Search: onr:"swepub:oai:DiVA.org:kth-6620" >
Diastereoselective ...
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
- Related links:
-
https://urn.kb.se/re...
-
show more...
-
https://doi.org/10.1...
-
show less...
Abstract
Subject headings
Close
- 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
Publication and Content Type
- ref (subject category)
- art (subject category)
Find in a library
To the university's database