- 2-Mercaptoethanol (also β-mercaptoethanol, BME, 2BME, 2-ME or β-met) is the
chemical compound with the
formula HOCH2CH2SH. ME or βME, as it is commonly...
-
alcohol ROH and
lithium carbonate, the OR
replaces the
bromine and on
deprotecting the
acetylated hydroxyls the
product is
synthesized in
relatively high...
- It is also used as a
phase transfer catalyst and as a mild base. As a
deprotecting agent, TBAF in DMSO will
convert O-silylated
enolates into carbonyls...
- pKa of the
thiol groups is 9.2 and 10.1. DTT is used as a
reducing or "
deprotecting"
agent for
thiolated DNA. The
terminal sulfur atoms of
thiolated DNA...
- in
organic synthesis mainly as a
deoxygenating agent. It is used for
deprotecting acetals and
ketals to
aldehydes and ketones, and for
converting epoxides...
- The TES
protecting group on the
carbon 8
hydroxyl was
removed without deprotecting any of the
other groups, and then the
carbon 8
hydroxyl was oxidized...
-
tetrafluoroborate and
boron trifluoride etherate were also
developed to
deprotect SEM group. Lipshutz,
Bruce H.; Pegram,
Joseph J. (1980). "β-(Trimethylsilyl)ethoxymethyl...
- mercury(II) for
sulfur ligands, Hg(OAc)2 can be used as a
reagent to
deprotect thiol groups in
organic synthesis.
Similarly Hg(OAc)2 has been used to...
-
acetonitrile followed by
methanol is a mild and
versatile method of
deprotecting Boc-protected amines. The use of
triethylsilane as a
carbocation scavenger...
-
soluble source of
pyridinium (C5H5NH+) ions. For example, PPTS is used to
deprotect silyl ethers or
tetrahydropyranyl ethers when a
substrate is unstable...
