Add to ORKGIt was shown that the hydrogenolysis of 4-acetyl-3α,4α-epoxycarane using NaBH4 is accomplished stereoselectively in harmony with its steric structure. © 1979 Plenum Publishing Corporation
Two stereochemical functions of the cholesteryl group were investigated and are described in Section...
Includes bibliographical references (pages [44]-49)A study of the ester to ether reduction by sodium...
The reduction of racemic 8-hydroxy-6-methoxy-3,3-dimethyl-3,4,5,6,6a,12a-hexahydrobenz[a]anthracene...
It was shown that the hydrogenolysis of 4-acetyl-3α,4α-epoxycarane using NaBH4 is accomplished stere...
The acid hydrolysis of 4-acetyl-3α,4α-epoxycarane proceeds with opening of the oxide ring at the car...
An unusual reduction of some aromatic aldehydes and ketones by sodium borohydride was discovered. In...
3 β-Acetyl-α-3,4-epoxycarane under the influence of bases is easily rearranged to the α, β-unsaturat...
In this paper we describe the reduction by NaBH4 of some cyclopentanones containing an oxygenated fu...
1-benzyl-3,3-dimethyl-5-methylenepyrrolidine-2,4-dione is an intermediate product produced in the sy...
1. In presence of Raney nickel, 2,3-epoxypinane is reduced with formation of two alcohols of composi...
ABSTRACT. Diastereoselective reduction of 2,3-dioxo-4-carboxy-5-(substituted)pyrrolidine 1 by NaBH4/...
A new synthetic route to anti-alpha,beta-dihydroxy esters has been developed. The new method consist...
Reduction of trans-1-oxo-7-methoxy-1,2,3,4,9,10,11,12-octahydrophenanthrene (XI) by lithium tri-t-bu...
Epoxldation of diastereomeric 4-(hydroxyethyl)- and 4-(acetoxyethyl)-3-carenes stereospecifically gi...
Sodium borohydride (0.4–1.5 equivalents) in the presence of ammonium oxalate (0.2 equivalents) reduc...
Two stereochemical functions of the cholesteryl group were investigated and are described in Section...
Includes bibliographical references (pages [44]-49)A study of the ester to ether reduction by sodium...
The reduction of racemic 8-hydroxy-6-methoxy-3,3-dimethyl-3,4,5,6,6a,12a-hexahydrobenz[a]anthracene...
It was shown that the hydrogenolysis of 4-acetyl-3α,4α-epoxycarane using NaBH4 is accomplished stere...
The acid hydrolysis of 4-acetyl-3α,4α-epoxycarane proceeds with opening of the oxide ring at the car...
An unusual reduction of some aromatic aldehydes and ketones by sodium borohydride was discovered. In...
3 β-Acetyl-α-3,4-epoxycarane under the influence of bases is easily rearranged to the α, β-unsaturat...
In this paper we describe the reduction by NaBH4 of some cyclopentanones containing an oxygenated fu...
1-benzyl-3,3-dimethyl-5-methylenepyrrolidine-2,4-dione is an intermediate product produced in the sy...
1. In presence of Raney nickel, 2,3-epoxypinane is reduced with formation of two alcohols of composi...
ABSTRACT. Diastereoselective reduction of 2,3-dioxo-4-carboxy-5-(substituted)pyrrolidine 1 by NaBH4/...
A new synthetic route to anti-alpha,beta-dihydroxy esters has been developed. The new method consist...
Reduction of trans-1-oxo-7-methoxy-1,2,3,4,9,10,11,12-octahydrophenanthrene (XI) by lithium tri-t-bu...
Epoxldation of diastereomeric 4-(hydroxyethyl)- and 4-(acetoxyethyl)-3-carenes stereospecifically gi...
Sodium borohydride (0.4–1.5 equivalents) in the presence of ammonium oxalate (0.2 equivalents) reduc...
Two stereochemical functions of the cholesteryl group were investigated and are described in Section...
Includes bibliographical references (pages [44]-49)A study of the ester to ether reduction by sodium...
The reduction of racemic 8-hydroxy-6-methoxy-3,3-dimethyl-3,4,5,6,6a,12a-hexahydrobenz[a]anthracene...