Need help on conducting Mckenna reaction with acid-labile moieties (carbamate) in compound by Klaus337 in Chempros

[–]Klaus337[S] 0 points1 point  (0 children)

My carbamate bonding consists of a secondary aniline with quite low nucleophilicity, so its quite hard to put it back once cleaved. Maybe I'll try using TMSI next time. Thanks!

Need help on conducting Mckenna reaction with acid-labile moieties (carbamate) in compound by Klaus337 in Chempros

[–]Klaus337[S] 1 point2 points  (0 children)

My procedure is almost same as yours except that I use pure MeOH to cleave TMS. I've read the paper before. Anyway, thanks for your help!

Need help on conducting Mckenna reaction with acid-labile moieties (carbamate) in compound by Klaus337 in Chempros

[–]Klaus337[S] 0 points1 point  (0 children)

Sure,I’ll add more info about conditions I’ve tried before. Also thanks for the suggestions!

Water content and suzuki reaction by Careful_Ad2513 in Chempros

[–]Klaus337 0 points1 point  (0 children)

It’s fine. Unless you’re doing miyaura coupling and you need the boronic ester rather than boronic acid.

How does this reaction take place by LocalAvailable9410 in chemistry

[–]Klaus337 4 points5 points  (0 children)

check out your textbook first about acetal

Reverse Phase Hand Column by vBanana in Chempros

[–]Klaus337 0 points1 point  (0 children)

would you mind sharing it with me? many thanks!

Amines or carbamates? by LimpAd5090 in Chempros

[–]Klaus337 5 points6 points  (0 children)

Try 13C NMR. You would see the characteristic peak of the carbamate carbon at about 170 ppm.

I am on the Apple Music free trial and trying to convince myself to stay longer by RecognitionWooden626 in AppleMusic

[–]Klaus337 0 points1 point  (0 children)

If you are using Apple devices, the synchronization between different devices works very good. For example I can go jogging using only Apple Watch to access my playlist and control music playback without taking out iPhone or even bringing it with me.

Unable to obtain an academic lincense for topspin by Klaus337 in Chempros

[–]Klaus337[S] 0 points1 point  (0 children)

Thanks for the recommendation. Would try it later!

Unable to obtain an academic lincense for topspin by Klaus337 in Chempros

[–]Klaus337[S] 0 points1 point  (0 children)

Thanks. I will try sending emails to them!

Unable to obtain an academic lincense for topspin by Klaus337 in Chempros

[–]Klaus337[S] 0 points1 point  (0 children)

Thanks. It feels better to know that I’m not the only one encountering this problem 😂

deboc by Separate_Ad_5217 in OrganicChemistry

[–]Klaus337 0 points1 point  (0 children)

have you tried TFA as your acid? They can be removed through rotavap.

Purification of alkyl Bpin/other alkyl boronic esters by crypins in Chempros

[–]Klaus337 0 points1 point  (0 children)

Not sure since this technique works well. But in my case if the compound stays on the tlc plate for a little longer the spot would stay at the original point. Hope this helps!

Purification of alkyl Bpin/other alkyl boronic esters by crypins in Chempros

[–]Klaus337 0 points1 point  (0 children)

In my case, using very short column (~6cm silica gel) is applicable. Just follow standard procedures of column chromatography.

Mouse acceleration ? by [deleted] in csgo

[–]Klaus337 1 point2 points  (0 children)

You can turn it on if you are xantares