Front | Back |
Carb with ac2o and pyridine
|
Ac added to every o except the one inside the ring.
|
Carb with ch3i, ag2o, and h3o+
|
Methyl added to every o except the one inside the ring. (ether formation)
|
Carb with meOH and hcl
|
Methyl added to right corner o (glycosylation)
|
Carb with cu2+
|
Replace top hco with co2h
|
Carb with h- and nabh4
|
Removes =o and replaces with oh. when not done at top =o, wavy line to oh)
|
Carb with h2o and hno3
|
Top cho > co2h. bot oh > co2h. (optically active if there is no vertical symmetry)
|
Carb with nacn, pd/h2, then h3o+
|
Additional c-oh 2nd to top (kiliawi-fischer chain extension)
|
Carb with h2noh, ac20/aco-, then naome
|
Removes second to top c-oh (wohl degredation)
|
Add ac to every o except the one inside the ring.
|
Ac2o and pyridine
|
Ac added to every o except the one inside the ring.
|
Ac2o and pyridine
|
Methyl added to every o except the one inside the ring. (ether formation)
|
Ch3i, ag2o, and h3o+
|
Methyl added to right corner o (glycosylation)
|
Meoh and hcl
|
Replace top hco with co2h
|
Cu2+
|
Removes =o and replaces with oh. when not done at top =o, wavy line to oh)
|
Nabh4, h-
|
Top cho > co2h. bot oh > co2h. (optically active if there is no vertical symmetry)
|
H2o, hno3
|