Carbamate derived stable precursors for generating chiral azomethine ylids under mild conditions
-
Add time:09/08/2019 Source:sciencedirect.com
We describe the evolution of stable azomethine ylid precursors which avoid the need for an aldehyde in the ylid generation step. tert-Butyl carbamate derivative (16) demonstrates comparable efficiency to the standard method of ylid generation and trapping, but permits use of milder conditions.
We also recommend Trading Suppliers and Manufacturers of ethyl (hydroxymethyl)(methoxymethyl)carbamate (cas 13057-81-3). Pls Click Website Link as below: cas 13057-81-3 suppliers
Prev:Surface modification of vulcanized styrene–butadiene rubber with triChloroisocyanuric Acid (cas 13057-78-8) solutions of different active chlorine contents
Next:A preliminary investigation of the toxic effects of benzylpenicilloic acid (cas 13057-98-2)) - 【Back】【Close 】【Print】【Add to favorite 】
-
Health and Chemical more >
-
Related Products
- Ethyl (13-cis)-9-(4-methoxy-2,3,6-trimethylphenyl)-3,7-dimethyl-2,4,6,8-nonatetraenoate
- ethyl (1R,2R)-1-phenyl-2-(trideuteriomethylamino)cyclohex-3-ene-1-carboxylate,hydrochloride
- Ethyl (1S,2R)-2-(dimethylamino)-1-phenylcyclohex-3-ene-1-carboxylate hydrochloride
- Ethyl (2,4,6-trimethylbenzoyl) phenylphosphinate
- Ethyl (2-amino-4-hydroxy-6-methyl-5-pyrimidinyl)acetate
- Ethyl (2-bromopropionamido)acetate
- Ethyl (2-cyanoimino-5,6-dichloro-1,2,3,4-tetrahydroquinazolin-3-yl)acetate
- ETHYL (2E,4Z)-DECADIENOATE
- Ethyl (2-hydroxyethyl)dimethyl-ammonium benzilate chloride
- Ethyl (2-mercaptoethyl) carbamate S-ester with O,O-dimethyl phosphorodithioate