Chemo-and diastereoselective reduction of. beta.-enamino esters: A convenient synthesis of both cis-and trans-. gamma.-amino alcohols and. beta.-amino esters

G Bartoli, C Cimarelli, E Marcantoni…

Index: Journal of Organic Chemistry, , vol. 59, # 18 p. 5328 - 5335

Full Text: HTML

Citation Number: 210

Abstract

... The development of novel synthetic methods leading to y-amino alcohols and p-amino esters or their deriva- tives constitutes an active area of investigation in synthetic organic chemistry. ... (4) (a) Spatola, AF In Chemistry and Biochemistry ... Reduction of P-Enamino Esters J. Org. ...

Related Articles:

Stereoselective anhydride openings

[Goodridge, Richard J.; Hambley, Trevor W.; Ridley, Damon D. Australian Journal of Chemistry, 1986 , vol. 39, # 4 p. 591 - 604]

A CONVENIENT SYNTHESIS OF cis-(1R)-N-BENZYL-(2S)-(HYDROXYMETHYL) CYCLOHEXYLAMINE

[Organic Preparations and Procedures International, , vol. 24, # 6 p. 685 - 687]

A CONVENIENT SYNTHESIS OF cis-(1R)-N-BENZYL-(2S)-(HYDROXYMETHYL) CYCLOHEXYLAMINE

[Organic Preparations and Procedures International, , vol. 24, # 6 p. 685 - 687]

Preparations and Crystal-Structures of the 2-Oxides of Some Octahydro-3, 2, 1-Benzoxathiazines and Octahydro-2h-3, 1, 2-Benzoxazaphosphorines

[Australian Journal of Chemistry, , vol. 39, # 4 p. 591 - 604]

Preparations and Crystal-Structures of the 2-Oxides of Some Octahydro-3, 2, 1-Benzoxathiazines and Octahydro-2h-3, 1, 2-Benzoxazaphosphorines

[Australian Journal of Chemistry, , vol. 39, # 4 p. 591 - 604]

More Articles...