AAAAAA

   
Results: 1-12 |
Results: 12
Approaches to the synthesis of (+)- and (-)-epibatidine
Authors: Barros, MT Maycock, CD Ventura, MR
Citation: Mt. Barros et al., Approaches to the synthesis of (+)- and (-)-epibatidine, J CHEM S P1, (2), 2001, pp. 166-173
The effect of diethylamine on Stille alkylations with tetraalkylstannanes
Authors: Barros, MT Maycock, CD Madureira, MI Ventura, MR
Citation: Mt. Barros et al., The effect of diethylamine on Stille alkylations with tetraalkylstannanes, CHEM COMMUN, (17), 2001, pp. 1662-1663
Bromine in methanol: An efficient reagent for the deprotection of the tert-butyldiphenylsilyl group
Authors: Barros, MT Maycock, CD Thomassigny, C
Citation: Mt. Barros et al., Bromine in methanol: An efficient reagent for the deprotection of the tert-butyldiphenylsilyl group, SYNLETT, (7), 2001, pp. 1146-1148
The first synthesis of (-)-asperpentyn and efficient syntheses of (+)-harveynone, (+)-epiepoformin and (-)-theobroxide
Authors: Barros, MT Maycock, CD Ventura, MR
Citation: Mt. Barros et al., The first synthesis of (-)-asperpentyn and efficient syntheses of (+)-harveynone, (+)-epiepoformin and (-)-theobroxide, CHEM-EUR J, 6(21), 2000, pp. 3991-3996
Metabolism of 3-C-13-malate in primary cultures of mouse astrocytes
Authors: Alves, PM Nunes, R Zhang, CH Maycock, CD Sonnewald, U Carrondo, MJT Santos, H
Citation: Pm. Alves et al., Metabolism of 3-C-13-malate in primary cultures of mouse astrocytes, DEV NEUROSC, 22(5-6), 2000, pp. 456-462
Fast galloylation of a sugar moiety: Preparation of three monogalloylsucroses as references for antioxidant activity. A method for the selective deprotection of tert-butyldiphenylsilyl ethers
Authors: Barros, MT Maycock, CD Sineriz, F Thomassigny, C
Citation: Mt. Barros et al., Fast galloylation of a sugar moiety: Preparation of three monogalloylsucroses as references for antioxidant activity. A method for the selective deprotection of tert-butyldiphenylsilyl ethers, TETRAHEDRON, 56(35), 2000, pp. 6511-6516
Preparation of sucrose heptaesters unsubstituted at the C-1 hydroxy group of the fructose moiety via selective O-desilylation
Authors: Barros, MT Maycock, CD Thomassigny, C
Citation: Mt. Barros et al., Preparation of sucrose heptaesters unsubstituted at the C-1 hydroxy group of the fructose moiety via selective O-desilylation, CARBOHY RES, 328(3), 2000, pp. 419-423
The alkylation of a novel acetal derived from (2R,3R)-(+)-tartaric acid: An unexpected rearrangement
Authors: Barros, MT Burke, AJ Maycock, CD
Citation: Mt. Barros et al., The alkylation of a novel acetal derived from (2R,3R)-(+)-tartaric acid: An unexpected rearrangement, TETRAHEDR L, 40(8), 1999, pp. 1583-1586
The effect of DMSO on the borohydride reduction of a cyclohexanone: A formal enantioselective synthesis of (+)-epibatidine.
Authors: Barros, MT Maycock, CD Ventura, MR
Citation: Mt. Barros et al., The effect of DMSO on the borohydride reduction of a cyclohexanone: A formal enantioselective synthesis of (+)-epibatidine., TETRAHEDR L, 40(3), 1999, pp. 557-560
Stereoselective azide introduction during 1,2-sulfur migration in alpha-hydroxyalkyldithioacetals
Authors: Afonso, CAM Barros, MT Maycock, CD
Citation: Cam. Afonso et al., Stereoselective azide introduction during 1,2-sulfur migration in alpha-hydroxyalkyldithioacetals, TETRAHEDRON, 55(3), 1999, pp. 801-814
An efficient transformation of quinic acid to shikimic acid derivatives
Authors: Alves, C Barros, MT Maycock, CD Ventura, MR
Citation: C. Alves et al., An efficient transformation of quinic acid to shikimic acid derivatives, TETRAHEDRON, 55(28), 1999, pp. 8443-8456
The enantioselective total synthesis of epoformin and analogues
Authors: Barros, MT Maycock, CD Ventura, MR
Citation: Mt. Barros et al., The enantioselective total synthesis of epoformin and analogues, TETRAHEDRON, 55(11), 1999, pp. 3233-3244
Risultati: 1-12 |