Ring fission of chiral cyclic acetals plus intramolecular [4 + 2] cycloaddition: a sequential access to medium-size lactones. Application to the synthesis of carbasugars-Reference-Cited by-同舟云学术

Ring fission of chiral cyclic acetals plus intramolecular [4 + 2] cycloaddition: a sequential access to medium-size lactones. Application to the synthesis of carbasugars

Published:2005 Issue:7 Volume:3 Page:1308-1318
ISSN:1477-0520
Container-title:Org. Biomol. Chem.
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Lemiègre Loïc,Stevens Richard L.,Combret Jean-Claude,Maddaluno Jacques

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2005/OB/B419381D

Reference70 articles.

1. Stereochemical aspects of the intramolecular Diels–Alder reaction

2. Harvesting Diels and Alder's Garden: Synthetic Investigations of Intramolecular [4 + 2] Cycloadditions

3. gem-Dialkyl effect in the intramolecular Diels-Alder reaction of 2-furfuryl methyl fumarates: the reactive rotamer effect, the enthalpic basis for acceleration, and evidence for a polar transition state

4. Substituent Effects in the Intramolecular Diels−Alder Reaction of 6-Furylhexenoates

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