Organic Letters, volume 15, issue 16, pages 4174-4177
Development of a Practical, Asymmetric Synthesis of the Hepatitis C Virus Protease Inhibitor MK-5172
Jeffrey Kuethe
1
,
Yongli Zhong
1
,
Nobuyoshi Yasuda
1
,
Gregory L Beutner
1
,
Katherine Linn
1
,
Mary Kim
1
,
Benjamin Marcune
1
,
Spencer D. Dreher
1
,
Guy R Humphrey
1
,
Tao Pei
1
1
Process Chemistry, Merck Research Laboratories, P.O. Box 2000, Rahway, New Jersey 07065-0200, United States
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Publication type: Journal Article
Publication date: 2013-08-06
Journal:
Organic Letters
scimago Q1
SJR: 1.245
CiteScore: 9.3
Impact factor: 4.9
ISSN: 15237060, 15237052
PubMed ID:
23919347
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Abstract
The development of a practical, asymmetric synthesis of the hepatitis C virus (HCV) protease inhibitor MK-5172 (1), an 18-membered macrocycle, is described.
Found
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