Synthesis of isoxazoles via electrophilic cyclization.Org Lett. 2005 Nov 10; 7(23):5203-5.OL
Abstract
[reaction: see text] A variety of 3,5-disubstituted 4-halo(seleno)isoxazoles are readily prepared in good to excellent yields under mild reaction conditions by the reaction of 2-alkyn-1-one O-methyl oximes with ICl, I2, Br2, or PhSeBr.
Pub Type(s)
Journal Article
Research Support, N.I.H., Extramural
Language
eng
PubMed ID
16268538
Citation
Waldo, Jesse P., and Richard C. Larock. "Synthesis of Isoxazoles Via Electrophilic Cyclization." Organic Letters, vol. 7, no. 23, 2005, pp. 5203-5.
Waldo JP, Larock RC. Synthesis of isoxazoles via electrophilic cyclization. Org Lett. 2005;7(23):5203-5.
Waldo, J. P., & Larock, R. C. (2005). Synthesis of isoxazoles via electrophilic cyclization. Organic Letters, 7(23), 5203-5.
Waldo JP, Larock RC. Synthesis of Isoxazoles Via Electrophilic Cyclization. Org Lett. 2005 Nov 10;7(23):5203-5. PubMed PMID: 16268538.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Synthesis of isoxazoles via electrophilic cyclization.
AU - Waldo,Jesse P,
AU - Larock,Richard C,
PY - 2005/11/5/pubmed
PY - 2006/8/10/medline
PY - 2005/11/5/entrez
SP - 5203
EP - 5
JF - Organic letters
JO - Org Lett
VL - 7
IS - 23
N2 - [reaction: see text] A variety of 3,5-disubstituted 4-halo(seleno)isoxazoles are readily prepared in good to excellent yields under mild reaction conditions by the reaction of 2-alkyn-1-one O-methyl oximes with ICl, I2, Br2, or PhSeBr.
SN - 1523-7060
UR - https://www.unboundmedicine.com/medline/citation/16268538/Synthesis_of_isoxazoles_via_electrophilic_cyclization_
DB - PRIME
DP - Unbound Medicine
ER -
