Microwave-Based Reaction Screening: Tandem Retro-Diels–Alder/Diels–Alder Cycloadditions ofo-Quinol Dimers-Reference-Cited by-同舟云学术

Microwave-Based Reaction Screening: Tandem Retro-Diels–Alder/Diels–Alder Cycloadditions ofo-Quinol Dimers

Published:2011-10-07 Issue:21 Volume:76 Page:8944-8954
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Dong Suwei¹,Cahill Katharine J.²,Kang Moon-Il³,Colburn Nancy H.³,Henrich Curtis J.³,Wilson Jennifer A.³,Beutler John A.³,Johnson Richard P.²,Porco John A.¹

Affiliation:

1. Department of Chemistry and Center for Chemical Methodology and Library Development (CMLD-BU), Boston University, Boston, Massachusetts 02215, United States

2. Department of Chemistry, University of New Hampshire, Durham, New Hampshire 03824, United States

3. Laboratory of Cancer Prevention and Molecular Targets Laboratory, Center for Cancer Research, NCI-Frederick, Frederick, Maryland 21702, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo201658y

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2. Synthesis of tricyclo[7.2.2.02,8]tridecanes and photoreaction in the excited singlet state: A novel entry to the DCB carbon framework of phorbol

3. Enantioselective Synthesis of (+)‐Chamaecypanone C: A Novel Microtubule Inhibitor

4. Masked o-Benzoquinones in Organic Synthesis

5. Domino retro Diels–Alder/Diels–Alder reaction: an efficient protocol for the synthesis of highly functionalized bicyclo[2.2.2]octenones and bicyclo[2.2.2]octadienones

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