Traxler P, Fritz H, Fuhrer H, Richter W J
J Antibiot (Tokyo). 1980 Sep;33(9):967-78. doi: 10.7164/antibiotics.33.967.
The structures of the papulacandins A, B, C and D, new antibiotics of Papularia sphaerosperma have been established by means of spectral analysis and degradation reactions. Base catalysed hydrolysis of the main product papulacandin B (1) gave two new hydroxylated long-chain unsaturated fatty acids 5 and 6 along with a hitherto unknown spirocyclic diglycoside 7. The structure of 7 was determined by further degradation reactions. The positions of attachment of the two fatty acids to the spirocyclic diglycoside 7 through ester-bonds were established by selective base catalysed hydrolysis of 1 and spectral analysis of 1 and some derivatives and degradation products thereof. The structures of papulacandin A (2), papulacandin C (3) and papulacandin D (4) were determined in an analogous way.
通过光谱分析和降解反应确定了球形孢囊霉新抗生素——丘疹霉素A、B、C和D的结构。主要产物丘疹霉素B(1)在碱催化下水解,得到两种新的羟基化长链不饱和脂肪酸5和6,以及一种迄今未知的螺环二糖苷7。通过进一步的降解反应确定了7的结构。通过对1进行选择性碱催化水解以及对1及其一些衍生物和降解产物进行光谱分析,确定了两种脂肪酸通过酯键连接到螺环二糖苷7上的位置。以类似的方式确定了丘疹霉素A(2)、丘疹霉素C(3)和丘疹霉素D(4)的结构。