Synthesis of 3,7-Anhydro-d-glycero-d-ido-octitol 1,5,6-Trisphosphate as an IP3Receptor Ligand Using a Radical Cyclization Reaction with a Vinylsilyl Tether as the Key Step. Conformational Restriction Strategy Using Steric Repulsion between Adjacent Bulky Protecting Groups on a Pyranose Ring

The First Synthesis of Herbicidin B. Stereoselective Construction of the Tricyclic Undecose Moiety by a Conformational Restriction Strategy Using Steric Repulsion between Adjacent Bulky Silyl Protecting Groups on a Pyranose Ring†

Journal of the American Chemical Society ◽

10.1021/ja992608h ◽

1999 ◽

Vol 121 (44) ◽

pp. 10270-10280 ◽

Cited By ~ 58

Author(s):

Satoshi Ichikawa ◽

Satoshi Shuto ◽

Akira Matsuda

Keyword(s):

Protecting Groups ◽

Steric Repulsion ◽

Pyranose Ring ◽

ChemInform Abstract: Synthesis of 3,7-Anhydro-D-glycero-D-ido-octitol 1,5,6-Trisphosphate as an IP3 Receptor Ligand Using a Radical Cyclization Reaction with a Vinylsilyl Tether as the Key Step. Conformational Restriction Strategy Using Steric Repulsion B

ChemInform ◽

10.1002/chin.200051191 ◽

2000 ◽

Vol 31 (51) ◽

pp. no-no

Author(s):

Satoshi Shuto ◽

Yumi Yahiro ◽

Satoshi Ichikawa ◽

Akira Matsuda

Keyword(s):

Radical Cyclization ◽

Cyclization Reaction ◽

Steric Repulsion ◽

Ip3 Receptor ◽

Receptor Ligand ◽

Synthesis of 4,8-anhydro-d-glycero-d-ido-nonanitol 1,6,7-trisphosphate as a novel IP3 receptor ligand using a stereoselective radical cyclization reaction based on a conformational restriction strategy

Tetrahedron ◽

10.1016/j.tet.2005.02.025 ◽

2005 ◽

Vol 61 (15) ◽

pp. 3697-3707 ◽

Cited By ~ 12

Author(s):

Masaru Terauchi ◽

Yumi Yahiro ◽

Hiroshi Abe ◽

Satoshi Ichikawa ◽

Stephen C. Tovey ◽

...

Keyword(s):

Radical Cyclization ◽

Cyclization Reaction ◽

Ip3 Receptor ◽

Receptor Ligand ◽

Synthesis of C-glycosides via radical cyclization reactions with a vinylsilyl tether. Control of the reaction course by a change in the conformation of the pyranose ring due to steric repulsion between adjacent bulky protecting groups

Tetrahedron Letters ◽

10.1016/s0040-4039(99)01026-6 ◽

1999 ◽

Vol 40 (30) ◽

pp. 5527-5531 ◽

Cited By ~ 24

Author(s):

Yumi Yahiro ◽

Satoshi Ichikawa ◽

Satoshi Shuto ◽

Akira Matsuda

Keyword(s):

Radical Cyclization ◽

Protecting Groups ◽

Steric Repulsion ◽

Pyranose Ring ◽

Cyclization Reactions

ChemInform Abstract: Synthesis of C-Glycosides via Radical Cyclization Reactions with a Vinylsilyl Tether. Control of the Reaction Course by a Change in the Conformation of the Pyranose Ring due to Steric Repulsion Between Adjacent Bulky Protecting Groups

ChemInform ◽

10.1002/chin.199944225 ◽

2010 ◽

Vol 30 (44) ◽

pp. no-no

Author(s):

Yumi Yahiro ◽

Satoshi Ichikawa ◽

Satoshi Shuto ◽

Akira Matsuda

Keyword(s):

Radical Cyclization ◽

Protecting Groups ◽

Steric Repulsion ◽

Pyranose Ring ◽

Cyclization Reactions

Efficient synthesis of β-C-glucosides via radical cyclization with a silicon tether based on the conformational restriction strategy

Tetrahedron Letters ◽

10.1016/j.tetlet.2005.07.087 ◽

2005 ◽

Vol 46 (38) ◽

pp. 6555-6558 ◽

Cited By ~ 7

Author(s):

Masaru Terauchi ◽

Akira Matsuda ◽

Satoshi Shuto

Keyword(s):

Radical Cyclization ◽

Efficient Synthesis ◽

ChemInform Abstract: Nucleosides and Nucleotides. Part 190. The First Synthesis of Herbicidin B. Stereoselective Construction of the Tricyclic Undecose Moiety by a Conformational Restriction Strategy Using Steric Repulsion Between Adjacent Bulky Silyl Pro

ChemInform ◽

10.1002/chin.200007220 ◽

2010 ◽

Vol 31 (7) ◽

pp. no-no

Author(s):

Satoshi Ichikawa ◽

Satoshi Shuto ◽

Akira Matsuda

Keyword(s):

Steric Repulsion ◽

Regioselective Synthesis of 2,3‐Dihydrobenzo[ f ]isoindolones via Ag‐Catalyzed Sequential Ugi 4CR/Cascade Radical Cyclization Reaction

Advanced Synthesis & Catalysis ◽

10.1002/adsc.202001255 ◽

2021 ◽

Vol 363 (4) ◽

pp. 1038-1043

Author(s):

Ying‐Chun He ◽

Yan‐Mei Yan ◽

Zhen‐Xing Ren ◽

Yong‐Zhao Wang ◽

Qiang Yu ◽

...

Keyword(s):

Radical Cyclization ◽

Cyclization Reaction ◽

Regioselective Synthesis

Rapid construction of the 6/6/5 tricyclic framework via a tandem radical cyclization reaction and its application to the synthesis of 5-epi-7-deoxy-isoabietenin A

Organic Chemistry Frontiers ◽

10.1039/c7qo00550d ◽

2017 ◽

Vol 4 (11) ◽

pp. 2211-2215 ◽

Cited By ~ 8

Author(s):

Hao Zhang ◽

Shiqiang Ma ◽

Zhimin Xing ◽

Lin Liu ◽

Bowen Fang ◽

...

Keyword(s):

Natural Products ◽

Radical Cyclization ◽

Cyclization Reaction ◽

Rapid Construction

A tandem radical cyclization towards the 6/6/5 tricyclic skeleton, which exists in numerous natural products, was developed in modest to good yields.

Stereochemical control in radical cyclization routes to N-glycosides: role of protecting groups and of the configuration (E versus Z) of the acceptors

Tetrahedron Asymmetry ◽

10.1016/j.tetasy.2003.07.013 ◽

2003 ◽

Vol 14 (19) ◽

pp. 2939-2959 ◽

Cited By ~ 5

Author(s):

Jong Uk Rhee ◽

Brian I. Bliss ◽

T.V. RajanBabu

Keyword(s):

Radical Cyclization ◽

Protecting Groups ◽

Stereochemical Control