can you show how synthesis would work HO on t Heo r = s = H from > x e Gerice units J. Brac Hz H₂ Har (listlar I Lindlon
what are the reagents for this retro synthesis? Ho = = =
Question 6 How would you accomplish the following synthesis? HC HO CH. A 1. NBS, light 2. NaOH 3. Ti[OCH(CH3)214 (-)-DET to-oh 1. H2, Pt 2. HBr, ROOR 3. MCPBA -OOH D None of the above с МСРВА
formulate a 4 step synthesis. reagents listed OH 4-STEP SYNTHESIS HO 2 NaNH, NaH
complete all the synthesis problems. OH Br OH OH HO OH OH Br OH OH HO OH
demostrate the necesary reactives in the right order for the synthesis OH OH HO
Provide the synthesis pathway including all reagents and intermediate products. HO.
Would this proposed synthesis work? - What if I replaced pyridine with AlCl3? 2 nor کم my letter و۸ و پنیر ng or
OCH3 OH from One route to the synthesis of HO and CH,CH2MgBr is to 1) protect the ketone as an acetal, 2) reduce the ester to an alcohol, 3) hydrolyze the acetal back to the ketone, 4) protect the alcohol as a TMS ether, 5) react the ketone with the Grignard reagent followed by acidic workup to give the desired product. A second route to the desired product would start with the selective reduction of only the ketone to an...
Part A Choose the reagents that would be required to carry out the following synthesis: CH 2 OH он H20, H+ O 1 . BH3; 2. HO, H202, H2O 03 followed by (CH3) 2S KMnO4, HO (warm, concd.) KMnO4, HO (cold, dilute) Submit Request Answer