New MCR-Heck-isomerization cascade toward indoles.Org Lett. 2008 Aug 21; 10(16):3417-9.OL
Abstract
The use of ortho-iodonitrophenol in Ugi-Smiles reaction coupled with Heck cyclization gives new access to indole scaffolds. The sequence can be performed in a one-pot reaction if the residual isocyanide is neutralized prior to the addition of the palladium catalyst.
Links
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
18616343
Citation
El Kaim, Laurent, et al. "New MCR-Heck-isomerization Cascade Toward Indoles." Organic Letters, vol. 10, no. 16, 2008, pp. 3417-9.
El Kaim L, Gizzi M, Grimaud L. New MCR-Heck-isomerization cascade toward indoles. Org Lett. 2008;10(16):3417-9.
El Kaim, L., Gizzi, M., & Grimaud, L. (2008). New MCR-Heck-isomerization cascade toward indoles. Organic Letters, 10(16), 3417-9. https://doi.org/10.1021/ol801217a
El Kaim L, Gizzi M, Grimaud L. New MCR-Heck-isomerization Cascade Toward Indoles. Org Lett. 2008 Aug 21;10(16):3417-9. PubMed PMID: 18616343.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - New MCR-Heck-isomerization cascade toward indoles.
AU - El Kaim,Laurent,
AU - Gizzi,Marion,
AU - Grimaud,Laurence,
Y1 - 2008/07/11/
PY - 2008/7/12/pubmed
PY - 2008/10/22/medline
PY - 2008/7/12/entrez
SP - 3417
EP - 9
JF - Organic letters
JO - Org Lett
VL - 10
IS - 16
N2 - The use of ortho-iodonitrophenol in Ugi-Smiles reaction coupled with Heck cyclization gives new access to indole scaffolds. The sequence can be performed in a one-pot reaction if the residual isocyanide is neutralized prior to the addition of the palladium catalyst.
SN - 1523-7052
UR - https://www.unboundmedicine.com/medline/citation/18616343/New_MCR_Heck_isomerization_cascade_toward_indoles_
L2 - https://doi.org/10.1021/ol801217a
DB - PRIME
DP - Unbound Medicine
ER -
