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research article

Synthetic Studies toward Ecteinascidin 743

Chen, Xiaochuan
•
Chen, Jinchun
•
De Paolis, Michael
Show more
2005
The Journal of Organic Chemistry

An efficient synthesis of a fully functionalized tetracyclic fragment (A-B-C-H) I of ecteinascidin 743, contg. a 1,4-bridged 10-membered lactone, is reported. The synthesis is highly convergent and has been carried out on a multigram scale featuring the following key steps: union of two fragments II and III via an oxazolidine intermediate; and acid-promoted macrocyclization via formation of a carbon-sulfur bond with concomitant formation of the 10-membered ring. Although compd. I was responsive to the intramol. Pictet-Spengler reaction, a destructive ring opening of the 1,4-bridged lactone also occurred, leading to the formation of pentacyclic compd. IV. In the course of this study, it was discovered that a combination of a mild Lewis acid and a mild Bronsted acid constituted excellent reagents for performing the Pictet-Spengler reaction of a highly acid-sensitive substrate. [on SciFinder (R)]

  • Details
  • Metrics
Type
research article
DOI
10.1021/jo050408k
Author(s)
Chen, Xiaochuan
Chen, Jinchun
De Paolis, Michael
Zhu, Jieping  
Date Issued

2005

Published in
The Journal of Organic Chemistry
Volume

70

Issue

11

Start page

4397

End page

4408

Subjects

Cyclocondensation reaction (Pictet-Spengler; synthetic studies toward ecteinascidin 743); Amination (Strecker; synthetic studies toward ecteinascidin 743); Macrocyclization (acid-promoted macrocyclization; synthetic studies toward ecteinascidin 743); Crystal structure; Molecular structure (of a substituted phenolic intermediate in synthetic studies toward ecteinascidin 743); Asymmetric synthesis and induction; Condensation reaction (synthetic studies toward ecteinascidin 743)

•

asym synthesis ecteinascidin 743 tetracycle condensation Strecker Pictet Spengler; crystal mol structure phenolic intermediate

Note

CAN 143:60125

31-6

Alkaloids

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

Journal

written in English.

654644-01-6P Role: PRP (Properties), SPN (Synthetic preparation), PREP (Preparation) (crystal structure; synthetic studies toward ecteinascidin 743); 200132-54-3 Role: CAT (Catalyst use), USES (Uses) (synthetic studies toward ecteinascidin 743); 108-88-3 (Toluene); 920-66-1 Role: NUU (Other use, unclassified), USES (Uses) (synthetic studies toward ecteinascidin 743); 114899-77-3P (Ecteinascidin 743) Role: PNU (Preparation, unclassified), PREP (Preparation) (synthetic studies toward ecteinascidin 743); 106-95-6 (Allyl bromide); 488-17-5; 533-31-3 (1,3-Benzodioxol-5-ol); 924-44-7 (Ethyl glyoxylate); 2799-07-7; 3966-32-3; 26164-26-1; 81477-94-3; 95715-87-0; 96845-11-3 Role: RCT (Reactant), RACT (Reactant or reagent) (synthetic studies toward ecteinascidin 743); 111726-43-3P; 187040-02-4P; 187040-03-5P; 654643-96-6P; 654643-97-7P; 654643-98-8P; 654643-99-9P; 654644-00-5P; 654644-02-7P; 654644-03-8P; 654644-04-9P; 686776-20-5P; 686776-21-6P; 686776-22-7P; 686776-23-8P; 686776-24-9P; 686776-25-0P; 686776-28-3P; 686776-29-4P; 854021-71-9P; 854021-83-3P; 854021-99-1P; 854022-02-9P; 854022-04-1P; 854022-09-6P; 854022-14-3P; 854022-23-4P; 854022-25-6P; 854022-31-4P; 854022-33-6P; 854022-35-8P; 854022-39-2P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (synthetic studies toward ecteinascidin 743); 7447-41-8 (Lithium chloride) Role: RGT (Reagent), RACT (Reactant or reagent) (synthetic studies toward ecteinascidin 743); 654643-95-5P; 854021-95-7P; 854021-97-9P; 854022-01-8P; 854022-06-3P; 854022-12-1P; 854022-29-0P; 854022-37-0P Role: SPN (Synthetic preparation), PREP (Preparation) (synthetic studies toward ecteinascidin 743)

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/20.500.14299/58473
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