skip to main content
Idioma:
Resultados 1 2 3 next page
Refinado por: Nome da Publicação: Journal Of Organic Chemistry remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
An efficient asymmetric synthesis of tarchonanthuslactone
An efficient asymmetric synthesis of tarchonanthuslactone
Material Type:
Artigo 		Adicionar ao Meu Espaço

An efficient asymmetric synthesis of tarchonanthuslactone

Reddy, M V ; Yucel, A J ; Ramachandran, P V

Journal of organic chemistry, 2001-04, Vol.66 (7), p.2512-2514 [Periódico revisado por pares]

United States

Texto completo disponível

Citações Citado por
2
A facile synthesis of perfluoroalkyl vinyl iodides and their palladium-mediated cross-coupling reactions
A facile synthesis of perfluoroalkyl vinyl iodides and their palladium-mediated cross-coupling reactions
Material Type:
Artigo 		Adicionar ao Meu Espaço

A facile synthesis of perfluoroalkyl vinyl iodides and their palladium-mediated cross-coupling reactions

Jennings, M P ; Cork, E A ; Ramachandran, P V

Journal of organic chemistry, 2000-12, Vol.65 (25), p.8763-8766 [Periódico revisado por pares]

United States

Texto completo disponível

Citações Citado por
3
Chiral synthesis via organoboranes. 18. Selective reductions. 43. Diisopinocampheylchloroborane as an excellent chiral reducing reagent for the synthesis of halo alcohols of high enantiomeric purity. A highly enantioselective synthesis of both optical isomers of Tomoxetine, Fluoxetine, and Nisoxetine
Chiral synthesis via organoboranes. 18. Selective reductions. 43. Diisopinocampheylchloroborane as an excellent chiral reducing reagent for the synthesis of halo alcohols of high enantiomeric purity. A highly enantioselective synthesis of both optical isomers of Tomoxetine, Fluoxetine, and Nisoxetine
Material Type:
Artigo 		Adicionar ao Meu Espaço

Chiral synthesis via organoboranes. 18. Selective reductions. 43. Diisopinocampheylchloroborane as an excellent chiral reducing reagent for the synthesis of halo alcohols of high enantiomeric purity. A highly enantioselective synthesis of both optical isomers of Tomoxetine, Fluoxetine, and Nisoxetine

Srebnik, Morris ; Ramachandran, P. V ; Brown, Herbert C

Journal of organic chemistry, 1988-06, Vol.53 (13), p.2916-2920 [Periódico revisado por pares]

American Chemical Society

Texto completo disponível

Citações Citado por
4
Diisopinocampheylchloroborane, a remarkably efficient chiral reducing agent for aromatic prochiral ketones
Diisopinocampheylchloroborane, a remarkably efficient chiral reducing agent for aromatic prochiral ketones
Material Type:
Artigo 		Adicionar ao Meu Espaço

Diisopinocampheylchloroborane, a remarkably efficient chiral reducing agent for aromatic prochiral ketones

Chandrasekharan, J ; Ramachandran, P. V ; Brown, Herbert C

Journal of organic chemistry, 1985-12, Vol.50 (25), p.5446-5448 [Periódico revisado por pares]

Washington, DC: American Chemical Society

Texto completo disponível

Citações Citado por
5
Chiral synthesis via organoboranes. 22. Selective reductions. 44. The effect of the steric requirements of the alkyl substituent in isopinocampheylalkylchloroboranes for the asymmetric reduction of representative ketones
Chiral synthesis via organoboranes. 22. Selective reductions. 44. The effect of the steric requirements of the alkyl substituent in isopinocampheylalkylchloroboranes for the asymmetric reduction of representative ketones
Material Type:
Artigo 		Adicionar ao Meu Espaço

Chiral synthesis via organoboranes. 22. Selective reductions. 44. The effect of the steric requirements of the alkyl substituent in isopinocampheylalkylchloroboranes for the asymmetric reduction of representative ketones

Brown, Herbert C ; Srebnik, Morris ; Ramachandran, P. V

Journal of organic chemistry, 1989-03, Vol.54 (7), p.1577-1583 [Periódico revisado por pares]

