MM 47755

[ Density]:
1.39g/cm3

[ Boiling Point ]:
583.3ºC at 760mmHg

[ Molecular Formula ]:
C₂₀H₁₆O₅

[ Molecular Weight ]:
336.33800

[ Flash Point ]:
214.3ºC

[ Exact Mass ]:
336.10000

[ PSA ]:
80.67000

[ LogP ]:
2.35050

[ Vapour Pressure ]:
1.89E-14mmHg at 25°C

[ Index of Refraction ]:
1.652

[ Symbol ]:

GHS07, GHS09

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H410

[ Precautionary Statements ]:
P273-P501

[ RIDADR ]:
UN 3077 9 / PGIII

Angucyclinone antibiotics: total syntheses of YM-181741, (+)-ochromycinone, (+)-rubiginone B2, (-)-tetrangomycin, and MM-47755.

J. Org. Chem. 72(16) , 6116-26, (2007)

A concise and highly enantioselective route has been developed for the synthesis of angucyclinone-type natural products. Utilizing this strategy, total syntheses of five natural products YM-181741, (+...

Total synthesis of (-)-8-O-methyltetrangomycin (MM 47755).

Org. Lett. 8(12) , 2507-10, (2006)

A stereoselective total synthesis of the natural antibiotic (-)-8-O-methyltetrangomycin 1 is reported. The essential steps for this convergent synthesis are the transformation of a geraniol epoxide in...

The cobalt way to angucyclinones: asymmetric total synthesis of the antibiotics (+)-rubiginone B2, (-)-tetrangomycin, and (-)-8-O-methyltetrangomycin.

Chemistry 16(29) , 8805-21, (2010)

A cobalt(I)-mediated convergent and asymmetric total synthesis of angucyclinones with an aromatic B ring has been developed. In the course of our research, we synthesized three naturally occurring ang...

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