Palladium asymmetric allylic alkylation of prochiral nucleophiles: horsfiline.Org Lett. 2006 May 11; 8(10):2027-30.OL
Abstract
[reaction; see text] The asymmetric synthesis of the oxindole alkaloid horsfiline is described. A palladium-catalyzed asymmetric allylic alkylation (AAA) is used to set the spiro(pyrrolidine-oxindole) stereogenic center.
Links
Pub Type(s)
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S.
Language
eng
PubMed ID
16671773
Citation
Trost, Barry M., and Megan K. Brennan. "Palladium Asymmetric Allylic Alkylation of Prochiral Nucleophiles: Horsfiline." Organic Letters, vol. 8, no. 10, 2006, pp. 2027-30.
Trost BM, Brennan MK. Palladium asymmetric allylic alkylation of prochiral nucleophiles: horsfiline. Org Lett. 2006;8(10):2027-30.
Trost, B. M., & Brennan, M. K. (2006). Palladium asymmetric allylic alkylation of prochiral nucleophiles: horsfiline. Organic Letters, 8(10), 2027-30.
Trost BM, Brennan MK. Palladium Asymmetric Allylic Alkylation of Prochiral Nucleophiles: Horsfiline. Org Lett. 2006 May 11;8(10):2027-30. PubMed PMID: 16671773.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Palladium asymmetric allylic alkylation of prochiral nucleophiles: horsfiline.
AU - Trost,Barry M,
AU - Brennan,Megan K,
PY - 2006/5/5/pubmed
PY - 2007/2/16/medline
PY - 2006/5/5/entrez
SP - 2027
EP - 30
JF - Organic letters
JO - Org Lett
VL - 8
IS - 10
N2 - [reaction; see text] The asymmetric synthesis of the oxindole alkaloid horsfiline is described. A palladium-catalyzed asymmetric allylic alkylation (AAA) is used to set the spiro(pyrrolidine-oxindole) stereogenic center.
SN - 1523-7060
UR - https://www.unboundmedicine.com/medline/citation/16671773/Palladium_asymmetric_allylic_alkylation_of_prochiral_nucleophiles:_horsfiline_
DB - PRIME
DP - Unbound Medicine
ER -