Copper(I)-secondary diamine complex-catalyzed enantioselective conjugate boration of linear β,β-disubstituted enones.Org Lett. 2010 Sep 17; 12(18):4098-101.OL
Abstract
A copper(I)-chiral secondary diamine (L-e) complex catalyzes an enantioselective conjugate boration of β,β-disubstituted enones in high yields and up to 99% ee. Product chiral tertiary organoboronates can be converted to enantiomerically enriched cross-aldol products between ketones without any racemization.
Links
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
20722382
Citation
Chen, I-Hon, et al. "Copper(I)-secondary Diamine Complex-catalyzed Enantioselective Conjugate Boration of Linear Β,β-disubstituted Enones." Organic Letters, vol. 12, no. 18, 2010, pp. 4098-101.
Chen IH, Kanai M, Shibasaki M. Copper(I)-secondary diamine complex-catalyzed enantioselective conjugate boration of linear β,β-disubstituted enones. Org Lett. 2010;12(18):4098-101.
Chen, I. H., Kanai, M., & Shibasaki, M. (2010). Copper(I)-secondary diamine complex-catalyzed enantioselective conjugate boration of linear β,β-disubstituted enones. Organic Letters, 12(18), 4098-101. https://doi.org/10.1021/ol101691p
Chen IH, Kanai M, Shibasaki M. Copper(I)-secondary Diamine Complex-catalyzed Enantioselective Conjugate Boration of Linear Β,β-disubstituted Enones. Org Lett. 2010 Sep 17;12(18):4098-101. PubMed PMID: 20722382.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Copper(I)-secondary diamine complex-catalyzed enantioselective conjugate boration of linear β,β-disubstituted enones.
AU - Chen,I-Hon,
AU - Kanai,Motomu,
AU - Shibasaki,Masakatsu,
PY - 2010/8/21/entrez
PY - 2010/8/21/pubmed
PY - 2010/12/22/medline
SP - 4098
EP - 101
JF - Organic letters
JO - Org Lett
VL - 12
IS - 18
N2 - A copper(I)-chiral secondary diamine (L-e) complex catalyzes an enantioselective conjugate boration of β,β-disubstituted enones in high yields and up to 99% ee. Product chiral tertiary organoboronates can be converted to enantiomerically enriched cross-aldol products between ketones without any racemization.
SN - 1523-7052
UR - https://www.unboundmedicine.com/medline/citation/20722382/Copper_I__secondary_diamine_complex_catalyzed_enantioselective_conjugate_boration_of_linear_����_disubstituted_enones_
L2 - https://doi.org/10.1021/ol101691p
DB - PRIME
DP - Unbound Medicine
ER -