A Stereoselective and Atom-Efficient Approach to Multifunctionalized Five- and Six-Membered Rings via a Novel Michael-Initiated Intramolecular Diels−Alder Furan Reaction-Reference-Cited by-同舟云学术

A Stereoselective and Atom-Efficient Approach to Multifunctionalized Five- and Six-Membered Rings via a Novel Michael-Initiated Intramolecular Diels−Alder Furan Reaction

Published:2005-02-19 Issue:6 Volume:70 Page:2235-2243
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Namboothiri Irishi N. N.¹,Ganesh Madhu¹,Mobin Shaikh M.¹,Cojocaru Miriam¹

Affiliation:

1. Department of Chemistry and National Single-Crystal X-ray Diffraction Facility, Indian Institute of Technology, Bombay, Mumbai 400 076, India, and Department of Chemistry, Bar-Ilan University, Ramat Gan 52900, Israel

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo048262x

Reference29 articles.

1. Five-membered heteroaromatic rings as intermediates in organic synthesis

2. Aspects of the intramolecular diels-alder reaction of a furan diene (IMDAF) leading to the formation of 1,4-epoxydecalin systems

3. Total Synthesis Of Biologically Intriguing Drimane-Type Sesquiterpenoids Via Intramolecular Diels–Alder Approaches

4. Rh(I)-Catalyzed Ring Opening of an IMDAF-Derived Oxabicyclo Cycloadduct as the Key Step in the Synthesis of (±)-epi-Zephyranthine

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