Gold(I)‐Catalyzed Reactions of 1‐(ortho‐Alkynylaryl)ureas: Highly Selective Heterocyclization and Synthesis of Mixed N, O‐Acetals. Issue 1 (8th January 2014)
- Record Type:
- Journal Article
- Title:
- Gold(I)‐Catalyzed Reactions of 1‐(ortho‐Alkynylaryl)ureas: Highly Selective Heterocyclization and Synthesis of Mixed N, O‐Acetals. Issue 1 (8th January 2014)
- Main Title:
- Gold(I)‐Catalyzed Reactions of 1‐(ortho‐Alkynylaryl)ureas: Highly Selective Heterocyclization and Synthesis of Mixed N, O‐Acetals
- Authors:
- Gimeno, Ana
Cuenca, Ana B.
Medio‐Simón, Mercedes
Asensio, Gregorio - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Readily available 1‐(<italic>ortho</italic>‐ethynylaryl)urea derivatives undergo a selective gold/silver {[AuCl(IPr)]/AgSbF<sub>6</sub>} catalyzed <italic>N</italic>‐6‐<italic>exo</italic>‐dig or <italic>N</italic>‐5‐<italic>endo</italic>‐dig heterocyclization process in dimethylformamide (DMF) at 60 °C. Benzoxazine derivatives, i.e., the products of <italic>O</italic>‐6‐<italic>exo</italic>‐dig ring closure through the urea oxygen, could be observed under catalytic conditions only when the <italic>N</italic>‐3 basicity was substantially diminished, but were readily isolable in stoichiometric processes carried out at low temperature. The open chain amino <italic>O</italic>, <italic>O</italic>‐acetals and a series of new cyclic mixed <italic>N</italic>, <italic>O</italic>‐acetals containing the trifluoroethyl group were synthesized when the reactions were performed in ethanol or trifluoroethanol, respectively, as solvent. The procedure allows for an easy access to this versatile class of key intermediates in organic synthesis from simple starting materials. The effect of using either DMF or protic solvents on the course of the reactions is reported.</p> <p> <boxed-text content-type="graphic" position="anchor" orientation="portrait"> <graphic position="anchor" mimetype="image" xlink:href="ark:/27927/pgg4sm49640" orientation="portrait" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" /><abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Readily available 1‐(<italic>ortho</italic>‐ethynylaryl)urea derivatives undergo a selective gold/silver {[AuCl(IPr)]/AgSbF<sub>6</sub>} catalyzed <italic>N</italic>‐6‐<italic>exo</italic>‐dig or <italic>N</italic>‐5‐<italic>endo</italic>‐dig heterocyclization process in dimethylformamide (DMF) at 60 °C. Benzoxazine derivatives, i.e., the products of <italic>O</italic>‐6‐<italic>exo</italic>‐dig ring closure through the urea oxygen, could be observed under catalytic conditions only when the <italic>N</italic>‐3 basicity was substantially diminished, but were readily isolable in stoichiometric processes carried out at low temperature. The open chain amino <italic>O</italic>, <italic>O</italic>‐acetals and a series of new cyclic mixed <italic>N</italic>, <italic>O</italic>‐acetals containing the trifluoroethyl group were synthesized when the reactions were performed in ethanol or trifluoroethanol, respectively, as solvent. The procedure allows for an easy access to this versatile class of key intermediates in organic synthesis from simple starting materials. The effect of using either DMF or protic solvents on the course of the reactions is reported.</p> <p> <boxed-text content-type="graphic" position="anchor" orientation="portrait"> <graphic position="anchor" mimetype="image" xlink:href="ark:/27927/pgg4sm49640" orientation="portrait" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" /> </boxed-text> </p> </abstract> … (more)
- Is Part Of:
- Advanced synthesis & catalysis. Volume 356:Issue 1(2014)
- Journal:
- Advanced synthesis & catalysis
- Issue:
- Volume 356:Issue 1(2014)
- Issue Display:
- Volume 356, Issue 1 (2014)
- Year:
- 2014
- Volume:
- 356
- Issue:
- 1
- Issue Sort Value:
- 2014-0356-0001-0000
- Page Start:
- 229
- Page End:
- 236
- Publication Date:
- 2014-01-08
- Subjects:
- Catalysis -- Periodicals
Organic compounds -- Synthesis -- Periodicals
Chemistry -- Periodicals
Chemistry, Technical -- Periodicals
Chemistry -- Periodicals
Catalysis -- Periodicals
Technology, Pharmaceutical -- Periodicals
547.2 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1615-4169 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/adsc.201300730 ↗
- Languages:
- English
- ISSNs:
- 1615-4150
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0696.931980
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3052.xml