Butylboronic acid N,N,N′,N′-tetramethyl-L-tartaric acid diamide ester (CAS 161344-85-0)
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Butylboronic acid N,N,N′,N′-tetramethyl-L-tartaric acid diamide ester is frequently employed in the field of organic chemistry, particularly in asymmetric synthesis where it acts as a chiral auxiliary or catalyst. Its structure allows for the stabilization of transition states, thus facilitating the formation of enantiomerically enriched compounds. In research on new synthetic pathways, this compound is of interest for its ability to impart stereoselectivity in reactions such as Suzuki couplings. Moreover, it supports the study of boron-containing compounds′ reactivity and their potential interactions with various organic substrates. The compound also finds application in material sciences, where researchers investigate its role in the formation of polymers with specific optical properties.
Butylboronic acid N,N,N′,N′-tetramethyl-L-tartaric acid diamide ester (CAS 161344-85-0) References
- Total synthesis of (+)-frondosin A. Application of the Ru-catalyzed [5+2] cycloaddition. | Trost, BM., et al. 2007. J Am Chem Soc. 129: 11781-90. PMID: 17760442
- Coibacins A and B: total synthesis and stereochemical revision. | Carneiro, VM., et al. 2014. J Org Chem. 79: 630-42. PMID: 24359482
- Stereoselective Synthesis of (S)- and (N)-Cyclopropyl-Fused Carbocyclic Nucleosides Using Stereoselective Cyclopropanation. | Hyun, YE., et al. 2021. J Org Chem. 86: 9828-9837. PMID: 34184528
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Butylboronic acid N,N,N′,N′-tetramethyl-L-tartaric acid diamide ester, 5 g | sc-227551 | 5 g | $275.00 |