“…The latter contain esterifying acids related to cinnamic acid (14). The 7-monoester 4 which has been previously reported as a constituent of Heliotropium currassavicum (15), may be naturally occurring or could have arisen by partial hydrolysis of 2. EXPERIMENTAL General experimental procedures.-Dccc was carried out using a Biichi 670 DCC chromatograph containing 500 tubes of 2.7 mm i.d.…”
Reinvestigation of Cynoglossum creticum led to the isolation of the previously reported echinatine [1] and heliosupine [2] as well as rinderine [3], 7-angelylheliotridine [4] and a new alkaloid, cynoglossamine [5]. The structures have been determined by spectral means (ir, ms, 1H-13C HETCOR nmr), comparison with literature data and authentic samples, and/or syntheses. In addition, 1 and all three of its isomers 3, 6, and 7 and other semisynthetic analogues (8-13) were prepared and characterized.
“…The latter contain esterifying acids related to cinnamic acid (14). The 7-monoester 4 which has been previously reported as a constituent of Heliotropium currassavicum (15), may be naturally occurring or could have arisen by partial hydrolysis of 2. EXPERIMENTAL General experimental procedures.-Dccc was carried out using a Biichi 670 DCC chromatograph containing 500 tubes of 2.7 mm i.d.…”
Reinvestigation of Cynoglossum creticum led to the isolation of the previously reported echinatine [1] and heliosupine [2] as well as rinderine [3], 7-angelylheliotridine [4] and a new alkaloid, cynoglossamine [5]. The structures have been determined by spectral means (ir, ms, 1H-13C HETCOR nmr), comparison with literature data and authentic samples, and/or syntheses. In addition, 1 and all three of its isomers 3, 6, and 7 and other semisynthetic analogues (8-13) were prepared and characterized.
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