Borrowing hydrogen methodology for the conversion of alcohols into N-protected primary amines and in situ deprotection

Gareth W Lamb; Andrew J A Watson; K E Jolley; A C Maxwell; Jonathan MJ Williams

doi:10.1016/j.tetlet.2009.02.129

Borrowing hydrogen methodology for the conversion of alcohols into N-protected primary amines and in situ deprotection

Gareth W Lamb
, Andrew J A Watson
, K E Jolley
, A C Maxwell
, Jonathan MJ Williams

Research output: Contribution to journal › Article › peer-review

60 Citations (SciVal)

Abstract

Alcohols have been converted into a range of protected amines including sulfonamides and N-alkylbenzylamine derivatives. Representative examples of deprotection to afford primary amines are also provided.

Original language	English
Pages (from-to)	3374-3377
Number of pages	4
Journal	Tetrahedron Letters
Volume	50
Issue number	26
DOIs	https://doi.org/10.1016/j.tetlet.2009.02.129
Publication status	Published - 2009

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10.1016/j.tetlet.2009.02.129

Cite this

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title = "Borrowing hydrogen methodology for the conversion of alcohols into N-protected primary amines and in situ deprotection",

abstract = "Alcohols have been converted into a range of protected amines including sulfonamides and N-alkylbenzylamine derivatives. Representative examples of deprotection to afford primary amines are also provided.",

author = "Lamb, \{Gareth W\} and Watson, \{Andrew J A\} and Jolley, \{K E\} and Maxwell, \{A C\} and Williams, \{Jonathan MJ\}",

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T1 - Borrowing hydrogen methodology for the conversion of alcohols into N-protected primary amines and in situ deprotection

AU - Lamb, Gareth W

AU - Watson, Andrew J A

AU - Jolley, K E

AU - Maxwell, A C

AU - Williams, Jonathan MJ

PY - 2009

Y1 - 2009

N2 - Alcohols have been converted into a range of protected amines including sulfonamides and N-alkylbenzylamine derivatives. Representative examples of deprotection to afford primary amines are also provided.

AB - Alcohols have been converted into a range of protected amines including sulfonamides and N-alkylbenzylamine derivatives. Representative examples of deprotection to afford primary amines are also provided.

UR - https://www.scopus.com/pages/publications/65549151848

UR - http://dx.doi.org/10.1016/j.tetlet.2009.02.129

U2 - 10.1016/j.tetlet.2009.02.129

DO - 10.1016/j.tetlet.2009.02.129

M3 - Article

SN - 0040-4039

VL - 50

SP - 3374

EP - 3377

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 26

ER -

Borrowing hydrogen methodology for the conversion of alcohols into N-protected primary amines and in situ deprotection

Abstract

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TERTIARY AMINES FROM ALCOHOLS WITHOUT OXIDANTS, REDUCTANTS O R ALKY HALIDES

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Borrowing hydrogen methodology for the conversion of alcohols into N-protected primary amines and in situ deprotection

Abstract

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TERTIARY AMINES FROM ALCOHOLS WITHOUT OXIDANTS, REDUCTANTS O R ALKY HALIDES

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