The 9-Phenyl-9-fluorenyl Group for Nitrogen Protection in Enantiospecific Synthesis-Reference-Cited by-同舟云学术

The 9-Phenyl-9-fluorenyl Group for Nitrogen Protection in Enantiospecific Synthesis

Published:2010-09-17 Issue:9 Volume:15 Page:6512-6547
ISSN:1420-3049
Container-title:Molecules
language:en
Short-container-title:Molecules

Author:

Karppanen Essi J.,Koskinen Ari M. P.

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

Link

http://www.mdpi.com/1420-3049/15/9/6512/pdf

Reference55 articles.

1. The enantio- and diastereoselective synthesis of the first phospho-statine derivative

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3. Synthesis of optically pure pipecolates from L-asparagine. Application to the total synthesis of (+)-apovincamine through amino acid decarbonylation and iminium ion cyclization

4. Enantiomerically pure dimethyl (2S)-N-(9-phenylfluoren-9-yl)-3,4-didehydroglutamate as chiral educt. Chirospecific synthesis of (+)-5-O-carbamoylpolyoxamic acid and 3-alkylglutamates

5. Configurational stability of N-protected .alpha.-amino aldehydes

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