Oxidative intramolecular [4 + 2]cycloaddition of silylene-protected 2-pyridone derivatives—a short and efficient synthesis of the DEF-ring of fredericamycin A-Reference-Cited by-同舟云学术

Oxidative intramolecular [4 + 2]cycloaddition of silylene-protected 2-pyridone derivatives—a short and efficient synthesis of the DEF-ring of fredericamycin A

Published:1994 Issue:6 Volume: Page:701-702
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Kita Yasuyuki,Ueno Hiroshi,Kitagaki Shinji,Kobayashi Kyoko,Lio Kiyosei,Akai Shuji

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1994/C3/C39940000701

Reference23 articles.

1. Antitumor anthracyclines: Recent developments

2. Anthracyclinone syntheses using strong base induced cycloaddition of homophthalic anhydrides and related compounds

3. Synthesis of anthracycline antibiotics. Cycloaddition reaction of homophthalic anhydrides and their related compounds.

4. Strong base-induced intramolecular cycloaddition of homophthalic anhydrides: an efficient synthesis of polycyclic peri-hydroxy aromatic compounds

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