+ Site Statistics
References:
54,258,434
Abstracts:
29,560,870
PMIDs:
28,072,757
+ Search Articles
+ Subscribe to Site Feeds
Most Shared
PDF Full Text
+ PDF Full Text
Request PDF Full Text
+ Follow Us
Follow on Facebook
Follow on Twitter
Follow on LinkedIn
+ Translate
+ Recently Requested

Selective functionalization of s tyrosine development of a highly efficient synthesis of fibrinogen receptor antagonist l 700462



Selective functionalization of s tyrosine development of a highly efficient synthesis of fibrinogen receptor antagonist l 700462



Abstracts of Papers American Chemical Society 204(1-2): ORGN 271




(PDF emailed within 1 workday: $29.90)

Accession: 033331608

Download citation: RISBibTeXText


Related references

A practical synthesis of fibrinogen receptor antagonist MK-383: Selective functionalization of (S)-tyrosine. Tetrahedron 49(26): 5767-5776, 1993

A highly efficient synthesis of fibrinogen receptor antagonist L-734,217 via a novel chemoselective silyl-mediated conjugate addition of delta-lactams to 4-vinylpyridine. Abstracts of Papers American Chemical Society 211(1-2): ORGN 227, 1996

Activity and safety of L-700462, a selective GPIIb/IIIa antagonist, in healthy volunteers. Circulation 86(4 SUPPL 1): I866, 1992

Efficient Synthesis Of A Selective Y5 Receptor Antagonist. Synthetic Communications 32(11): 1715-1719, 2002

Efficient ArndtEistert Synthesis of Selective 5-Ht 7 Receptor Antagonist Sb-269970. Synthetic Communications 39(18): 3243-3253, 2009

A highly efficient synthesis of RWJ 47639: A novel, orally active angiotensin II receptor antagonist. Bioorganic and Medicinal Chemistry Letters 3(8): 1523-1526, 1993

Development of novel highly selective fibrinogen receptor antagonists as potentially useful antithrombotic agents. Smith, J A And J E Rivier (Ed ) Peptides: Chemistry And Biology; Twelfth American Peptide Symposium, Cambridge, Massachusetts, Usa, June 16-21, 1991 Lviii+989p Escom Science Publishers B V : Leiden, Netherlands Illus 914-916, 1992

Non-peptide fibrinogen receptor antagonists. 7. Design and synthesis of a potent, orally active fibrinogen receptor antagonist. Journal of Medicinal Chemistry 38(17): 3332-3341, 1995

Total synthesis of SR 121463 A, a highly potent and selective vasopressin v(2) receptor antagonist. Journal of Organic Chemistry 66(11): 3653-3661, 2001

Efficient asymmetric synthesis of novel gastrin receptor antagonist AG-041R via highly stereoselective alkylation of oxindole enolates. Journal of Organic Chemistry 71(22): 8559-8564, 2006

Synthesis of highly selective and potent non peptide delta opioid receptor antagonist naltrindole. Zhongguo Yiyao Gongye Zazhi 21(3): 101-102, 1990

Discovery, Synthesis, and Structure Activity of a Highly Selective a7 Nicotinic Acetylcholine Receptor Antagonist. Biochemistry (American Chemical Society) 46(22): 28-38, 2007

Radical arylation of tyrosine and its application in the synthesis of a highly selective neurotensin receptor 2 ligand. Organic and Biomolecular Chemistry 9(10): 3746-3752, 2011

Discovery, synthesis, and structure activity of a highly selective alpha7 nicotinic acetylcholine receptor antagonist. Biochemistry 46(22): 6628-6638, 2007

A highly stereoselective Michael addition to an alpha,beta-unsaturated ester as the crucial step in the synthesis of a novel beta-amino acid-containing fibrinogen receptor antagonist. Journal of Organic Chemistry 58(27): 7948-7951, 1993