Synthesis of novel β-aminocyclobutanecarboxylic acid derivatives by a solvent-free aza-Michael addition and subsequent ring closure
(2011) ORGANIC & BIOMOLECULAR CHEMISTRY. 9(20). p.7085-7091- abstract
- Novel beta-aminocyclobutanecarboxylic acid derivatives were prepared via a sequential solvent-free aza-Michael addition of benzophenone imine across 3-halopropylidenemalonates and base-induced ring closure. These highly substituted cyclobutanedicarboxylic acid derivatives were subjected to a reactivity study which demonstrated the tendency of these donor-acceptor substituted four-membered rings to be converted into their corresponding ring-opened products.
Please use this url to cite or link to this publication:
http://hdl.handle.net/1854/LU-1997584
- author
- Tamara Meiresonne UGent, Sven Mangelinckx UGent and Norbert De Kimpe UGent
- organization
- alternative title
- Synthesis of novel beta-aminocyclobutanecarboxylic acid derivatives by a solvent-free aza-Michael addition and subsequent ring closure
- year
- 2011
- type
- journalArticle (original)
- publication status
- published
- subject
- keyword
- 2-AMINOCYCLOBUTANECARBOXYLIC ACID, URACIL DERIVATIVES, AMINO-ACIDS, DIPEPTIDES, TRANSFORMATION, PHOTOCYCLOADDITION, CHEMISTRY, TETRAPEPTIDE, GAMMA-PEPTIDES, FOLDAMERS
- journal title
- ORGANIC & BIOMOLECULAR CHEMISTRY
- Org. Biomol. Chem.
- volume
- 9
- issue
- 20
- pages
- 7085 - 7091
- Web of Science type
- Article
- Web of Science id
- 000295889900034
- JCR category
- CHEMISTRY, ORGANIC
- JCR impact factor
- 3.696 (2011)
- JCR rank
- 11/56 (2011)
- JCR quartile
- 1 (2011)
- ISSN
- 1477-0520
- DOI
- 10.1039/c1ob05872j
- language
- English
- UGent publication?
- yes
- classification
- A1
- copyright statement
- I have transferred the copyright for this publication to the publisher
- id
- 1997584
- handle
- http://hdl.handle.net/1854/LU-1997584
- date created
- 2012-01-19 21:09:07
- date last changed
- 2012-07-14 00:30:43
@article{1997584,
abstract = {Novel beta-aminocyclobutanecarboxylic acid derivatives were prepared via a sequential solvent-free aza-Michael addition of benzophenone imine across 3-halopropylidenemalonates and base-induced ring closure. These highly substituted cyclobutanedicarboxylic acid derivatives were subjected to a reactivity study which demonstrated the tendency of these donor-acceptor substituted four-membered rings to be converted into their corresponding ring-opened products.},
author = {Meiresonne, Tamara and Mangelinckx, Sven and De Kimpe, Norbert},
issn = {1477-0520},
journal = {ORGANIC \& BIOMOLECULAR CHEMISTRY},
keyword = {2-AMINOCYCLOBUTANECARBOXYLIC ACID,URACIL DERIVATIVES,AMINO-ACIDS,DIPEPTIDES,TRANSFORMATION,PHOTOCYCLOADDITION,CHEMISTRY,TETRAPEPTIDE,GAMMA-PEPTIDES,FOLDAMERS},
language = {eng},
number = {20},
pages = {7085--7091},
title = {Synthesis of novel \ensuremath{\beta}-aminocyclobutanecarboxylic acid derivatives by a solvent-free aza-Michael addition and subsequent ring closure},
url = {http://dx.doi.org/10.1039/c1ob05872j},
volume = {9},
year = {2011},
}
- Chicago
- Meiresonne, Tamara, Sven Mangelinckx, and Norbert De Kimpe. 2011. “Synthesis of Novel Β-aminocyclobutanecarboxylic Acid Derivatives by a Solvent-free aza-Michael Addition and Subsequent Ring Closure.” Organic & Biomolecular Chemistry 9 (20): 7085–7091.
- APA
- Meiresonne, T., Mangelinckx, S., & De Kimpe, N. (2011). Synthesis of novel β-aminocyclobutanecarboxylic acid derivatives by a solvent-free aza-Michael addition and subsequent ring closure. ORGANIC & BIOMOLECULAR CHEMISTRY, 9(20), 7085–7091.
- Vancouver
- 1.Meiresonne T, Mangelinckx S, De Kimpe N. Synthesis of novel β-aminocyclobutanecarboxylic acid derivatives by a solvent-free aza-Michael addition and subsequent ring closure. ORGANIC & BIOMOLECULAR CHEMISTRY. 2011;9(20):7085–91.
- MLA
- Meiresonne, Tamara, Sven Mangelinckx, and Norbert De Kimpe. “Synthesis of Novel Β-aminocyclobutanecarboxylic Acid Derivatives by a Solvent-free aza-Michael Addition and Subsequent Ring Closure.” ORGANIC & BIOMOLECULAR CHEMISTRY 9.20 (2011): 7085–7091. Print.