U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Synthesis of sialosides

Patent 5138044 Issued on August 11, 1992. Estimated Expiration Date: Icon_subject August 13, 2010. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

Sialic acid derivative and process for preparing the same
Patent #: 4691012
Issued on: 09/01/1987
Inventor: Ogura ,   et al.

Sialic acid derivatives
Patent #: 4694076
Issued on: 09/15/1987
Inventor: Ogawa ,   et al.

Process for producing sialic acid derivatives
Patent #: 4914035
Issued on: 04/03/1990
Inventor: Hasegawa, et al.

3-phenylthiosialic acid derivative, sialic acid-containing oligosaccharide derivative and process for preparing these compounds Patent #: 4935506
Issued on: 06/19/1990
Inventor: Goto, et al.

Inventor

Assignee

Application

No. 566682 filed on 08/13/1990

US Classes:

536/18.5, Processes536/4.1, O- or S- Glycosides536/17.1, Boron, phosphorus, heavy metal or aluminum containing536/17.5, Sulfur containing (e.g., methylthiolincosaminide, etc.)536/54, Sulfur containing536/55.2, Glucosamine containing536/55.3Processes

Examiners

Primary: Brown, Johnnie R.
Assistant: White, Everett

Attorney, Agent or Firm

Foreign Patent References

  • 346814 EP 12/13/1989
  • 61-282390 JP 12/13/1986
  • 63-41494 JP 02/13/1988
  • 64-52794 JP 02/13/1989

International Classes

C07G 003/00
C07H 005/04
C07H 005/10

Abstract

Reaction schemes for carrying out a variety of chemical synthesis are disclosed. The reactions produce ଱-(X)-sialosides wherein X is O, S, N or another compatible electron donating atom or molecular moiety. The reaction schemes include a relatively small number of steps to provide a yield with a relatively small amount of undesired ଲ-configuration product. Compounds synthesized are encompassed by the following general structural formula I. ##STR1## wherein R, R' and R" are each independently H, CH3, acetyl, or a disaccharide which is preferably lactose.

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