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Lactosamine from lactulose via the Heyns rearrangement : a practical protocol

Shan, Yulong (author)
Univ Bangor, Sch Chem, Bangor LL57 2UW, Gwynedd, Wales.
Oulaidi, Farah (author)
Univ Bangor, Sch Chem, Bangor LL57 2UW, Gwynedd, Wales.
Lahmann, Martina (author)
Univ Bangor, Sch Chem, Bangor LL57 2UW, Gwynedd, Wales.
Univ Bangor, Sch Chem, Bangor LL57 2UW, Gwynedd, Wales (creator_code:org_t)
PERGAMON-ELSEVIER SCIENCE LTD, 2013
2013
English.
In: Tetrahedron Letters. - : PERGAMON-ELSEVIER SCIENCE LTD. - 0040-4039 .- 1359-8562. ; 54:30, s. 3960-3961
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The Heyns rearrangement is possibly one of the oldest, easiest and most economic ways to synthesise 2-deoxy-2-amino sugars. Initially reported yields were disappointingly low, but in the late 90s Wrodnigg and Stutz discovered modified reaction conditions that gave substantially increased yields, making the reaction viable on preparative scale. Requiring larger amounts of N-acetyl lactosamine, we utilised the reported reaction conditions and found that additional modifications, especially in the work-up procedure-for example employing rapid filtration of crude diethyl ether precipitates, were necessary to make this approach robust in the research laboratory environment.

Subject headings

NATURVETENSKAP  -- Kemi -- Organisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Organic Chemistry (hsv//eng)

Keyword

Heyns rearrangement
N-Acetyllactosamine lactulose
2-Deoxy-2-amino sugar

Publication and Content Type

ref (subject category)
art (subject category)

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Shan, Yulong
Oulaidi, Farah
Lahmann, Martina
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NATURAL SCIENCES
NATURAL SCIENCES
and Chemical Science ...
and Organic Chemistr ...
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Tetrahedron Lett ...
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Royal Institute of Technology

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