Synthesis of polycyclic aromatics and heteroaromatics via electrophilic cyclization.J Org Chem. 2005 Apr 29; 70(9):3511-7.JO
Abstract
[reaction: see text] A variety of substituted polycyclic aromatics are readily prepared in good to excellent yields under very mild reaction conditions by the reaction of 2-(1-alkynyl)biphenyls with ICl, I(2), NBS, and p-O(2)NC(6)H(4)SCl. This methodology readily accommodates various functional groups and has been successfully extended to systems containing a variety of polycyclic and heterocyclic rings.
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Research Support, U.S. Gov't, P.H.S.
Language
eng
PubMed ID
15844984
Citation
Yao, Tuanli, et al. "Synthesis of Polycyclic Aromatics and Heteroaromatics Via Electrophilic Cyclization." The Journal of Organic Chemistry, vol. 70, no. 9, 2005, pp. 3511-7.
Yao T, Campo MA, Larock RC. Synthesis of polycyclic aromatics and heteroaromatics via electrophilic cyclization. J Org Chem. 2005;70(9):3511-7.
Yao, T., Campo, M. A., & Larock, R. C. (2005). Synthesis of polycyclic aromatics and heteroaromatics via electrophilic cyclization. The Journal of Organic Chemistry, 70(9), 3511-7.
Yao T, Campo MA, Larock RC. Synthesis of Polycyclic Aromatics and Heteroaromatics Via Electrophilic Cyclization. J Org Chem. 2005 Apr 29;70(9):3511-7. PubMed PMID: 15844984.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Synthesis of polycyclic aromatics and heteroaromatics via electrophilic cyclization.
AU - Yao,Tuanli,
AU - Campo,Marino A,
AU - Larock,Richard C,
PY - 2005/4/23/pubmed
PY - 2005/5/25/medline
PY - 2005/4/23/entrez
SP - 3511
EP - 7
JF - The Journal of organic chemistry
JO - J Org Chem
VL - 70
IS - 9
N2 - [reaction: see text] A variety of substituted polycyclic aromatics are readily prepared in good to excellent yields under very mild reaction conditions by the reaction of 2-(1-alkynyl)biphenyls with ICl, I(2), NBS, and p-O(2)NC(6)H(4)SCl. This methodology readily accommodates various functional groups and has been successfully extended to systems containing a variety of polycyclic and heterocyclic rings.
SN - 0022-3263
UR - https://www.unboundmedicine.com/medline/citation/15844984/Synthesis_of_polycyclic_aromatics_and_heteroaromatics_via_electrophilic_cyclization_
DB - PRIME
DP - Unbound Medicine
ER -