4.4 Article

Heat Versus Basic Conditions: Intramolecular Dehydro-Diels-Alder Reaction of 1-Indolyl-1,6-heptadiynes for the Selective Synthesis of Substituted Carbazoles

期刊

SYNLETT
卷 28, 期 16, 页码 2189-2193

出版社

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0036-1588461

关键词

carbazoles; indoles; naphthalenes; dehydro-Diels-Alder reaction; intramolecular Diels-Alder reaction; chemoselectivity

资金

  1. JSPS KAKENHI [26410120]
  2. Grants-in-Aid for Scientific Research [26410120] Funding Source: KAKEN

向作者/读者索取更多资源

The intramolecular dehydro-Diels-Alder reaction of 1-indolyl-1,6-heptadiynes proceeds smoothly under rather mild heating conditions to give substituted carbazoles in moderate to good yields. The reaction of 7-aryl-1-indolyl-1,6-heptadiynes under heating gives the corresponding carbazoles chemoselectively in high yields, whereas the reaction under basic conditions gives naphthalenes as major products.

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