摘要:
The prevalence of a C - common core in diverse C terpenes has been recognised. A bifun%onal C I 2-cyclopentanoid deriva%:% corresponding to this common-core has been prepared from R-(+)-limonene. The enantio- merically pure 2 has been elaborated to several sesqui- and diterpene skeleta. In particular, enantioselective syntheses of isodaucane sesquiterpene, (+)-apha- namol-I, 3 aand dolabellane diterpene, 6-araneosene 26 have been accom- plished for the first time. A general solution to the stereochemical problem associated with this class of compounds has been devised. Syntheses of (-)- daucene 8 and (+)-isoamijiol 17a r e also described.
摘要:
Aza-Claisen rearrangement of N-2 (E)-butenyl-N-butylpropanamide was found
to proceed smoothly at’v135OC in the presence of LDA to furnish syn-N-
butyl-2,3-dimethyl-4-pentenamidein- 948 yield and >99% de. The reaction
with the corresponding N-(lS)-l-phenethyl derivative yielded (2R, 3s)-N-
[(lS)-1-phenethyl) -2,3-dimethyl-4-pentenamidein 83% de. An efficient
and generally-applicable two-step procedure for the hydrolysis of N-mono-
substituted amides was also developed and the corresponding carboxylic
acids were obtained in good yields without any epimerization at thea-
position of the acyl group. The amines used for the chiral induction can
be recovered in 71% yield.