Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Kusuo Horiki"'
Autor:
Kusuo Horiki
Publikováno v:
Peptide Chemistry 1992 ISBN: 9789401046480
Peptide Chemistry 1992
Peptide Chemistry 1992
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae2da5ca5448bc7fd82f72291d596b0d
https://doi.org/10.1007/978-94-011-1474-5_13
https://doi.org/10.1007/978-94-011-1474-5_13
Autor:
Kusuo Horiki, Ken'ichi Takeda
Publikováno v:
HETEROCYCLES. 30:367
Sulfenyl-transfer reactions toward a variety of nucleophiles were successfully carried out using N 3 -sulfenyl-substituted 5,5-dimethylhydantoins (2a-c). During the course of the synthesis of 2 by the reaction of N 1 -bromo-5,5-dimethyl-hydantoin (1c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22034dab52e65c6643951ed5a8ec2508
https://doi.org/10.3987/com-89-s71
https://doi.org/10.3987/com-89-s71
Peptide synthesis by means of polymer-anchored N-hydroxy compound. 1. Preparation of simple peptides
Publikováno v:
Reactive Polymers, Ion Exchangers, Sorbents. 6:127-142
6-Acetamido-1-hydroxy-3-trifluoromethylindazole ( 5 ) was incorporated into either a Merrifield bead-type chloromethylated copolystyrene with 2% divinylbenzene or a chloromethylated polystyrene-polypropylene composite fiber-type polymer to obtain 7a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f185b62e2e1f210a5cc225755fa7c0a7
https://doi.org/10.1016/0167-6989(87)90084-5
https://doi.org/10.1016/0167-6989(87)90084-5
Autor:
Kusuo Horiki
Publikováno v:
Tetrahedron Letters. 17:4103-4106
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36f7122f4212b14497f5e46072f5b2d6
https://doi.org/10.1016/s0040-4039(00)92586-3
https://doi.org/10.1016/s0040-4039(00)92586-3
Autor:
Kusuo Horiki
Publikováno v:
Synthetic Communications. 7:251-259
Several attempts for synthesis of thiol esters from carboxylic acids and thiols have been recently made with considerable success using peptide coupling reagents or related compound, which were introduced by Yamada et al.,2 Masamune et al.,3 and Muka
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f09fac57054b6d3c5f6b2ba23a9a76a
https://doi.org/10.1080/00397917708050744
https://doi.org/10.1080/00397917708050744
Autor:
Kusuo Horiki
Publikováno v:
Tetrahedron Letters. 18:1897-1900
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89edc3d8ee3310bd28c21a4f3bdb542c
https://doi.org/10.1016/s0040-4039(01)83635-2
https://doi.org/10.1016/s0040-4039(01)83635-2
Autor:
Kusuo Horiki
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 35:814-827
A number of peptide coupling reagents have been developed so far. Although some reviews on the reagents have already been appeared, this review article describes on the mechanisms of peptide coupling reactions which involve the recemization, the inte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3de77f7355cc52ba852620755fe99ca
https://doi.org/10.5059/yukigoseikyokaishi.35.814
https://doi.org/10.5059/yukigoseikyokaishi.35.814
Autor:
Kusuo Horiki
Publikováno v:
Synthetic Communications. 8:515-522
Considerable efforts to develop mild and efficient reactions and syntheses are currently being attempted by mimicking biochemical processes taking advantage of weak intermolecular forces, such as hydrophobic bonding,2 charge transfer complex formatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7632a6ab7bfa890207a110aa27f0c227
https://doi.org/10.1080/00397917808063582
https://doi.org/10.1080/00397917808063582
Publikováno v:
Chemistry Letters. 7:165-168
A synthesis of the Merrifield resin esters of N-protected amino acids was attempted with the aid of hydrogen-bonding property of fluoride ion with carboxylic acids to obtain the esters in satisfactory yields. This will provide an alternatively effici
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e0a2a5d98980c350112abcd9adb5ad0
https://doi.org/10.1246/cl.1978.165
https://doi.org/10.1246/cl.1978.165
Publikováno v:
Chemical and Pharmaceutical Bulletin. 23:2711-2727
25D-Spirosta-1, 4, 11-trien-3-one (5a) and androsta-1, 4, 11-trien-17β-ol-3-one acetate (16b) were prepared from hecogenin and 5β-androstane-3α, 12α, 17β-triol, respectively. The dienone-phenol rearrangements of these compounds were carried out
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5c90926b5e60490be77f8a321359379
https://doi.org/10.1248/cpb.23.2711
https://doi.org/10.1248/cpb.23.2711