding monomeric cationic ester surfactant was used for comparison. Th
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