Regioselective reductive ring opening of 4-methoxybenzylidene acetals of hexopyranosides. Access to a novel protective group strategy

Journal of the Chemical Society Chemical Communications ◽

10.1039/c39840000201 ◽

1984 ◽

pp. 201 ◽

Cited By ~ 61

Author(s):

Rolf Johansson ◽

Bertil Samuelsson

Keyword(s):

Ring Opening ◽

Protective Group ◽

Group Strategy

Download Full-text

ChemInform Abstract: REGIOSELECTIVE REDUCTIVE RING OPENING OF 4-METHOXYBENZYLIDENE ACETALS OF HEXOPYRANOSIDES. ACCESS TO A NOVEL PROTECTIVE GROUP STRATEGY

Chemischer Informationsdienst ◽

10.1002/chin.198423304 ◽

1984 ◽

Vol 15 (23) ◽

Author(s):

R. JOHANSSON ◽

B. SAMUELSSON

Keyword(s):

Ring Opening ◽

Protective Group ◽

Group Strategy

Download Full-text

The Utility of a 3-O-Allyl Group as a Protective Group for Ring-Opening Polymerization of α-d-Glucopyranose 1,2,4-Orthopivalate Derivatives

Biomacromolecules ◽

10.1021/bm015656e ◽

2002 ◽

Vol 3 (3) ◽

pp. 538-546 ◽

Cited By ~ 16

Author(s):

Makoto Karakawa ◽

Hiroshi Kamitakahara ◽

Toshiyuki Takano ◽

Fumiaki Nakatsubo

Keyword(s):

Ring Opening ◽

Ring Opening Polymerization ◽

Protective Group

Download Full-text

Synthesis of Polyfunctional Pentaerythritol-Derivatives Using a Novel Protective Group Strategy for the Preparation of Cluster-Glycolipids

Synlett ◽

10.1055/s-2000-6739 ◽

2000 ◽

Vol 2000 (08) ◽

pp. 1157-1159

Keyword(s):

Protective Group ◽

Group Strategy

Download Full-text

Regioselective reductive ring-opening of 4-methoxybenzylidene acetals of hexopyranosides. Access to a novel protecting-group strategy. Part 1

Journal of the Chemical Society Perkin Transactions 1 ◽

10.1039/p19840002371 ◽

1984 ◽

pp. 2371 ◽

Cited By ~ 207

Author(s):

Rolf Johansson ◽

Bertil Samuelsson

Keyword(s):

Ring Opening ◽

Protecting Group ◽

Group Strategy

Download Full-text

ChemInform Abstract: New Synthetic Methods Emphasizing Deoxyfluoro Sugars and Protective Group Strategy

ChemInform ◽

10.1002/chin.199033348 ◽

1990 ◽

Vol 21 (33) ◽

Author(s):

W. A. SZAREK

Keyword(s):

Synthetic Methods ◽

Protective Group ◽

Group Strategy

Download Full-text

Aptamer protective groups tolerate different reagents and reactions for regioselective modification of neomycin B

Organic & Biomolecular Chemistry ◽

10.1039/d0ob02104k ◽

2020 ◽

Vol 18 (47) ◽

pp. 9606-9610

Author(s):

Andreas A. Bastian ◽

Agnieszka Gruszka ◽

Philippe Jung ◽

Andreas Herrmann

Keyword(s):

Protective Group ◽

Reaction Conditions ◽

Group Strategy ◽

Protective Groups ◽

Neomycin B ◽

Regioselective Modification

The aptameric protective group strategy is compatible with diverse reagents and reaction conditions for the synthesis of new neomycin B derivatives.

Download Full-text

ChemInform Abstract: REGIOSELECTIVE REDUCTIVE RING-OPENING OF 4-METHOXYBENZYLIDENE ACETALS OF HEXOPYRANOSIDES. ACCESS TO A NOVEL PROTECTING-GROUP STRATEGY. PART 1

Chemischer Informationsdienst ◽

10.1002/chin.198504315 ◽

1985 ◽

Vol 16 (4) ◽

Author(s):

R. JOHANSSON ◽

B. SAMUELSSON

Keyword(s):

Ring Opening ◽

Protecting Group ◽

Group Strategy

Download Full-text

Practical Total Synthesis of Ciguatoxin CTX3C by Improved Protective Group Strategy

Organic Letters ◽

10.1021/ol027105m ◽

2002 ◽

Vol 4 (25) ◽

pp. 4551-4554 ◽

Cited By ~ 94

Author(s):

Masayuki Inoue ◽

Hisatoshi Uehara ◽

Megumi Maruyama ◽

Masahiro Hirama

Keyword(s):

Total Synthesis ◽

Protective Group ◽

Group Strategy

Download Full-text

New Synthetic Methods Emphasizing Deoxyfluoro Sugars and Protective-Group Strategy

ACS Symposium Series - Trends in Synthetic Carbohydrate Chemistry ◽

10.1021/bk-1989-0386.ch001 ◽

1989 ◽

pp. 2-21 ◽

Cited By ~ 3

Author(s):

Walter A. Szarek

Keyword(s):

Synthetic Methods ◽

Protective Group ◽

Group Strategy

Download Full-text

Amino-functional polyethers: versatile, stimuli-responsive polymers

Polymer Chemistry ◽

10.1039/d0py00466a ◽

2020 ◽

Vol 11 (24) ◽

pp. 3940-3950 ◽

Cited By ~ 2

Author(s):

Patrick Verkoyen ◽

Holger Frey

Keyword(s):

Ring Opening ◽

Review Article ◽

Stimuli Responsive ◽

New Class ◽

Stimuli Responsive Polymers ◽

Responsive Polymers

Amino-functional polyethers have emerged as a new class of “smart”, i.e. pH- and thermoresponsive materials. This review article summarizes the synthesis and applications of these materials, obtained from ring-opening of suitable epoxide monomers.

Download Full-text