De Novo and Divergent Synthesis of Highly Functionalized Furans by Cascade Reactions of 2‐Hydroxy‐1, 4‐diones with Nucleophiles. Issue 16 (22nd February 2021)
- Record Type:
- Journal Article
- Title:
- De Novo and Divergent Synthesis of Highly Functionalized Furans by Cascade Reactions of 2‐Hydroxy‐1, 4‐diones with Nucleophiles. Issue 16 (22nd February 2021)
- Main Title:
- De Novo and Divergent Synthesis of Highly Functionalized Furans by Cascade Reactions of 2‐Hydroxy‐1, 4‐diones with Nucleophiles
- Authors:
- Liu, Hai‐xuan
Ji, Fei
Chen, Yu
Gao, Ya
Wang, Jun‐ke
Zhang, Ming‐zhi
Liu, Fang
Sha, Qiang - Abstract:
- Abstract: Herein, a divergent synthesis of a variety of 2α‐ and 5α‐substituted furan derivatives from 2‐hydroxy‐1, 4‐diones is reported. By using appropriate substrates and an acid catalyst, the reactions occurred selectively through cyclization/1, 6‐conjugate addition or cyclization/Friedel–Crafts‐type cascade reactions. A broad range of nucleophilic reagents (>10 types for the 1, 6‐conjugate addition for 5α substitution and >20 types for the Friedel–Crafts‐type cascade reaction for 2α substitution), including alcohols, amides, furan, thiophene, pyrrole, indole, phenols, and many others, can successfully participate in the reactions, providing a universal strategy for a diversity‐oriented synthesis of α‐substituted furan derivatives. Deuteriation experiments and DFT calculations were carried out to support the proposed reaction mechanisms. Antifungal activity experiments revealed that products with an indole or 4‐hydroxycoumarin core substituted at the 2α position showed moderate activities against Rhizoctorzia solani and Botrytis cinerea, respectively. Abstract : Great selection ! We present herein a de novo and divergent synthesis of 2α‐ and 5α‐substituted furans from 2‐hydroxy‐1, 4‐diones and a variety of nucleophiles with good regio‐ and chemoselectivity, as well as a very broad substrate scope (>10 types of nucleophiles for the 5α functionalization and >20 types of nucleophiles for the 2α functionalization; see scheme). The products show good potential as antifungalAbstract: Herein, a divergent synthesis of a variety of 2α‐ and 5α‐substituted furan derivatives from 2‐hydroxy‐1, 4‐diones is reported. By using appropriate substrates and an acid catalyst, the reactions occurred selectively through cyclization/1, 6‐conjugate addition or cyclization/Friedel–Crafts‐type cascade reactions. A broad range of nucleophilic reagents (>10 types for the 1, 6‐conjugate addition for 5α substitution and >20 types for the Friedel–Crafts‐type cascade reaction for 2α substitution), including alcohols, amides, furan, thiophene, pyrrole, indole, phenols, and many others, can successfully participate in the reactions, providing a universal strategy for a diversity‐oriented synthesis of α‐substituted furan derivatives. Deuteriation experiments and DFT calculations were carried out to support the proposed reaction mechanisms. Antifungal activity experiments revealed that products with an indole or 4‐hydroxycoumarin core substituted at the 2α position showed moderate activities against Rhizoctorzia solani and Botrytis cinerea, respectively. Abstract : Great selection ! We present herein a de novo and divergent synthesis of 2α‐ and 5α‐substituted furans from 2‐hydroxy‐1, 4‐diones and a variety of nucleophiles with good regio‐ and chemoselectivity, as well as a very broad substrate scope (>10 types of nucleophiles for the 5α functionalization and >20 types of nucleophiles for the 2α functionalization; see scheme). The products show good potential as antifungal agents. … (more)
- Is Part Of:
- Chemistry. Volume 27:Issue 16(2021)
- Journal:
- Chemistry
- Issue:
- Volume 27:Issue 16(2021)
- Issue Display:
- Volume 27, Issue 16 (2021)
- Year:
- 2021
- Volume:
- 27
- Issue:
- 16
- Issue Sort Value:
- 2021-0027-0016-0000
- Page Start:
- 5225
- Page End:
- 5229
- Publication Date:
- 2021-02-22
- Subjects:
- carbocations -- cyclization reactions -- nucleophilic addition -- oxygen heterocycles -- reaction mechanisms -- regioselectivity
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.202005098 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 22427.xml