Molecular Biology

The enantiodiscrimination of (1 R )-(+)-(1-amino-2-methylpropyl)phosphonic acid from its enantiomer in the gas-phase can be done using ESI-MS-CID technique. [electrospray ionization-mass spectrometric detection-collision induced dissociation]

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Application Used to prepare chiral double allylation reagents.

Application Used to prepare chiral double allylation reagents.

Analysis Note Assay (GC, area%): &#8805 96.0 % (a/a) Spec.

Analysis Note Assay (GC, area%): &#8805 96.0 % (a/a) Spec.

Analysis Note Assay (GC, area%): &#8805 96.0 % (a/a) Spec.

Application (2 R ,3 R )-iPr-BIDIME is a P-chiral monophosphorus ligand used for the transition metal-catalyzed asymmetric Suzuki-Miyaura and hydroboration reactions. Other Notes Synthesis of Chiral &#945-Amino Tertiary Boronic Esters by

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Application (2 R )-(-)-Glycidyl tosylate may be used to prepare: 1- O -hexadecyl-sn-glycerol 3- O - p -toluenesulfonate by reacting with 1-hexadecanol in the presence of boron trifluoride etherate. 4-Oxiranylmethoxy-(1 H )-indole by reacting with

Application (2 R )-(-)-Glycidyl tosylate may be used to prepare: 1- O -hexadecyl-sn-glycerol 3- O - p -toluenesulfonate by reacting with 1-hexadecanol in the presence of boron trifluoride etherate. 4-Oxiranylmethoxy-(1 H )-indole by reacting with

Application Used in the first enantioselective synthesis of ( R )- and ( S )-4-acetyl-3-(hydroxymethyl)-3,4-dihydro-2 H -pyrido[3,2- b ]oxazines. Legal Information Manufactured under license by Sterling Pharma Solutions Limited, using Jacobsen HKR