Repository logo

Infoscience

  • English
  • French
Log In
Logo EPFL, École polytechnique fédérale de Lausanne

Infoscience

  • English
  • French
Log In
  1. Home
  2. Academic and Research Output
  3. Journal articles
  4. A short enantioselective synthesis of protected L-3-hydroxy-4-methoxy-5-methyl phenylalanine and its corresponding aldehyde - a common subunit of ecteinascidin-743, safracin and congeners
 
research article

A short enantioselective synthesis of protected L-3-hydroxy-4-methoxy-5-methyl phenylalanine and its corresponding aldehyde - a common subunit of ecteinascidin-743, safracin and congeners

De Paolis, Michael
•
Chen, Xiaochuan
•
Zhu, Jieping  
2004
Synlett

An asym. synthesis of appropriately protected L-3-hydroxy-4-methoxy-5-Me phenylalanine from 3-methylcatechol is described featuring a key enantioselective alkylation step. [on SciFinder (R)]

  • Details
  • Metrics
Type
research article
DOI
10.1055/s-2004-817763
Author(s)
De Paolis, Michael
•
Chen, Xiaochuan
•
Zhu, Jieping  
Date Issued

2004

Published in
Synlett
Issue

4

Start page

729

End page

731

Subjects

Asymmetric synthesis and induction (asym. prepn. of a phenylalanine deriv. and its corresponding aldehyde using enantioselective alkylation as a key step); Alkylation (stereoselective; asym. prepn. of a phenylalanine deriv. and its corresponding aldehyde using enantioselective alkylation as a key step)

•

ecteinascidin component phenylalanine deriv prepn enantioselective alkylation

Note

CAN 140:391464

34-2

Amino Acids, Peptides, and Proteins

Institut de Chimie des Substances Naturelles, CNRS,Gif-sur-Yvette,Fr.

Journal

written in English.

200132-54-3 Role: CAT (Catalyst use), USES (Uses) (asym. prepn. of a phenylalanine deriv. and its corresponding aldehyde using enantioselective alkylation as a key step); 488-17-5; 7764-95-6; 81477-94-3 Role: RCT (Reactant), RACT (Reactant or reagent) (asym. prepn. of a phenylalanine deriv. and its corresponding aldehyde using enantioselective alkylation as a key step); 244126-22-5P; 686776-20-5P; 686776-22-7P; 686776-23-8P; 686776-24-9P; 686776-25-0P; 686776-27-2P; 686776-28-3P; 686776-29-4P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (asym. prepn. of a phenylalanine deriv. and its corresponding aldehyde using enantioselective alkylation as a key step); 686776-21-6P; 686776-26-1P Role: SPN (Synthetic preparation), PREP (Preparation) (asym. prepn. of a phenylalanine deriv. and its corresponding aldehyde using enantioselective alkylation as a key step); 87578-99-2 (Safracin B); 114899-77-3 (Ecteinascidin-743) Role: MSC (Miscellaneous) (asym. prepn. of a phenylalanine deriv. and its corresponding aldehyde, key components of ecteinascidin-743 and safracin-B); 686776-30-7P; 686776-31-8P Role: SPN (Synthetic preparation), PREP (Preparation) (stereochem. detn. of)

Editorial or Peer reviewed

REVIEWED

Written at

OTHER

EPFL units
LSPN  
Available on Infoscience
November 25, 2010
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/58480
Logo EPFL, École polytechnique fédérale de Lausanne
  • Contact
  • infoscience@epfl.ch

  • Follow us on Facebook
  • Follow us on Instagram
  • Follow us on LinkedIn
  • Follow us on X
  • Follow us on Youtube
AccessibilityLegal noticePrivacy policyCookie settingsEnd User AgreementGet helpFeedback

Infoscience is a service managed and provided by the Library and IT Services of EPFL. © EPFL, tous droits réservés