Synthesis of branched ribofuranans and their sulfates with strong anti-AIDS virus activity by selective ring-opening copolymerization of 1,4-anhydro-α-D-ribopyranose derivatives.

1992 ◽  
Vol 25 (16) ◽  
pp. 4051-4057 ◽  
Author(s):  
Takashi Yoshida ◽  
Yoshiaki Katayama ◽  
Shoji Inoue ◽  
Toshiyuki Uryu
Keyword(s):  
Ring Opening ◽  
Virus Activity ◽  
Aids Virus ◽  
Selective Ring Opening

Synthesis of Cellulose-Type Polyriboses and Their Branched Sulfates with Anti-AIDS Virus Activity by Selective Ring-Opening Copolymerization of 1,4-Anhydro-.alpha.-D-ribopyranose Derivatives

1994 ◽  
Vol 27 (16) ◽  
pp. 4422-4428 ◽  
Author(s):  
Takashi Yoshida ◽  
Chengpei Wu ◽  
Lixin Song ◽  
Toshiyuki Uryu ◽  
Yutaro Kaneko ◽  
...  
Keyword(s):  
Ring Opening ◽  
Virus Activity ◽  
Aids Virus ◽  
Selective Ring Opening

Synthesis of sulfated octadecyl ribo-oligosaccharides with potent anti-AIDS virus activity by ring-opening polymerization of a 1,4-anhydroribose derivative

1996 ◽  
Vol 282 (1) ◽  
pp. 113-123 ◽  
Author(s):  
YoonSoung Choi ◽  
Takashi Yoshida ◽  
Toru Mimura ◽  
Yutaro Kaneko ◽  
Hideki Nakashima ◽  
...  
Keyword(s):  
Ring Opening ◽  
Ring Opening Polymerization ◽  
Virus Activity ◽  
Aids Virus

scholarly journals Synthesis of Sulfated Deoxy-Ribofuranans Having Selective Anti-AIDS Virus Activity by Ring-Opening Copolymerization of 1,4-Anhydro Ribose Derivatives

1997 ◽  
Vol 29 (4) ◽  
pp. 374-379 ◽  
Author(s):  
Yoon Soung Choi ◽  
Byoung Won Kang ◽  
Rong Lu ◽  
Mitsuru Osawa ◽  
Kazuyuki Hattori ◽  
...  
Keyword(s):  
Ring Opening ◽  
Virus Activity ◽  
Aids Virus

S ‐Carboxyanhydrides: Ultrafast and Selective Ring‐Opening Polymerizations Towards Well‐defined Functionalized Polythioesters

2021 ◽  
Vol 133 (19) ◽  
pp. 10893-10900
Author(s):  
Yanchao Wang ◽  
Maosheng Li ◽  
Shixue Wang ◽  
Youhua Tao ◽  
Xianhong Wang
Keyword(s):  
Ring Opening ◽  
Selective Ring Opening

C3-Allylation of Indoles via an Iridium-Catalyzed Branch-Selective Ring-Opening Reaction of Vinylcyclopropanes

Synthesis ◽  
2018 ◽  
Vol 51 (07) ◽  
pp. 1655-1661 ◽  
Author(s):  
Guang-Jian Mei ◽  
Feng Shi ◽  
Lei Yu ◽  
Zi-Qi Zhu ◽  
Meng Sun
Keyword(s):  
Ring Opening ◽  
Economic Approach ◽  
Whole Process ◽  
Ring Opening Reaction ◽  
Selective Ring Opening

An iridium-catalyzed branch-selective ring-opening reaction of vinylcyclopropanes with indoles has been established, which afforded C3-allylindoles in generally good to excellent yields (up to 95%). Considering that no wastes were generated in the whole process and branch-selective ring-opening reaction of vinylcyclopropanes was rarely reported, this strategy not only can be regarded as a highly atom-economic approach for C3-allylindoles, but also will greatly enrich the chemistry of vinylcyclopropanes.

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