Highly enantioselective aldol reactions catalyzed by a recyclable fluorous (S) pyrrolidine sulfonamide on water.Org Lett. 2008 Mar 20; 10(6):1211-4.OL
Abstract
Fluorous (S) pyrrolidine sulfonamide serves as an efficient promoter for highly enantioselective aldol reactions of ketones and aldehydes with aromatic aldehydes on water. A notable feature of the organocatalyst is that it can be recovered from the reaction mixtures by simple fluorous solid-phase extraction and subsequently reused (up to seven cycles) without a significant loss of catalytic activity and stereoselectivity.
Links
Pub Type(s)
Journal Article
Language
eng
PubMed ID
18271596
Citation
Zu, Liansuo, et al. "Highly Enantioselective Aldol Reactions Catalyzed By a Recyclable Fluorous (S) Pyrrolidine Sulfonamide On Water." Organic Letters, vol. 10, no. 6, 2008, pp. 1211-4.
Zu L, Xie H, Li H, et al. Highly enantioselective aldol reactions catalyzed by a recyclable fluorous (S) pyrrolidine sulfonamide on water. Org Lett. 2008;10(6):1211-4.
Zu, L., Xie, H., Li, H., Wang, J., & Wang, W. (2008). Highly enantioselective aldol reactions catalyzed by a recyclable fluorous (S) pyrrolidine sulfonamide on water. Organic Letters, 10(6), 1211-4. https://doi.org/10.1021/ol800074z
Zu L, et al. Highly Enantioselective Aldol Reactions Catalyzed By a Recyclable Fluorous (S) Pyrrolidine Sulfonamide On Water. Org Lett. 2008 Mar 20;10(6):1211-4. PubMed PMID: 18271596.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Highly enantioselective aldol reactions catalyzed by a recyclable fluorous (S) pyrrolidine sulfonamide on water.
AU - Zu,Liansuo,
AU - Xie,Hexin,
AU - Li,Hao,
AU - Wang,Jian,
AU - Wang,Wei,
Y1 - 2008/02/14/
PY - 2008/2/15/pubmed
PY - 2008/2/15/medline
PY - 2008/2/15/entrez
SP - 1211
EP - 4
JF - Organic letters
JO - Org Lett
VL - 10
IS - 6
N2 - Fluorous (S) pyrrolidine sulfonamide serves as an efficient promoter for highly enantioselective aldol reactions of ketones and aldehydes with aromatic aldehydes on water. A notable feature of the organocatalyst is that it can be recovered from the reaction mixtures by simple fluorous solid-phase extraction and subsequently reused (up to seven cycles) without a significant loss of catalytic activity and stereoselectivity.
SN - 1523-7060
UR - https://www.unboundmedicine.com/medline/citation/18271596/Highly_enantioselective_aldol_reactions_catalyzed_by_a_recyclable_fluorous__S__pyrrolidine_sulfonamide_on_water_
DB - PRIME
DP - Unbound Medicine
ER -