One‐Pot Synthesis of Tetrahydro‐2‐Methylidenefurans
摘要:
Tetrahydro-2-methylidenefurans were prepared by the ring-opening/ recyclization reaction of 2-(disubstituted amino)-4,5-dihydro-3-furancarbonitriles with dichloroacetyl chloride in the presence of potassium carbonate.
One‐Pot Synthesis of Tetrahydro‐2‐Methylidenefurans
摘要:
Tetrahydro-2-methylidenefurans were prepared by the ring-opening/ recyclization reaction of 2-(disubstituted amino)-4,5-dihydro-3-furancarbonitriles with dichloroacetyl chloride in the presence of potassium carbonate.
One‐Pot Synthesis of Tetrahydro‐2‐Methylidenefurans
作者:Fumi Okabe、Yoshinobu Tagawa、Kenji Yamagata
DOI:10.1081/scc-200054188
日期:2005.4.1
Tetrahydro-2-methylidenefurans were prepared by the ring-opening/ recyclization reaction of 2-(disubstituted amino)-4,5-dihydro-3-furancarbonitriles with dichloroacetyl chloride in the presence of potassium carbonate.