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T N
NH
OH
Ru
OH
N
Sm
H 2
Cl
NH 2
O
O
I
( R , R )- 126
(1 R ,2 S )- 128
( S , R , R )- 129
( S , S )- 127
N
X
O
NHCH 3
N
H
H
N
N
Fe
Ph 2 P
N
OH
N
PPh 2 PPh 2
X
H
( S )- 131
( S , S )- 130
( S , S )- 132
X=S:( R , R )- 133
X=O:( R , R ) -134
HO
P
HN
O
PXyl 2
N
ON
N
N
O
O
PXyl 2
( R , R )- 136
( S )- 135
138
( S )- 137
O
O
S
NHTs
O
PCy 2
N
Fe
Cl
N
Ru
Ru
NH 2
O
H
Ph 2
N
H 2
Cl
Cl
H
H
139
( R , S )- 141
( R , R) - 142
( S , S )- 140
S
Ph
Ph
O
T N
T N
OH
H
H
Ru
Rh
NH
NH
H
HN
Boc
Boc
Cl
Cl
( S , S )- 146
( S , S )- 145
( S,S) - 143
( S,S) - 144
O
P
P
P
N
N
O
O
N Os
P
O
O
N
Ph
Ph
N
N
NH 2
Cl
Ph
Ph
Me
( R , R )- 147
P-P = ( S , R )-Josiphos
( S , R )- 148
( R , R )- 149
Figure 7.26. Catalysts for transfer hydrogenation of ketones.
 
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