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1
Key Chiral Auxiliary Applications
Greg Roos (Auth.)
product
config
tetrahedron
lda
buli
substrate
reagent
refs
org
co2me
auxiliary
overall
chiral
ticl4
key
ho2c
soc
dipea
asymmetry
bu2botf
addition
obn
derivatives
meo2c
bnbr
related
co2et
co2h
endo:exo
nahmds
reactions
nh2
licl
lhmds
oac
alkylation
pmp
hmpa
enders
phcho
no2
ohc
tms
h2n
prcho
bonds
zncl2
bno
khmds
commun
Godina:
2014
Jezik:
english
Fajl:
PDF, 74.35 MB
Vaši tagovi:
0
/
0
english, 2014
2
The Claisen Rearrangement: Methods and Applications
Wiley-VCH
Martin Hiersemann
,
Udo Nubbemeyer
rearrangement
claisen
allyl
reaction
transition
synthesis
ºc
allylic
soc
vinyl
ketene
enolate
tetrahedron
thf
ether
org
product
ester
esters
rearrangements
lda
bond
obtained
acetal
anti
formation
silyl
chiral
reported
oet
products
reflux
diastereoselectivity
aliphatic
observed
corresponding
mol
co2me
asymmetric
amino
obn
rate
substrate
substituent
substituted
catalyzed
johnson
aromatic
otbs
alcohol
Godina:
2007
Jezik:
english
Fajl:
PDF, 9.90 MB
Vaši tagovi:
0
/
0
english, 2007
3
Two Hundred Exercises In Mechanistic Organic Chemistry
GalChimia
G. Suarez
attacks
alcohol
producing
oxygen
formation
intramolecularly
hemiacetal
ketone
lactone
aldehyde
resulting
carbonyl
acidic
j.org.chem
acetal
epoxide
reacts
nitrogen
produces
alkoxide
tetrahedron
amine
cation
carbocation
org.chem
hydroxy
thf
anion
hydrolysis
membered
opening
meoh
obn
protonation
groups
bno
displaces
elimination
ester
expulsion
alkene
protonated
reaction
atom
alcohols
imine
reactions
formed
mechanism
methanol
Godina:
2002
Jezik:
english
Fajl:
PDF, 3.52 MB
Vaši tagovi:
0
/
0
english, 2002
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