Synthesis of 2,3-disubstituted indoles by a rhodium-catalyzed aromatic amino-Claisen rearrangement of N-propargyl anilines.Angew Chem Int Ed Engl. 2007; 46(21):3931-3.AC
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
17427902
Citation
Saito, Akio, et al. "Synthesis of 2,3-disubstituted Indoles By a Rhodium-catalyzed Aromatic amino-Claisen Rearrangement of N-propargyl Anilines." Angewandte Chemie (International Ed. in English), vol. 46, no. 21, 2007, pp. 3931-3.
Saito A, Kanno A, Hanzawa Y. Synthesis of 2,3-disubstituted indoles by a rhodium-catalyzed aromatic amino-Claisen rearrangement of N-propargyl anilines. Angew Chem Int Ed Engl. 2007;46(21):3931-3.
Saito, A., Kanno, A., & Hanzawa, Y. (2007). Synthesis of 2,3-disubstituted indoles by a rhodium-catalyzed aromatic amino-Claisen rearrangement of N-propargyl anilines. Angewandte Chemie (International Ed. in English), 46(21), 3931-3.
Saito A, Kanno A, Hanzawa Y. Synthesis of 2,3-disubstituted Indoles By a Rhodium-catalyzed Aromatic amino-Claisen Rearrangement of N-propargyl Anilines. Angew Chem Int Ed Engl. 2007;46(21):3931-3. PubMed PMID: 17427902.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Synthesis of 2,3-disubstituted indoles by a rhodium-catalyzed aromatic amino-Claisen rearrangement of N-propargyl anilines.
AU - Saito,Akio,
AU - Kanno,Ayumi,
AU - Hanzawa,Yuji,
PY - 2007/4/13/pubmed
PY - 2007/8/19/medline
PY - 2007/4/13/entrez
SP - 3931
EP - 3
JF - Angewandte Chemie (International ed. in English)
JO - Angew Chem Int Ed Engl
VL - 46
IS - 21
SN - 1433-7851
UR - https://www.unboundmedicine.com/medline/citation/17427902/Synthesis_of_23_disubstituted_indoles_by_a_rhodium_catalyzed_aromatic_amino_Claisen_rearrangement_of_N_propargyl_anilines_
L2 - https://doi.org/10.1002/anie.200605162
DB - PRIME
DP - Unbound Medicine
ER -