Studies toward the large-scale synthesis of the HIV proteinase inhibitor Ro 31-8959

KEB Parkes, DJ Bushnell, PH Crackett…

Index: Journal of Organic Chemistry, , vol. 59, # 13 p. 3656 - 3664

Full Text: HTML

Citation Number: 124

Abstract

... (14) Maibaum, J.; Rich, DH J . Org. Chem. ... The tris- ((trimethylsily1)oxy)ethene chemistry developed by Wiss- ner for the preparation of a-hydroxymethyl ketones from acid chlorides offered a potentially attractive method of preparing a homophenylalanine synthon of the sort ...

Related Articles:

Studies toward the large-scale synthesis of the HIV proteinase inhibitor Ro 31-8959

[Parkes, Kevin E. B.; Bushnell, David J.; Crackett, Peter H.; Dunsdon, Stephen J.; Freeman, Andrew C.; et al. Journal of Organic Chemistry, 1994 , vol. 59, # 13 p. 3656 - 3664]

Reduction of peptide character of HIV protease inhibitors that exhibit nanomolar potency against multidrug resistant HIV-1 strains

[Journal of Medicinal Chemistry, , vol. 46, # 9 p. 1764 - 1768]

Studies toward the large-scale synthesis of the HIV proteinase inhibitor Ro 31-8959

[Parkes, Kevin E. B.; Bushnell, David J.; Crackett, Peter H.; Dunsdon, Stephen J.; Freeman, Andrew C.; et al. Journal of Organic Chemistry, 1994 , vol. 59, # 13 p. 3656 - 3664]

The development of cyclic sulfolanes as novel and high-affinity P2 ligands for HIV-1 protease inhibitors

[Journal of Medicinal Chemistry, , vol. 37, # 8 p. 1177 - 1188]

Studies toward the large-scale synthesis of the HIV proteinase inhibitor Ro 31-8959

[Parkes, Kevin E. B.; Bushnell, David J.; Crackett, Peter H.; Dunsdon, Stephen J.; Freeman, Andrew C.; et al. Journal of Organic Chemistry, 1994 , vol. 59, # 13 p. 3656 - 3664]

More Articles...