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raptorlane
  • Member for 1 year, 3 months
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4 votes
0 answers
114 views

Hydrolyse a fluorophosphonic compound / Which protective group strategy can I use for phosphonate esters to access the free acid after a reaction?

4 votes
2 answers
234 views

Can glycerol slow down the kinetics of an inhibitor going to a binding pocket of a target enzyme?

4 votes
0 answers
270 views

Exchange of Fluorine to Oxygen for Fluorophosphonic acid by silylating agents or other methods?

4 votes
1 answer
106 views

Compatibility of DCM/CCl3 with sodium hydride

3 votes
1 answer
163 views

Are there LCMS compatible buffer systems available for the high pH range 12-14?

3 votes
0 answers
119 views

Hydrolyse Phosphonate diester to free phosphonic acid under relatively mild conditions?

2 votes
1 answer
88 views

What can I do if a peptide won't go in solution in a biological assay?

2 votes
1 answer
128 views

Calculate IC50 from fluorescence kinetic

2 votes
0 answers
37 views

Synthesize pivaloyloxymethyl ester, but with a substrate that is a terrible nucleophile

2 votes
0 answers
35 views

Electrophilic fluorination power: selectfluor vs NFSI

2 votes
0 answers
32 views

TMSBr and 2,4,6 Collidin in Acetonitrile leads to white precipitate

2 votes
1 answer
60 views

(Di)chlorination of phosphonic acid ester

2 votes
0 answers
56 views

Clean *di* protection of phosphonic acid dichloride with a suitable protection group with clean deprotection

2 votes
0 answers
69 views

Stability of n-Dodecyl-beta-D-maltoside in buffer solutions for assay experiments

1 vote
1 answer
125 views

Making an UV inactive salt UV active during purification of charged anion with HILIC purification?

1 vote
0 answers
51 views

Transesterfication: Which is a suitable acid that does not contaminate the polar product?

1 vote
0 answers
146 views

Are there TLC stains for organo fluor compounds or anorg. fluoride that are useful for selecting the product containing fractions post purification

1 vote
0 answers
299 views

What is a suitable process to eliminate an excess of pyridine from an aqueous solution?

1 vote
0 answers
33 views

Avoid triethylphosphate as a side product during P-C-P coupling reaction with diethylchlorophosphate with LDA

1 vote
0 answers
45 views

Esterification of phosphonic acid chloride is working with isoprenol but not with prenol

1 vote
0 answers
56 views

TMSiBr and Oxalylchloride for ester cleavage

0 votes
0 answers
62 views

Elegant and fast way without chromatography to remove fluoride ions from water phase without contamination of the polar water soluble product?