Facile synthesis of diiodinated dihydronaphthalenes and naphthalenes via iodine mediated electrophilic cyclization.Chem Commun (Camb). 2011 Apr 07; 47(13):4013-5.CC
Abstract
A facile, efficient, and general synthetic method for a wide range of 2,3-diiodinated 1,4-dihydrothiophenes and naphthalenes has been developed via the electrophilic iodocyclization of various aryl propargyl alcohols. The resulting product 2p can be used for the synthesis of a rubrene intermediate.
Links
Pub Type(s)
Journal Article
Language
eng
PubMed ID
21336384
Citation
Yang, Fan, et al. "Facile Synthesis of Diiodinated Dihydronaphthalenes and Naphthalenes Via Iodine Mediated Electrophilic Cyclization." Chemical Communications (Cambridge, England), vol. 47, no. 13, 2011, pp. 4013-5.
Yang F, Jin T, Bao M, et al. Facile synthesis of diiodinated dihydronaphthalenes and naphthalenes via iodine mediated electrophilic cyclization. Chem Commun (Camb). 2011;47(13):4013-5.
Yang, F., Jin, T., Bao, M., & Yamamoto, Y. (2011). Facile synthesis of diiodinated dihydronaphthalenes and naphthalenes via iodine mediated electrophilic cyclization. Chemical Communications (Cambridge, England), 47(13), 4013-5. https://doi.org/10.1039/c0cc05442a
Yang F, et al. Facile Synthesis of Diiodinated Dihydronaphthalenes and Naphthalenes Via Iodine Mediated Electrophilic Cyclization. Chem Commun (Camb). 2011 Apr 7;47(13):4013-5. PubMed PMID: 21336384.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Facile synthesis of diiodinated dihydronaphthalenes and naphthalenes via iodine mediated electrophilic cyclization.
AU - Yang,Fan,
AU - Jin,Tienan,
AU - Bao,Ming,
AU - Yamamoto,Yoshinori,
Y1 - 2011/02/21/
PY - 2011/2/22/entrez
PY - 2011/2/22/pubmed
PY - 2011/2/22/medline
SP - 4013
EP - 5
JF - Chemical communications (Cambridge, England)
JO - Chem Commun (Camb)
VL - 47
IS - 13
N2 - A facile, efficient, and general synthetic method for a wide range of 2,3-diiodinated 1,4-dihydrothiophenes and naphthalenes has been developed via the electrophilic iodocyclization of various aryl propargyl alcohols. The resulting product 2p can be used for the synthesis of a rubrene intermediate.
SN - 1364-548X
UR - https://www.unboundmedicine.com/medline/citation/21336384/Facile_synthesis_of_diiodinated_dihydronaphthalenes_and_naphthalenes_via_iodine_mediated_electrophilic_cyclization_
DB - PRIME
DP - Unbound Medicine
ER -
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