roflamycoin

roflamycoin Suppliers list
Company Name: BOC Sciences
Tel: 16314854226; +16314854226
Email: inquiry@bocsci.com
Products Intro: Product Name:Flavomycoin
CAS:77814-07-4
Remarks:BOC Sciences also provides custom synthesis services for Flavomycoin.
Company Name: Zhejiang Huida Biotech Co., LTD  
Tel: 0571-89903882 13626641628
Email: jiangnan@huidabiotech.com
Products Intro: Product Name:Flavomycoin
CAS:77814-07-4
Purity:99% HPLC Package:10mg;100mg;1g;10g;100g
Company Name: Zhejiang Huida Biotech Co., LTD  
Tel: 0571-0571-89903882 15990081639
Email: sunshixuan@huidabiotech.com
Products Intro: Product Name:Flavomycoin
CAS:77814-07-4
Purity:99% HPLC Package:10mg;100mg;1g;10g;100g
roflamycoin Basic information
Product Name:roflamycoin
Synonyms:14,37-Dioxabicyclo[31.3.1]heptatriaconta-3,5,7,9,11-pentaen-13-one, 19,21,23,25,27,29,31,33,35-nonahydroxy-12,16-dimethyl-15-(1-methylethyl)-, (1R,3E,5E,7E,9E,11E,15S,16S,19S,21S,23S,25R,27R,29S,31R,33S,35S)- (9CI);Roflamycoin
CAS:77814-07-4
MF:C40H66O12
MW:738.94
EINECS:
Product Categories:
Mol File:77814-07-4.mol
roflamycoin Structure
roflamycoin Chemical Properties
Boiling point 972.8±65.0 °C(Predicted)
density 1.154±0.06 g/cm3(Predicted)
pka12.67±0.70(Predicted)
Safety Information
MSDS Information
roflamycoin Usage And Synthesis
SynthesisFor Rychnovsky and co-worker’s synthesis of roflamycoin (45), the hemiketal-pyran linkage required differential substitution (Scheme 9) and demonstrated the power of the sequential double addition strategy.14 Treatment of bis-epoxide S,S-4 with a stoichiometric amount of (benzyloxy)methyllithium 38 and BF3?OEt2 in THF at –78 °C provided monoaddition adduct 39, which was then treated with the organolithium formed from transmetallation of 2,2-bis-(tributyltin)dithiane 40. This single-pot procedure afforded dithiane diol 41 in 56% overall yield. Subsequent acetonide formation and transmetallation provided a competent nucleophile for direct displacement of dibromide 42, which itself was derived from dichlorodiol R,R-3. The resulting bis-acetonide (43) was obtained in 60% overall yield and provided a rapid access to tris-acetonide 44, a key intermediate for the synthesis of the hemiketal-pyran moiety of 45. Similar sequential addition strategies have proven to be useful as well.
roflamycoin synthesis
roflamycoin Preparation Products And Raw materials
Tag:roflamycoin(77814-07-4) Related Product Information
TS 155-2 Hygrolidin TS 155-2