Reductive deprotection of allyl, benzyl and sulfonyl substituted alcohols, amines and amides using a naphthalene-catalysed lithiation

DOI: 10.1016/S0040-4020(97)00920-4

Source and publish data:

Tetrahedron p. 14355 - 14368 (1997)

Update date:2022-08-03

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Authors:

Alonso, Emma

Ramon, Diego J.

Yus, Miguel

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Article abstract of DOI:10.1016/S0040-4020(97)00920-4

The reaction of different protected alcohols, amines and amides with lithium and a catalytic amount of naphthalene (4 mol %) in THF at low temperature leads to their deprotection under very mild reaction conditions, the process being in many cases chemoselective.

Full text of DOI:10.1016/S0040-4020(97)00920-4

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Article Doi

Reductive deprotection of allyl, benzyl and sulfonyl substituted alcohols, amines and amides using a naphthalene-catalysed lithiation

DOI: 10.1016/S0040-4020(97)00920-4

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4020(97)00920-4

Full text of DOI:10.1016/S0040-4020(97)00920-4

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R&D Labs maybe for 197958-51-3

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3-Aminomethyl-5-hydroxybenzo[b]thiophenes.

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Facile activation of carbon-fluorine bonds in saturated fluoroalkyl ligands by coordinated water in fluoroalkyl aqua complexes of rhodium [6]

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