- been used in a
number of syntheses,
including macrosphelides A and B,
amphidinolide J, and
spirofungins A and B.
Weinreb and Nahm
originally proposed the...
- An
elegant example of
Negishi coupling is Furstner's
synthesis of
amphidinolide T1: ****uyama
coupling is a palladium-catalyzed
reaction involving the...
-
Ostreopsis siamensis Dinophyceae Linear polyether Na+/K+
ATPase disruptor Amphidinolide,
Caribenolide Amphidinium spp.
Dinophyceae Macrocyclic polyether Cytotoxic...
- 1449–1470. doi:10.1021/cr00020a004. Trost, BM; et al. (2005). "Synthesis of
Amphidinolide P". J. Am. Chem. Soc. 127 (50): 17921–17937. doi:10.1021/ja055967n....
- From
Total Synthesis to
Diverted Total Synthesis: Case
Studies in the
Amphidinolide Series. Isr. J. Chem., 51: 329–345. doi:10.1002/ijch.201100006 Counting...
- Ragot, Jacques; Fürstner,
Alois (December 2003). "Total
Syntheses of
Amphidinolide T1, T3, T4, and T5".
Journal of the
American Chemical Society. 125 (50):...
-
Figadere used the Liebeskind–Srogl
coupling early in
their synthesis of
amphidinolide F by
employing this
reaction to
construct the
north eastern fragment...
- TBDPS-, and TBS-Substituted
Alkenes in
Connection with the
Synthesis of
Amphidinolides B/D".
Organic Letters. 13 (18): 4934–4937. doi:10.1021/ol2020187. ISSN 1523-7060...
-
entities based on sugar,
Amino Acids and
anticancer compounds such as
amphidinolides, epothilones, crocacins, and
clavosolide and the
synthesis of glycopeptide...
