Preparation of Some Derivatives of N‐tert‐Butyldecahydro‐3‐isoquinoline Carboxamide

References

• Squire , M. D. , Davis , R. A. , Chianakas , K. A. , Ferrence , G. M. , Standard , J. M. and Hitchcock , S. R. 2005 . Synthesis, X‐ray crystallography and computational studies concerning an oxadiazinone derived from D‐camphor: A structural limitation of oxadiazinones as chiral auxiliaries . Tetrahedron: Asymmetry , 16 : 1047 – 1053 .
   Google Scholar
• Hitchcock , S. R. , Casper , D. M. , Vaughn , J. F. , Finefield , J. M. , Ferrence , G. M. and Esken , J. M. 2004 . Intramolecular chiral relay at stereogenic nitrogen: Synthesis and application of a new chiral auxiliary derived from (1R,2S)‐norephedrine and acetone . J. Org. Chem. , 69 : 714 – 718 .
   PubMed Web of Science ®Google Scholar
• Casper , D. M. and Hitchcock , S. R. 2003 . An improved procedure for the asymmetric aldol reaction of the titanium enolate of an N3‐propionyl‐3,4,5,6‐tetrahydro‐2H‐1,3,4‐oxadiazin‐2‐one . Tetrahedron: Asymmetry , 14 : 517 – 521 .
   Google Scholar
• Albizati , K. F. , Babu , S. , Birchler , A. , Busse , J. K. , Fugett , M. , Grubbs , A. , Haddach , A. , Pagan , M. , Potts , B. , Remarchuk , T. , Rieger , D. , Rodriguez , R. , Shanley , J. , Szendroi , R. , Tibbetts , T. , Whitten , K. and Borer , B. 2001 . A synthesis of the HIV‐protease inhibitor nelfinavir from D‐tartaric acid . Tetrahedron Lett. , 42 : 6481 – 6485 .
   Web of Science ®Google Scholar
• Zook , S. E. , Busse , J. K. and Borer , B. C. 2000 . A concise synthesis of the HIV‐protease inhibitor nelfinavir via an unusual tetrahydrofuran rearrangement . Tetrahedron Lett. , 41 : 7017 – 7021 .
   Web of Science ®Google Scholar
• Inaba , T. , Birchler , A. G. , Yamada , Y. , Sagawa , S. , Yokota , K. , Ando , K. and Uchida , I. 1998 . A practical synthesis of nelfinavir, an HIV‐protease inhibitor, using a novel chiral C4 building block: (5R,6S)‐2,2‐Dimethyl‐5‐hydroxy‐1,3‐dioxepan‐6‐ylammonium acetate . J. Org. Chem. , 63 : 7582 – 7583 .
   Web of Science ®Google Scholar
• Kaldor , S. W. , Kalish , V. J. , Davies , J. F. II , Shetty , B. V. , Fritz , J. E. , Appelt , K. , Burgess , J. A. , Campanale , K. M. , Chirgadze , N. Y. , Clawson , D. K. , Dressman , B. A. , Hatch , S. D. , Khalil , D. A. , Kosa , M. B. , Lubbehusen , P. P. , Muesing , M. A. , Patrick , A. K. , Reich , S. H. , Su , K. S. and Tatlock , J. H. 1997 . Viracept (nelfinavir mesylate, AG1343): A potent, orally bioavailable inhibitor of HIV‐1 protease . J. Med. Chem. , 40 : 3979 – 3985 .
   PubMed Web of Science ®Google Scholar
• Ghosh , A. K. , Hussain , K. A. and Fidanze , S. 1997 . Asymmetric aldol route to hydroxyethylamine isostere: Stereoselective synthesis of the core unit of saquinavir . J. Org. Chem. , 62 : 6080 – 6082 .
   PubMed Web of Science ®Google Scholar
• Dondoni , A. , Perrone , D. and Merino , P. 1995 . Chelation‐ and non‐chelation‐controlled addition of 2‐(trimethylsilyl)thiazole to alpha‐amino aldehydes: Stereoselective synthesis of the beta‐amino‐alpha‐hydroxy aldehyde intermediate for the preparation of the human immunodeficiency virus proteinase inhibitor Ro 31‐8959 . J. Org. Chem. , 60 : 8074 – 8080 .
   Google Scholar
• Parkes , K. E. B. , Bushnell , D. J. , Crackett , P. H. , Dunsdon , S. J. , Freeman , A. C. , Gunn , M. P. , Hopkins , R. A. , Lambert , R. W. , Martin , J. A. , Merrett , J. H. , Redshaw , S. , Spurden , W. C. and Thomas , G. J. 1994 . Studies toward the large‐scale synthesis of the HIV proteinase inhibitor Ro 31‐8959 . J. Org. Chem. , 59 : 3656 – 3664 .
   Web of Science ®Google Scholar
• Becker , H. and Sharpless , K. B. 2001 . Asymmetric Oxidation Reactions Edited by: Katsuki , T. 81 – 104 . Oxford, , UK : Oxford University Press .
   Google Scholar
• Niwa , H. , Hida , T. and Yamada , K. 1981 . A new method for cleavage of aliphatic methyl ethers . Tetrahedron Lett. , 22 : 4239 – 4240 .
   Web of Science ®Google Scholar