Anion-Controlled Stereoselective Synthesis of Cyclobutane Derivatives by Solid-State [2 + 2] Cycloaddition Reaction of the Salts of trans-3-(4-Pyridyl) Acrylic Acid-Reference-Cited by-同舟云学术

Anion-Controlled Stereoselective Synthesis of Cyclobutane Derivatives by Solid-State [2 + 2] Cycloaddition Reaction of the Salts of trans-3-(4-Pyridyl) Acrylic Acid

Published:2009-12-01 Issue:1 Volume:12 Page:128-131
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Kole Goutam Kumar¹,Tan Geok Kheng¹,Vittal Jagadese J.¹

Affiliation:

1. Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore 117543

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol9025233

Reference45 articles.

1. Some recent reviews:

2. Organic Synthesis in the Solid State via Hydrogen-Bond-Driven Self-Assembly

3. Stacking of double bonds for photochemical [2+2] cycloaddition reactions in the solid state

4. Crystal engineering principles applied to solution photochemistry: controlling the photodimerization of stilbazolium salts within γ-cyclodextrin and cucurbit[8]uril in water

5. Stereoselective Photodimerization of (E)-Stilbenes in Crystalline γ-Cyclodextrin Inclusion Complexes

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