Enantioselective Diels-Alder-lactamization organocascades employing a furan-based diene-Reference-Cited by-同舟云学术

Enantioselective Diels-Alder-lactamization organocascades employing a furan-based diene

Published:2017 Issue:15 Volume:15 Page:3179-3183
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Abbasov Mikail E.¹²³⁴,Hudson Brandi M.⁵⁶⁷⁸⁴^ORCID,Kong Weixu¹²³⁴,Tantillo Dean J.⁵⁶⁷⁸⁴,Romo Daniel¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry and Biochemistry

2. Baylor University

3. Waco

4. USA

5. Department of Chemistry

6. University of California-Davis

7. Davis

8. 95616

Abstract

α,β-Unsaturated acylammonium salts are useful dienophiles enabling highly enantioselective and stereodivergent Diels-Alder-initiated organocascades with furan-based dienes.

Funder

American Chemical Society Petroleum Research Fund

Division of Chemistry

National Institute of General Medical Sciences

Welch Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/OB/C6OB02738E

Reference40 articles.

1. Unusual stability of N-methylmaleimide cycloadducts: characterization of isobenzofuran retro-Diels-Alder reactions

2. Irreversibleendo-Selective Diels-Alder Reactions of Substituted Alkoxyfurans: A General Synthesis ofendo-Cantharimides

3. The N,O-bridged sesquinorbornadienes: a testing ground for establishing the superiority of N-Z pyrrole over furan as a dienofuge in retro-Diels–Alder reactions

4. Skeletal Wagner–Meerwein rearrangement of perhydro-3a,6;4,5-diepoxyisoindoles

5. Study of the Diels–Alder and retro-Diels–Alder reaction between furan derivatives and maleimide for the creation of new materials

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