跳转至内容

Dear Customer:

The current international situation is complex and volatile, and uncertain tariff policies may potentially impact our product prices. Given these uncertainties, we value your understanding regarding order-related matters.

If you decide to place an order during this period, we reserve the right to adjust the price based on the evolving situation. We understand that market changes may cause inconvenience. We will negotiate with you if there’s a significant price fluctuation due to tariff policy changes before the order’s actual delivery, and in such cases we may adjust or cancel the order as necessary.

For important updates on recent policy changes, please click here for more details.

Merck
CN
HomeProfessor Product PortalSheppard Group – Prof. Product Portal

Sheppard Group – Prof. Product Portal

Professor David Nicewicz

Professor Tom Sheppard

Our laboratory is interested in the development of new synthetic methodology and its application to the synthesis of potentially useful molecules. Our research work is spread across a wide range of different areas including transition-metal catalysis (gold, palladium), organoboron chemistry, organocatalysis, multicomponent reactions, and sustainable chemistry.

A common theme in many of the ongoing research projects is the development of new methods for activation or formation of carbon-oxygen bonds. Within this class of reactions, the direct synthesis of amides from carboxylic acids and amines is one of the most important and commonly used reactions in organic chemistry. In our laboratory, we have reported the use of simple borate esters for the direct catalytic formation of amides from a wide variety of carboxylic acids and amines. In particular, B(OCH2CF3)3 is highly effective, and can be used for coupling pharmaceutically relevant substrates containing heterocycles and other functional groups. It can even be employed for the catalytic direct amidation of unprotected amino acids. In most cases, the amide products can be purified using a simple solid-phase work-up with acidic, basic and boron-scavenger resins without the need for an aqueous work-up or chromatography. The reactions are readily scalable to obtain multigram quantities of material, and are considerably more efficient than most other amidation methods (PMI as low as 5 for the synthesis of an amine on 20 g scale).

Other recent work in the group has included the development of a range of catalytic transformations of propargylic alcohols, largely using the PPh3AuNTf2 catalyst originally developed by Fabian Gagosz. Efficient methods have been developed for the gold-catalyzed conversion of these readily available starting materials into enones, 3-alkoxyfurans and dihalohydroxyketones; direct substitution of the propargyl alcohol with a variety of nucleophiles can also be achieved using either a silver catalyst or a simple Brønsted acid.

Sheppard Group Website

Recent papers from the Sheppard Group

1.
Sabatini MT, Boulton LT, Sheppard TD. 2017. Borate esters: Simple catalysts for the sustainable synthesis of complex amides. Sci. Adv.. 3(9):e1701028. https://doi.org/10.1126/sciadv.1701028
2.
Arkhipenko S, Sabatini MT, Batsanov AS, Karaluka V, Sheppard TD, Rzepa HS, Whiting A. Mechanistic insights into boron-catalysed direct amidation reactions. Chem. Sci.. 9(4):1058-1072. https://doi.org/10.1039/c7sc03595k
3.
Foster RW, Tame CJ, Bu?ar D, Hailes HC, Sheppard TD. 2015. Sustainable Synthesis of Chiral Tetrahydrofurans through the Selective Dehydration of Pentoses. Chem. Eur. J.. 21(45):15947-15950. https://doi.org/10.1002/chem.201503510

DISCIPLINES

  • Organic Synthetic Chemistry
  • Chemical Biology

Professor Product Portal Index

登录以继续。

如要继续阅读,请登录或创建帐户。

暂无帐户?