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1. J. Amer. Chem. Soc. 1968. 90: 6254-6255.
Corey E. J., Ortiz de Montellano P. R., Yamamoto H.
Separation of the cyclization and rearrangement processes of sterol biosynthesis. Enzymic formation of a protosterol derivative.
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dx.doi.org/10.1021/ja01024a076Corey E. J., Virgil S. C.
Enantioselective total synthesis of a protosterol, 3β,20-dihydroxyprotost-24-ene.
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dx.doi.org/10.1021/ja00173a059Mitsuguchi H., Seshime Y., Fujii I., Shibuya M., Ebizuka Y., Kushiro T.
Biosynthesis of steroidal antibiotic fusidanes: functional analysis of oxidosqualene cyclase and subsequent tailoring enzymes from Aspergillus fumigatus.
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dx.doi.org/10.1021/ja8095976O’Grodnick J. S., Ebersole R. C., Wittstruck T., Caspi E.
Trans dehydration of alcohols with methyl (carboxysulfamoyl)triethylammonium hydroxide inner salt.
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dx.doi.org/10.1021/jo00928a037Marsault E., Deslongchamps P.
Increasing the efficiency of the transannular Diels-Alder strategy via stille macrocyclizations.
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dx.doi.org/10.1021/ol000209h