Aluminum Chloride Catalyzed Stereoselective [3 + 2] Cycloaddition of Allylsilanes with Simple Conjugated Dienes-Reference-Cited by-同舟云学术

Aluminum Chloride Catalyzed Stereoselective [3 + 2] Cycloaddition of Allylsilanes with Simple Conjugated Dienes

Published:1997-11-01 Issue:24 Volume:16 Page:5158-5162
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Choi Geun Mook¹,Yeon Seoung Ho¹,Jin Jungil¹,Yoo Bok Ryul¹,Jung Il Nam¹

Affiliation:

1. Organometallic Chemistry Laboratory, Korea Institute of Science and Technology, P.O. Box 131 Cheongryang, Seoul 130-650, Korea, and Chemistry Department, Korea University, 1-Anam-dong, Seoul 136-701, Korea

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om970603s

Reference33 articles.

1. Cyclopentaannellation Reactions in Organic Synthesis

2. (b) Hudlicky, T.; Rulin, F.; Lovelace, T. C.; Reed J. W. InStudies in Natural Products Chemistry; Attauer-Raman, T., Ed.; Elsevier Science: Sussex, U.K, 1989; p 3.

3. Conjugate Addition of Allylsilanes with Subsequent Sila-Wagner-Meerwein Rearrangement: A Novel Methodology for Stereoselective Trimethylsilylcyclopentane Annulation

4. Transition Metal-Diene Complexes in Organic Synthesis; Part 6.1Stereoselective Synthesis of Iron-Complexed 4b,8a-Dihydrocarbazol-3-ones: A Novel Route to 4a,9a-Dihydro-9H-carbazoles and Highly Chemo-, Regio-, and Stereoselective Sakurai Reactions

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