Selectivity in Garratt–Braverman Cyclization of Aryl-/Heteroaryl-Substituted Unsymmetrical Bis-Propargyl Systems: Formal Synthesis of 7′-Desmethylkealiiquinone-Reference-Cited by-同舟云学术

Selectivity in Garratt–Braverman Cyclization of Aryl-/Heteroaryl-Substituted Unsymmetrical Bis-Propargyl Systems: Formal Synthesis of 7′-Desmethylkealiiquinone

Published:2014-04-14 Issue:9 Volume:79 Page:3789-3798
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Das Joyee¹,Mukherjee Raja¹,Basak Amit¹

Affiliation:

1. Department of Chemistry, Indian Institute of Technology, Kharagpur 721 302, India

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo402749d

Reference36 articles.

1. Strained heterocycles. Properties of five-membered heterocycles fused to four-, six-, and eight-membered rings prepared by base-catalyzed rearrangement of 4-heterohepta-1,6-diynes

2. Synthesis and Thermal Rearrangement of 4-Heterohepta-1,2,5,6-tetraenes

3. Cycloaromatization and cyclodimerization of bridged diallenes

4. Sequential Intermediates in the Base-Catalyzed Conversion of Bis(π-conjugated propargyl) Sulfones to 1,3-Dihydrobenzo- and Naphtho[c]thiophene-2,2-dioxides

5. A one-pot Garratt–Braverman cyclization and Scholl oxidation route to acene–helicene hybrids

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