EFFECT OF CONFORMATION AND STEREOCHEMISTRY IN SUBSTITUTION REACTIONS OF FUSED CHLOROCYCLOBUTANONES: OXYALLYL CATION INTERMEDIATES

DOI: 10.1016/S0040-4039(00)86385-6

Source and publish data:

Tetrahedron Letters p. 1135 - 1138 (1983)

Update date:2022-09-26

Topics:

Authors:

Hassner, Alfred

Dillon, John L.

Krepski, Larry R.

Onan, Kay D.

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Article abstract of DOI:10.1016/S0040-4039(00)86385-6

Fused α-acyloxycyclobutanones, whose conformation and stereochemistry have been unambiguosly established by X-ray analysis, undergo an unususal displacement with methoxide as nucleophile to produce α-methoxycyclobutanones.The success of this reaction, whi

Full text of DOI:10.1016/S0040-4039(00)86385-6

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Article Doi

EFFECT OF CONFORMATION AND STEREOCHEMISTRY IN SUBSTITUTION REACTIONS OF FUSED CHLOROCYCLOBUTANONES: OXYALLYL CATION INTERMEDIATES

DOI: 10.1016/S0040-4039(00)86385-6

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)86385-6

Full text of DOI:10.1016/S0040-4039(00)86385-6

Products guided by the article

R&D Labs maybe for 86477-35-2

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Synthesis of fluorinated derivatives of 4 hydroxycoumarin and chromone

A Simple, Unambiguous Synthesis of 2-Amino-4-oxo- and -4-thioxo-3,4-dihydropyrimidine-5-carbonitriles

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An efficient method for the synthesis of nitropiperidones

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