A recyclable fluorous organocatalyst for Diels-Alder reactions.Tetrahedron Lett. 2006 Dec 25; 47(52):9287-9290.TL
Abstract
Chiral fluorous imidazolidinone catalyst 2 provides consistently high enantioselectivities in Diels-Alder reactions of dienes and alpha, beta-unsaturated aldehydes. The catalyst can be readily separated from the reaction products by fluorous solid-phase extraction, and recovered in excellent purity for direct reuse.
Links
Pub Type(s)
Journal Article
Language
eng
PubMed ID
17710220
Citation
Chu, Qianli, et al. "A Recyclable Fluorous Organocatalyst for Diels-Alder Reactions." Tetrahedron Letters, vol. 47, no. 52, 2006, pp. 9287-9290.
Chu Q, Zhang W, Curran DP. A recyclable fluorous organocatalyst for Diels-Alder reactions. Tetrahedron Lett. 2006;47(52):9287-9290.
Chu, Q., Zhang, W., & Curran, D. P. (2006). A recyclable fluorous organocatalyst for Diels-Alder reactions. Tetrahedron Letters, 47(52), 9287-9290.
Chu Q, Zhang W, Curran DP. A Recyclable Fluorous Organocatalyst for Diels-Alder Reactions. Tetrahedron Lett. 2006 Dec 25;47(52):9287-9290. PubMed PMID: 17710220.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - A recyclable fluorous organocatalyst for Diels-Alder reactions.
AU - Chu,Qianli,
AU - Zhang,Wei,
AU - Curran,Dennis P,
PY - 2007/8/22/pubmed
PY - 2007/8/22/medline
PY - 2007/8/22/entrez
SP - 9287
EP - 9290
JF - Tetrahedron letters
JO - Tetrahedron Lett
VL - 47
IS - 52
N2 - Chiral fluorous imidazolidinone catalyst 2 provides consistently high enantioselectivities in Diels-Alder reactions of dienes and alpha, beta-unsaturated aldehydes. The catalyst can be readily separated from the reaction products by fluorous solid-phase extraction, and recovered in excellent purity for direct reuse.
SN - 0040-4039
UR - https://www.unboundmedicine.com/medline/citation/17710220/A_recyclable_fluorous_organocatalyst_for_Diels_Alder_reactions_
L2 - https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/17710220/
DB - PRIME
DP - Unbound Medicine
ER -