[ 3 / biz / cgl / ck / diy / fa / ic / jp / lit / sci / vr / vt ] [ index / top / reports ] [ become a patron ] [ status ]
2023-11: Warosu is now out of extended maintenance.

/sci/ - Science & Math

View post   
File: 156 KB, 2137x925, Screenshot_9.png [View same] [iqdb] [saucenao] [google]
12058674 No.12058674 [Reply] [Original]

This is the state of chemistry journals in 2020

>> No.12059223

>>12058674
>citations: zero
It'll stay that way.

>> No.12059290

>>12059223
Not unthinkable for those retards to cross-reference themselves.

>> No.12059381

>>12059223
It was published Aug 10, papers aren't generally going through review in 18 days. Someone might be writing something relevant and be at the resubmission with revisions stage when this was published, but the number of papers on that subject in that time frame has got to be tiny.

>> No.12060339
File: 11 KB, 253x111, unfavorable homo-homo interaction.png [View same] [iqdb] [saucenao] [google]
12060339

Can we talk chemistry here? I don't know of any imageboards which do and my questions are too dumb for Stack Exchange.

Anyone got good suggestions for 1,2-imino ketals? The most simple route I have in mind is start with a 1,2-diketone, monoketalize it then condense it with an amine using a water-removing method. It's 3 steps, but highly clickable. I think a quicker route would be to simply oxidate an 1,2-amino alcohol, but I haven't found any reactions proven to oxidate both functions.

>> No.12060778

>>12060339
>proven to oxidate both functions.
Wouldn't you only need to oxidize one?

>> No.12060968

>>12060778
Gotta turn the amine into imine and the hydroxyl into carbonyl, so I can protect the latter with a ketal. I suppose I could oxidize the amino alcohol once to get the amino ketone, ketalize it and then oxidize the amine, but this route seems pointless if I can oxidize both in one step.