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Aluminate! 1- , tetrahydro-, lithium

In a more general sense, this reduction method provides a convenient pathway for converting an aromatic carboxyl group to a methyl group (see Table I).7 Previously, this transformation has been achieved by reduction of the acid to the alcohol with lithium aluminum hydride, conversion of the alcohol to the tosylate, and a second reduction either with lithium aluminum hydride [Aluminate(l —), tetrahydro, lithium,... [Pg.86]

This mixture is available from Aldrich Chemical Company, Inc. The checkers used a 7 93 mixture of the cis- and traws isomers, prepared by lithium aluminum hydride [Aluminate(l —), tetrahydro-, lithium, (T-4)-] reduction of 4-ferf-butylcyclohexanone and recrystallization of the crude product. The ketone was purchased from Aldrich Chemical Company, Inc. [Pg.100]

Phenanthrenequinone (8) 9,10-Phenanthrenedione (9) (84-11-7) Lithium aluminum hydride Aluminate (1-), tetrahydro, lithium (8), Aluminate (1-), tetrahydro-, lithium, (T-4)- (9) (16853-85-3) N,/V-Dimethylformamide dimethyl acetal Trimethylamine, 1,1-dimethoxy- (8) Methanamine, 1,1-dimethoxy-(V,N-dimethyl- (9) (4637-24-5)... [Pg.16]

Lithium aluminum hydride Aluminate(l-), tetrahydro-, lithium... [Pg.36]

Lithium aluminum hydride Aluminate (1-), tetrahydro-, lithium (8) Aluminate (1-), tetrahydro-, lithium (I-4)- (9) (16853-85-3)... [Pg.77]


See other pages where Aluminate! 1- , tetrahydro-, lithium is mentioned: [Pg.11]    [Pg.131]    [Pg.142]    [Pg.169]    [Pg.36]    [Pg.195]    [Pg.42]    [Pg.258]    [Pg.130]    [Pg.239]    [Pg.37]    [Pg.163]    [Pg.22]    [Pg.148]    [Pg.19]   
See also in sourсe #XX -- [ Pg.3 , Pg.4 , Pg.54 , Pg.56 , Pg.56 , Pg.57 , Pg.102 ]

See also in sourсe #XX -- [ Pg.3 , Pg.4 , Pg.54 , Pg.56 , Pg.56 , Pg.57 , Pg.102 ]

See also in sourсe #XX -- [ Pg.3 , Pg.4 , Pg.102 ]

See also in sourсe #XX -- [ Pg.3 , Pg.42 , Pg.61 ]




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ALUMINIC

Alumin

Alumination

Aluminization

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