Lewis Acid-Catalyzed Intramolecular [2 + 2] Cycloaddition of α-Ester-Substituted Conjugated Dienyl- and Trienylphosphonates. New Synthesis of Functionalized Cyclic Terpenoids-Reference-Cited by-同舟云学术

Lewis Acid-Catalyzed Intramolecular [2 + 2] Cycloaddition of α-Ester-Substituted Conjugated Dienyl- and Trienylphosphonates. New Synthesis of Functionalized Cyclic Terpenoids

Published:1997-11-01 Issue:24 Volume:62 Page:8419-8424
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Okauchi Tatsuo¹,Kakiuchi Toshihito¹,Kitamura Naotaka¹,Utsunomiya Tomohisa¹,Ichikawa Junji¹,Minami Toru¹

Affiliation:

1. Department of Applied Chemistry, Kyushu Institute of Technology, Sensuicho, Tobata, Kitakyushu 804, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo971153g

Reference19 articles.

1. Vinylphosphonates in Organic Synthesis

2. Conjugate Addition of Organocuprates to Diethyl Vinylphosphonate

3. Phosphonates as analogues of natural phosphates

4. Novel acyclonucleotides: synthesis and antiviral activity of alkenylphosphonic acid derivatives of purines and a pyrimidine

5. Synthesis and properties of adenosine oligonucleotide analogs containing methylene groups in place of phosphodiester 5'-oxygens

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