Asymmetric addition of phenylacetylene to aromatic ketones catalyzed by zinc or titanium complexes with chiral hydroxysulfonamide.Chirality. 2009 Apr; 21(4):473-9.C
Abstract
Various new chiral hydroxysulfonamide ligands (3a-3n, 4a-4d) were prepared. Compounds 3a, 3g, 3i, 3k-3n, 4a-4d could accelerate the reaction and reduce reaction time, and 3a, 3g, 3i, 3k-3n catalyzed the reaction without titanium. The results obtained were promising in terms of yields and enantiomeric excesses (3k up to 85% ee, 4a up to 83% ee).
Links
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
18655167
Citation
Zhou, Yi-Feng, et al. "Asymmetric Addition of Phenylacetylene to Aromatic Ketones Catalyzed By Zinc or Titanium Complexes With Chiral Hydroxysulfonamide." Chirality, vol. 21, no. 4, 2009, pp. 473-9.
Zhou YF, Han ZJ, Qiu L, et al. Asymmetric addition of phenylacetylene to aromatic ketones catalyzed by zinc or titanium complexes with chiral hydroxysulfonamide. Chirality. 2009;21(4):473-9.
Zhou, Y. F., Han, Z. J., Qiu, L., Liang, J. Y., Ren, F. B., & Wang, R. (2009). Asymmetric addition of phenylacetylene to aromatic ketones catalyzed by zinc or titanium complexes with chiral hydroxysulfonamide. Chirality, 21(4), 473-9. https://doi.org/10.1002/chir.20622
Zhou YF, et al. Asymmetric Addition of Phenylacetylene to Aromatic Ketones Catalyzed By Zinc or Titanium Complexes With Chiral Hydroxysulfonamide. Chirality. 2009;21(4):473-9. PubMed PMID: 18655167.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Asymmetric addition of phenylacetylene to aromatic ketones catalyzed by zinc or titanium complexes with chiral hydroxysulfonamide.
AU - Zhou,Yi-Feng,
AU - Han,Zhi-Jian,
AU - Qiu,Li,
AU - Liang,Jin-Yan,
AU - Ren,Feng-Bo,
AU - Wang,Rui,
PY - 2008/7/26/pubmed
PY - 2009/8/25/medline
PY - 2008/7/26/entrez
SP - 473
EP - 9
JF - Chirality
JO - Chirality
VL - 21
IS - 4
N2 - Various new chiral hydroxysulfonamide ligands (3a-3n, 4a-4d) were prepared. Compounds 3a, 3g, 3i, 3k-3n, 4a-4d could accelerate the reaction and reduce reaction time, and 3a, 3g, 3i, 3k-3n catalyzed the reaction without titanium. The results obtained were promising in terms of yields and enantiomeric excesses (3k up to 85% ee, 4a up to 83% ee).
SN - 1520-636X
UR - https://www.unboundmedicine.com/medline/citation/18655167/Asymmetric_addition_of_phenylacetylene_to_aromatic_ketones_catalyzed_by_zinc_or_titanium_complexes_with_chiral_hydroxysulfonamide_
L2 - https://doi.org/10.1002/chir.20622
DB - PRIME
DP - Unbound Medicine
ER -