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1.
Org Lett ; 3(25): 4007-10, 2001 Dec 13.
Article in English | MEDLINE | ID: mdl-11735571

ABSTRACT

[reaction: see text] A surprising and synthetically useful counterion-dependent reversal of diastereoselectivity was found in 1,2-additions of hard carbon nucleophiles to C(6)-heterosubstituted cyclohexenones. In general, Grignard reagents added syn to the C(6)-substituent and Li reagents added anti, although some exceptions were found. Selectivities could be increased in some cases by appropriate choice of solvent and/or cosolvent.


Subject(s)
Hydrocarbons, Cyclic/chemistry , Antineoplastic Agents, Phytogenic/chemistry , Carbazoles , Cyclohexanones/chemistry , Diterpenes , Indoles/chemistry , Lithium/chemistry , Magnesium Compounds/chemistry , Molecular Conformation , Molecular Structure , Pyrroles/chemistry , Spiro Compounds/chemistry , Stereoisomerism
7.
Science ; 152(3726): 1282-3, 1966 May 27.
Article in English | MEDLINE | ID: mdl-5937124
8.
Science ; 151(3710): 576-7, 1966 Feb 04.
Article in English | MEDLINE | ID: mdl-5903582

ABSTRACT

The survival rate of groups of female mice given a standard dose of pentobarbital sodium varied during a 12-hour period. When survival rate was plotted against time, a curve with several inflections was described.


Subject(s)
Pentobarbital/toxicity , Animals , Injections, Intraperitoneal , Mice , Mortality , Periodicity , Time
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