Enantioselective phenylacetylene addition to aldehydes and ketones catalyzed by recyclable polymeric Zn(salen) complex.Chirality. 2007 Jan; 19(1):82-8.C
Abstract
New polymeric Zn(salen) complex was employed in the enantioselective phenylacetylene addition to aldehydes and ketones to produce corresponding chiral secondary propargylic alcohols with yields (up to 96%) and enantioselectivity (up to 72%) and tertiary propargylic alcohols with yields (up to 79%) and enantioselectivity (up to 68%) at room temperature, with added advantage of four times reuse with retention of enantioselectivity.
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
17094071
Citation
Pathak, Kavita, et al. "Enantioselective Phenylacetylene Addition to Aldehydes and Ketones Catalyzed By Recyclable Polymeric Zn(salen) Complex." Chirality, vol. 19, no. 1, 2007, pp. 82-8.
Pathak K, Bhatt AP, Abdi SH, et al. Enantioselective phenylacetylene addition to aldehydes and ketones catalyzed by recyclable polymeric Zn(salen) complex. Chirality. 2007;19(1):82-8.
Pathak, K., Bhatt, A. P., Abdi, S. H., Kureshy, R. I., Khan, N. U., Ahmad, I., & Jasra, R. V. (2007). Enantioselective phenylacetylene addition to aldehydes and ketones catalyzed by recyclable polymeric Zn(salen) complex. Chirality, 19(1), 82-8.
Pathak K, et al. Enantioselective Phenylacetylene Addition to Aldehydes and Ketones Catalyzed By Recyclable Polymeric Zn(salen) Complex. Chirality. 2007;19(1):82-8. PubMed PMID: 17094071.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Enantioselective phenylacetylene addition to aldehydes and ketones catalyzed by recyclable polymeric Zn(salen) complex.
AU - Pathak,Kavita,
AU - Bhatt,Achyut P,
AU - Abdi,Sayed H R,
AU - Kureshy,Rukhsana I,
AU - Khan,Noor-Ul H,
AU - Ahmad,Irshad,
AU - Jasra,Raksh V,
PY - 2006/11/10/pubmed
PY - 2007/1/16/medline
PY - 2006/11/10/entrez
SP - 82
EP - 8
JF - Chirality
JO - Chirality
VL - 19
IS - 1
N2 - New polymeric Zn(salen) complex was employed in the enantioselective phenylacetylene addition to aldehydes and ketones to produce corresponding chiral secondary propargylic alcohols with yields (up to 96%) and enantioselectivity (up to 72%) and tertiary propargylic alcohols with yields (up to 79%) and enantioselectivity (up to 68%) at room temperature, with added advantage of four times reuse with retention of enantioselectivity.
SN - 0899-0042
UR - https://www.unboundmedicine.com/medline/citation/17094071/Enantioselective_phenylacetylene_addition_to_aldehydes_and_ketones_catalyzed_by_recyclable_polymeric_Zn_salen__complex_
L2 - https://doi.org/10.1002/chir.20337
DB - PRIME
DP - Unbound Medicine
ER -