Preparation of fully substituted anilines for the synthesis of functionalized indoles.Org Lett. 2008 Jan 03; 10(1):113-6.OL
Abstract
A wide range of highly functionalized indoles were prepared by the successive magnesiation of readily available o-alkynyl protected anilines using TMPMgCl.LiCl or LDA, followed by a KH-mediated cyclization reaction.
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
18069841
Citation
Stoll, Armin H., and Paul Knochel. "Preparation of Fully Substituted Anilines for the Synthesis of Functionalized Indoles." Organic Letters, vol. 10, no. 1, 2008, pp. 113-6.
Stoll AH, Knochel P. Preparation of fully substituted anilines for the synthesis of functionalized indoles. Org Lett. 2008;10(1):113-6.
Stoll, A. H., & Knochel, P. (2008). Preparation of fully substituted anilines for the synthesis of functionalized indoles. Organic Letters, 10(1), 113-6.
Stoll AH, Knochel P. Preparation of Fully Substituted Anilines for the Synthesis of Functionalized Indoles. Org Lett. 2008 Jan 3;10(1):113-6. PubMed PMID: 18069841.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Preparation of fully substituted anilines for the synthesis of functionalized indoles.
AU - Stoll,Armin H,
AU - Knochel,Paul,
Y1 - 2007/12/11/
PY - 2007/12/12/pubmed
PY - 2008/1/24/medline
PY - 2007/12/12/entrez
SP - 113
EP - 6
JF - Organic letters
JO - Org Lett
VL - 10
IS - 1
N2 - A wide range of highly functionalized indoles were prepared by the successive magnesiation of readily available o-alkynyl protected anilines using TMPMgCl.LiCl or LDA, followed by a KH-mediated cyclization reaction.
SN - 1523-7060
UR - https://www.unboundmedicine.com/medline/citation/18069841/Preparation_of_fully_substituted_anilines_for_the_synthesis_of_functionalized_indoles_
DB - PRIME
DP - Unbound Medicine
ER -
