Showing results (21-30 of 251) with videos related to
Sort By:
Pageof 26
Acta Crystallographica. Section E, Crystallographic Communications|June 17, 2016
Crystal structure of (+)-N-[(1R,5S,6S,9S)-5-hydroxy-methyl-3,3,9-trimethyl-8-oxo-2,4,7-trioxabi-cyclo-[4.3.0]nonan-9-yl]acetamideTakeshi Oishi, Shun Tsuzaki, Tomoya Sugai, et al.Organic Letters|November 26, 2010
Novel sequential sigmatropic rearrangements of allylic diols: application to the total synthesis of (-)-kainic acidKatsunori Kitamoto, Mana Sampei, Yasuaki Nakayama, et al.Acta Crystallographica. Section E, Structure Reports Online|January 4, 2013
(+)-(1S,5R,6R)-6-[(S)-1-Hy-droxy-2-(meth-oxy-meth-yloxy)eth-yl]-1-methyl-3-trichloro-methyl-2-aza-4,7-dioxa-bicyclo-[3.3.0]oct-2-en-8-oneTakeshi Oishi, Hiroki Oishi, Syun Tsuzaki, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|April 4, 2019
Copper-Catalyzed Electrophilic Amidation of Organotrifluoroborates with Use of N-MethoxyamidesShona Banjo, Eiko Nakasuji, Tatsuhiko Meguro, et al.Chemistry, an Asian Journal|November 9, 2010
Total synthesis of (-)-salinosporamide AYuji Kaiya, Jun-ichi Hasegawa, Takayuki Momose, et al.Chemistry, an Asian Journal|May 1, 2020
Copper-Catalyzed Electrophilic Etherification of Arylboronic Esters with IsoxazolidinesSeiya Katahara, Tenga Takahashi, Kengo Nomura, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|May 28, 2014
Two-step synthesis of multi-substituted amines by using an N-methoxy group as a reactivity control elementMakoto Yoritate, Tatsuhiko Meguro, Naoya Matsuo, et al.Acta Crystallographica. Section E, Crystallographic Communications|February 13, 2016
Crystal structure of (±)-(5SR,6SR)-6-ethenyl-1-[(RS)-1-phenyl-eth-oxy]-1-aza-spiro-[4.5]decan-2-oneTakeshi Oishi, Shio Yamamoto, Takashi Yokoyama, et al.Organic Letters|November 16, 2022
Copper-Catalyzed Electrophilic Enamidation Using Dioxazolones through Hydrozirconation of AlkynesShona Banjo, Keisuke Nakata, Eiko Nakasuji, et al.Organic Letters|April 6, 2021
Five-Step Total Synthesis of (±)-Aspidospermidine by a Lactam Strategy via an Azomethine YlideSeiya Katahara, Yasukazu Sugiyama, Mina Yamane, et al.Pageof 26