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N-Tritylprolinal: An Efficient Building Block for theStereoselective Synthesis of Proline-Derived Amino Alcohols
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http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_25/w
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Title
N-Tritylprolinal: An Efficient Building Block for theStereoselective Synthesis of Proline-Derived Amino Alcohols
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http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_25/101021jo034976g/m/web
http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_25/101021jo034976g/m/print
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http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_25/101021jo034976g/authorship/3
http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_25/101021jo034976g/authorship/2
http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_25/101021jo034976g/authorship/1
Author
Bejjani Joseph
Audouin Max
Chemla Fabrice
Abstract
N-Tritylprolinal (prepared in four steps from l-proline) shows a very high Felkin diastereoselectivityin its reaction with various nucleophiles, leading to a straightforward and highly stereoselectiveaccess to syn-proline-derived amino alcohols.
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The Journal of Organic Chemistry
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