Facile formation of cyclic aminals through a Brønsted acid-promoted redox process.J Org Chem. 2009 Jan 02; 74(1):419-22.JO
Abstract
Cyclic aminals were prepared through a Brønsted acid-promoted reaction. This redox neutral process involves iminium ion formation, 1,5 H-transfer, followed by ring closure.
Links
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
19053590
Citation
Zhang, Chen, et al. "Facile Formation of Cyclic Aminals Through a Brønsted Acid-promoted Redox Process." The Journal of Organic Chemistry, vol. 74, no. 1, 2009, pp. 419-22.
Zhang C, Murarka S, Seidel D. Facile formation of cyclic aminals through a Brønsted acid-promoted redox process. J Org Chem. 2009;74(1):419-22.
Zhang, C., Murarka, S., & Seidel, D. (2009). Facile formation of cyclic aminals through a Brønsted acid-promoted redox process. The Journal of Organic Chemistry, 74(1), 419-22. https://doi.org/10.1021/jo802325x
Zhang C, Murarka S, Seidel D. Facile Formation of Cyclic Aminals Through a Brønsted Acid-promoted Redox Process. J Org Chem. 2009 Jan 2;74(1):419-22. PubMed PMID: 19053590.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Facile formation of cyclic aminals through a Brønsted acid-promoted redox process.
AU - Zhang,Chen,
AU - Murarka,Sandip,
AU - Seidel,Daniel,
PY - 2008/12/5/pubmed
PY - 2009/2/13/medline
PY - 2008/12/5/entrez
SP - 419
EP - 22
JF - The Journal of organic chemistry
JO - J Org Chem
VL - 74
IS - 1
N2 - Cyclic aminals were prepared through a Brønsted acid-promoted reaction. This redox neutral process involves iminium ion formation, 1,5 H-transfer, followed by ring closure.
SN - 1520-6904
UR - https://www.unboundmedicine.com/medline/citation/19053590/Facile_formation_of_cyclic_aminals_through_a_Brønsted_acid_promoted_redox_process_
L2 - https://doi.org/10.1021/jo802325x
DB - PRIME
DP - Unbound Medicine
ER -