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Diastereoselective Aldol Additions to α-Amino-β-Silyloxy Aldehydes. Divergent Synthesis of Aminodiols

Restorp, Per (author)
KTH,Organisk kemi
Somfai, Peter (author)
KTH,Organisk kemi
 (creator_code:org_t)
2005-02-02
2005
English.
In: Organic Letters. - : American Chemical Society (ACS). - 1523-7060 .- 1523-7052. ; 7:5, s. 893-895
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • A divergent protocol for substrate-controlled diastereoselective synthesis of aminodiols has been developed using nucleophilic Mukaiyama aldol additions to alpha-amino-beta-silyloxy aldehydes. The merged stereochemical impact on the diastereoselectivity of the polar alpha- and beta-substituents is highlighted.

Subject headings

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

Keyword

MERGED STEREOCHEMICAL IMPACT
1
3-ASYMMETRIC INDUCTION
ALKOXY ALDEHYDES
LEWIS-ACIDS
ALLYLTRIMETHYLSILANE
Organic chemistry
Organisk kemi

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ref (subject category)
art (subject category)

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By the author/editor
Restorp, Per
Somfai, Peter
About the subject
NATURAL SCIENCES
NATURAL SCIENCES
and Chemical Science ...
and Organic Chemistr ...
Articles in the publication
Organic Letters
By the university
Royal Institute of Technology

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