Sequential 1,2-Addition−Electrocyclic Ring Closures Involving Acyclic α,β-Unsaturated Iminiums: A Formal [3 + 3] Cycloaddition Strategy to Unique Pyranyl Spirocycles-Reference-Cited by-同舟云学术

Sequential 1,2-Addition−Electrocyclic Ring Closures Involving Acyclic α,β-Unsaturated Iminiums: A Formal [3 + 3] Cycloaddition Strategy to Unique Pyranyl Spirocycles

Published:1999-01-08 Issue:3 Volume:64 Page:690-691
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Hsung Richard P.¹,Shen Hong C.¹,Douglas Christopher J.¹,Morgan Christopher D.¹,Degen Shane J.¹,Yao Letitia J.¹

Affiliation:

1. Department of Chemistry, The University of Minnesota, Minneapolis, Minnesota 55455

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo982165k

Reference13 articles.

1. UMN Undergraduate Research Participants, 1997−1998.

2. Recipient of 1998 Pharmacia-Upjohn Summer Fellowship.

3. Recipient of 1998 Pfizer Summer Fellowship.

4. Metal-Assisted Cycloaddition Reactions in Organotransition Metal Chemistry

5. The reactivity of 4-hydroxy-6-methyl-2-pyrone towards different types of ketones

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