All articles by Jyoti Chattopadhyaya
11 articlesArticles in volume 36b (1982)
| 5'-O-Trityl Group Promoted Directive Effect in the Preparation of 2'-O-Methylribonucleosides. Heikkilä, Jarmo; Björkman, Sven; Öberg, Bo; Chattopadhyaya, Jyoti Pages: 715-717. DOI number: 10.3891/acta.chem.scand.36b-0715 |
Articles in volume 37b (1983)
| 3-N-Acyl Uridines: Preparation and Properties of a New Class of Uracil Protecting Group. Welch, Christopher J.; Chattopadhyaya, Jyoti Pages: 147-150. DOI number: 10.3891/acta.chem.scand.37b-0147 |
| The 9-Fluorenylmethoxycarbonyl (Fmoc) Group for the Protection of Amino Functions of Cytidine, Adenosine, Guanosine and Their 2'-Deoxysugar Derivatives. Heikkilä, Jarmo; Chattopadhyaya, Jyoti Pages: 263-265. DOI number: 10.3891/acta.chem.scand.37b-0263 |
| The 2-Nitrophenylsulfenyl (Nps) Group for the Protection of Amino Functions of Cytidine, Adenosine, Guanosine and Their 2'-Deoxysugar Derivatives. Heikkilä, Jarmo; Balgobin, Neil; Chattopadhyaya, Jyoti Pages: 857-862. DOI number: 10.3891/acta.chem.scand.37b-0857 |
Articles in volume 38b (1984)
| Synthesis of D-Psico- and D-Fructofuranosyl Nucleosides. Grouiller, Annie; Chattopadhyaya, Jyoti Pages: 367-373. DOI number: 10.3891/acta.chem.scand.38b-0367 |
Articles in volume 39b (1985)
| An Efficient Conversion of a Ribonucleoside to the Corresponding 2'-Keto-3'-deoxyribonucleoside by a Grignard Reagent. Juntunen, Seppo; Chattopadhyaya, Jyoti Pages: 149-152. DOI number: 10.3891/acta.chem.scand.39b-0149 |
| Some Aspects of the Reaction of Arenesulfenyl chlorides with Hydroxyl Functions of Ribonucleosides. Bazin, Hervé; Heikkilä, Jarmo; Chattopadhyaya, Jyoti Pages: 391-400. DOI number: 10.3891/acta.chem.scand.39b-0391 |
| A Convenient Preparation of N-Protected Nucleosides with the 2,2,2-Trichloro-t-butyloxycarbonyl (TCBOC) Group. Structural Assignment of N,N-bis-TCBOC Guanoside and Its 2'-Deoxy Analogue. Zhou, Xiao-Xiong; Ugi, Ivar; Chattopadhyaya, Jyoti Pages: 761-765. DOI number: 10.3891/acta.chem.scand.39b-0761 |
| Use of 2-Phenylsulfonylethyl as a Phosphate Protecting Group in DNA Synthesis Using the Phosphite-Triester Approach. Balgobin, Neil; Chattopadhyaya, Jyoti Pages: 883-888. DOI number: 10.3891/acta.chem.scand.39b-0883 |
Articles in volume 41b (1987)
| Phosphitylation of Guanine or Inosine Bases during the Preparation of Nucleoside Phosphoramidites. Isolation of Model Products as Thiophosphoric Amide Derivatives and Structure Elucidation by 15N NMR Spectroscopy. Nielsen, John; Dahl, Otto; Remaud, Gerald; Chattopadhyaya, Jyoti Pages: 633-639. DOI number: 10.3891/acta.chem.scand.41b-0633 |
Articles in volume 43 (1989)
| Synthesis and Conformation of 9-(3'-C-Methyl-beta-D-xylo-furanosyl)adenine and 3'-C-Methyladenosine, Two Sugar-Methylated Nucleoside Analogues. Koole, Leo H.; Buck, Henk M.; Vial, Jean-Marc; Chattopadhyaya, Jyoti Pages: 665-669. DOI number: 10.3891/acta.chem.scand.43-0665 |



