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A steroidal cyclopeptide, synthesis and shape of the cavity

✍ Scribed by Dieter Albert; Martin Feigel


Publisher
Elsevier Science
Year
1994
Tongue
French
Weight
318 KB
Volume
35
Category
Article
ISSN
0040-4039

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✦ Synopsis


Abr#ract: Cycle-[3a-(pbcoylalaninylamino)-5g-cbolanate]s 2 was synthesized from litbocbolic acid and (S)-pbenylalanioe, Tbe synthesis requires three transformations: i) stereoselective convcrsioo of the 3a-bydroxy group to the fa-amino group; ii) preparation of the linear steroidal peptide; iii) cyclodimerisatioo.

NMR measurements and MM3 calculations support a conformation of 2 with a lipophilic cavity.


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