1b-D, 1,8-Deutero-octa-1,7-diyne
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NMR data
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创建时间：
2023-03-01
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3,3,6,6-Tetramethyl-octa-1,7-diyne
This page, "3,3,6,6-Tetramethyl-octa-1,7-diyne", is part of the NIST Chemistry WebBook. This site and its contents are part of the NIST Standard Reference Data Program.
webbook.nist.gov40
Gold-Catalyzed Cycloisomerization of 1,7-Diyne Benzoates to Indeno[1,2- c ]azepines and Azabicyclo[4.2.0]octa-1(8),5-dines
A synthetic method that relies on Au(I)-catalyzed cycloisomerization reactions of 1,7-diyne benzoates to prepare indeno[1,2-c]azepines and azabicyclo[4.2.0]octa-1(8),5-dines is described.
NIAID Data Ecosystem20
Gold-Catalyzed Cycloisomerization of 1,7-Diyne Benzoates to Indeno[1,2-c]azepines and Azabicyclo[4.2.0]octa-1(8),5-dines
A synthetic method that relies on Au(I)-catalyzed cycloisomerization reactions of 1,7-diyne benzoates to prepare indeno[1,2-c]azepines and azabicyclo[4.2.0]octa-1(8),5-dines is described.
Figshare2016-02-20 更新00
Gold-Catalyzed Cycloisomerization of 1,7-Diyne Benzoates to Indeno[1,2- c ]azepines and Azabicyclo[4.2.0]octa-1(8),5-dines
A synthetic method that relies on Au(I)-catalyzed cycloisomerization reactions of 1,7-diyne benzoates to prepare indeno[1,2-c]azepines and azabicyclo[4.2.0]octa-1(8),5-dines is described.
NIAID Data Ecosystem10
Gold-Catalyzed Cycloisomerization of 1,7-Diyne Benzoates to Indeno[1,2- c ]azepines and Azabicyclo[4.2.0]octa-1(8),5-dines
A synthetic method that relies on Au(I)-catalyzed cycloisomerization reactions of 1,7-diyne benzoates to prepare indeno[1,2-c]azepines and azabicyclo[4.2.0]octa-1(8),5-dines is described.
NIAID Data Ecosystem30
