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
Achiral as well as chiral 2,3-olefinic acetals are converted into 2- and 3- hydroxy acetals via LAH ...
Sodium borohydride (0.4–1.5 equivalents) in the presence of ammonium oxalate (0.2 equivalents) reduc...
The stereochemical course of the reaction catalysed by C-C hydrolase BphD from Burkholderia xenovora...
It was shown that the hydrogenolysis of 4-acetyl-3α,4α-epoxycarane using NaBH4 is accomplished stere...
In this paper we describe the reduction by NaBH4 of some cyclopentanones containing an oxygenated fu...
ABSTRACT. Diastereoselective reduction of 2,3-dioxo-4-carboxy-5-(substituted)pyrrolidine 1 by NaBH4/...
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...
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...
1-benzyl-3,3-dimethyl-5-methylenepyrrolidine-2,4-dione is an intermediate product produced in the sy...
Two stereochemical functions of the cholesteryl group were investigated and are described in Section...
The (dl) α‐keto esters 16, were prepared from the (dl) carbinols 1 to 4 and from (dl)‐2‐hydroxyhepta...
YesThe stereochemical outcome of the epoxidation of Δ14–15 cholestanes with mCPBA is controlled by t...
1. In presence of Raney nickel, 2,3-epoxypinane is reduced with formation of two alcohols of composi...
Achiral as well as chiral 2,3-olefinic acetals are converted into 2- and 3- hydroxy acetals via LAH ...
Sodium borohydride (0.4–1.5 equivalents) in the presence of ammonium oxalate (0.2 equivalents) reduc...
The stereochemical course of the reaction catalysed by C-C hydrolase BphD from Burkholderia xenovora...
It was shown that the hydrogenolysis of 4-acetyl-3α,4α-epoxycarane using NaBH4 is accomplished stere...
In this paper we describe the reduction by NaBH4 of some cyclopentanones containing an oxygenated fu...
ABSTRACT. Diastereoselective reduction of 2,3-dioxo-4-carboxy-5-(substituted)pyrrolidine 1 by NaBH4/...
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...
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...
1-benzyl-3,3-dimethyl-5-methylenepyrrolidine-2,4-dione is an intermediate product produced in the sy...
Two stereochemical functions of the cholesteryl group were investigated and are described in Section...
The (dl) α‐keto esters 16, were prepared from the (dl) carbinols 1 to 4 and from (dl)‐2‐hydroxyhepta...
YesThe stereochemical outcome of the epoxidation of Δ14–15 cholestanes with mCPBA is controlled by t...
1. In presence of Raney nickel, 2,3-epoxypinane is reduced with formation of two alcohols of composi...
Achiral as well as chiral 2,3-olefinic acetals are converted into 2- and 3- hydroxy acetals via LAH ...
Sodium borohydride (0.4–1.5 equivalents) in the presence of ammonium oxalate (0.2 equivalents) reduc...
The stereochemical course of the reaction catalysed by C-C hydrolase BphD from Burkholderia xenovora...