American Chemical Society

Texto completo disponível

Citações Citado por
6
Chiral Synthesis of Functionalized Tetrahydropyridines:  γ-Aminobutyric Acid Uptake Inhibitor Analogues
Chiral Synthesis of Functionalized Tetrahydropyridines:  γ-Aminobutyric Acid Uptake Inhibitor Analogues
Material Type:
Artigo 		Adicionar ao Meu Espaço

Chiral Synthesis of Functionalized Tetrahydropyridines:  γ-Aminobutyric Acid Uptake Inhibitor Analogues

Ramachandran, P. Veeraraghavan ; Burghardt, Thomas E ; Bland-Berry, Layla

Journal of organic chemistry, 2005-09, Vol.70 (20), p.7911-7918 [Periódico revisado por pares]

Washington, DC: American Chemical Society

Texto completo disponível

Citações Citado por
7
Highly efficient asymmetric reduction of .alpha.-tertiary alkyl ketones with diisopinocampheylchloroborane
Highly efficient asymmetric reduction of .alpha.-tertiary alkyl ketones with diisopinocampheylchloroborane
Material Type:
Artigo 		Adicionar ao Meu Espaço

Highly efficient asymmetric reduction of .alpha.-tertiary alkyl ketones with diisopinocampheylchloroborane

Brown, Herbert C ; Chandrasekharan, J ; Ramachandran, P. V

Journal of organic chemistry, 1986-08, Vol.51 (17), p.3394-3396 [Periódico revisado por pares]

Washington, DC: American Chemical Society

Texto completo disponível

Citações Citado por
8
Stereoselective Syntheses of (+)-Goniodiol, (−)-8-Epigoniodiol, and (+)-9-Deoxygoniopypyrone via Alkoxyallylboration and Ring-Closing Metathesis
Stereoselective Syntheses of (+)-Goniodiol, (−)-8-Epigoniodiol, and (+)-9-Deoxygoniopypyrone via Alkoxyallylboration and Ring-Closing Metathesis
Material Type:
Artigo 		Adicionar ao Meu Espaço

Stereoselective Syntheses of (+)-Goniodiol, (−)-8-Epigoniodiol, and (+)-9-Deoxygoniopypyrone via Alkoxyallylboration and Ring-Closing Metathesis

Ramachandran, P. Veeraraghavan ; Chandra, J. Subash ; Ram Reddy, M. Venkat

Journal of organic chemistry, 2002-10, Vol.67 (21), p.7547-7550 [Periódico revisado por pares]

Washington, DC: American Chemical Society

Texto completo disponível

Citações Citado por
9
Selective Reductions. 59. Effective Intramolecular Asymmetric Reductions of α-, β-, and γ-Keto Acids with Diisopinocampheylborane and Intermolecular Asymmetric Reductions of the Corresponding Esters with B-Chlorodiisopinocampheylborane
Selective Reductions. 59. Effective Intramolecular Asymmetric Reductions of α-, β-, and γ-Keto Acids with Diisopinocampheylborane and Intermolecular Asymmetric Reductions of the Corresponding Esters with B-Chlorodiisopinocampheylborane
Material Type:
Artigo 		Adicionar ao Meu Espaço

Selective Reductions. 59. Effective Intramolecular Asymmetric Reductions of α-, β-, and γ-Keto Acids with Diisopinocampheylborane and Intermolecular Asymmetric Reductions of the Corresponding Esters with B-Chlorodiisopinocampheylborane

Ramachandran, P. Veeraraghavan ; Pitre, Sangeeta ; Brown, Herbert C

Journal of organic chemistry, 2002-07, Vol.67 (15), p.5315-5319 [Periódico revisado por pares]

Washington, DC: American Chemical Society

Texto completo disponível

Citações Citado por
10
Ozonolysis of trans-di-tert-butylethylene. The oligomer
Ozonolysis of trans-di-tert-butylethylene. The oligomer
Material Type:
Artigo 		Adicionar ao Meu Espaço

Ozonolysis of trans-di-tert-butylethylene. The oligomer

Murray, Robert W ; Ramachandran, V

Journal of organic chemistry, 1983-03, Vol.48 (6), p.813-816 [Periódico revisado por pares]

American Chemical Society

Texto completo disponível

Citações Citado por
Resultados 1 2 3 next page

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.