3-Amino-1-hydroxyacetone

Nisar Ullah; Clara Nanfe Fali; Ian D. Spenser

doi:10.1139/v04-010

3-Amino-1-hydroxyacetone

Nisar Ullah
, Clara Nanfe Fali
, Ian D. Spenser^*

^*Corresponding author for this work

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

5 Scopus citations

Abstract

3-Amino-1-hydroxypropan-2-one (3-amino-1-hydroxyacetone) was prepared in an overall yield of 52% in 6 steps starting with N-phthaloylglycine. This synthesis is readily adaptable for the preparation of bond-labeled samples, i.e., samples that are labeled intramolecularly at contiguous sites.

Original language	English
Pages (from-to)	579-582
Number of pages	4
Journal	Canadian Journal of Chemistry
Volume	82
Issue number	5
DOIs	https://doi.org/10.1139/v04-010
State	Published - May 2004
Externally published	Yes

Keywords

3-amino-1-hydroxyacetone
3-amino-1-hydroxypropan-2-one

ASJC Scopus subject areas

Catalysis
General Chemistry
Organic Chemistry

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10.1139/v04-010

Cite this

@article{796c18c61cc5467184532f0582768cf4,

title = "3-Amino-1-hydroxyacetone",

abstract = "3-Amino-1-hydroxypropan-2-one (3-amino-1-hydroxyacetone) was prepared in an overall yield of 52\% in 6 steps starting with N-phthaloylglycine. This synthesis is readily adaptable for the preparation of bond-labeled samples, i.e., samples that are labeled intramolecularly at contiguous sites.",

keywords = "3-amino-1-hydroxyacetone, 3-amino-1-hydroxypropan-2-one",

author = "Nisar Ullah and Fali, \{Clara Nanfe\} and Spenser, \{Ian D.\}",

year = "2004",

month = may,

doi = "10.1139/v04-010",

language = "English",

volume = "82",

pages = "579--582",

journal = "Canadian Journal of Chemistry",

issn = "0008-4042",

number = "5",

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TY - JOUR

T1 - 3-Amino-1-hydroxyacetone

AU - Ullah, Nisar

AU - Fali, Clara Nanfe

AU - Spenser, Ian D.

PY - 2004/5

Y1 - 2004/5

N2 - 3-Amino-1-hydroxypropan-2-one (3-amino-1-hydroxyacetone) was prepared in an overall yield of 52% in 6 steps starting with N-phthaloylglycine. This synthesis is readily adaptable for the preparation of bond-labeled samples, i.e., samples that are labeled intramolecularly at contiguous sites.

AB - 3-Amino-1-hydroxypropan-2-one (3-amino-1-hydroxyacetone) was prepared in an overall yield of 52% in 6 steps starting with N-phthaloylglycine. This synthesis is readily adaptable for the preparation of bond-labeled samples, i.e., samples that are labeled intramolecularly at contiguous sites.

KW - 3-amino-1-hydroxyacetone

KW - 3-amino-1-hydroxypropan-2-one

UR - https://www.scopus.com/pages/publications/3042709839

U2 - 10.1139/v04-010

DO - 10.1139/v04-010

M3 - Article

AN - SCOPUS:3042709839

SN - 0008-4042

VL - 82

SP - 579

EP - 582

JO - Canadian Journal of Chemistry

JF - Canadian Journal of Chemistry

IS - 5

ER -

3-Amino-1-hydroxyacetone

Abstract

Keywords

ASJC Scopus subject areas

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