Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Kazumasa, Kanda"'
Autor:
Toshiyuki Goto, Shuhei Torii, Aoi Kondo, Kazumasa Kanda, Junji Kawakami, Yosky Kataoka, Takahito Nishikata
Publikováno v:
Journal of Developmental Biology, Vol 10, Iss 1, p 10 (2022)
In many animal species, the body axis is determined by the relocalization of maternal determinants, organelles, or unique cell populations in a cytoskeleton-dependent manner. In the ascidian first cell cycle, the myoplasm, including mitochondria, end
Externí odkaz:
https://doaj.org/article/9fdd5237136a4990b4dbb078d0b02b9e
Autor:
Toshiyuki Goto, Shuhei Torii, Aoi Kondo, Kazumasa Kanda, Junji Kawakami, Yosky Kataoka, Takahito Nishikata
Publikováno v:
Journal of Developmental Biology; Volume 10; Issue 1; Pages: 10
In many animal species, the body axis is determined by the relocalization of maternal determinants, organelles, or unique cell populations in a cytoskeleton-dependent manner. In the ascidian first cell cycle, the myoplasm, including mitochondria, end
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2a26ffde157ac0a3c246456b36bea30
https://pubmed.ncbi.nlm.nih.gov/35225963
https://pubmed.ncbi.nlm.nih.gov/35225963
Publikováno v:
Developmental Biology. 448:161-172
In the first ascidian cell cycle, cytoplasmic and cortical reorganization is required for distributing maternal factors to their appropriate positions, resulting in the formation of the embryonic axis. This cytoplasmic reorganization is considered to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c17798d6866a5a7814c50ebecd219ac9
https://doi.org/10.1016/j.ydbio.2018.10.014
https://doi.org/10.1016/j.ydbio.2018.10.014
Publikováno v:
Tetrahedron. 68:1407-1416
The asymmetric induction of planar chirality in 1,n-dioxa[n]paracyclophane derivatives via asymmetric ortho-lithiation is described. Enantioselective ortho-lithiation of unflippable 1,n-dioxa[n]paracyclophanes (n≤11) using sec-BuLi-(−)-sparteine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68a38894b0082d880e2008afe816e777
https://doi.org/10.1016/j.tet.2011.12.031
https://doi.org/10.1016/j.tet.2011.12.031
Publikováno v:
The Journal of Organic Chemistry. 72:6521-6525
The enantioselective intramolecular [2 + 2 + 2] cycloaddition of various enediynes, where two acetylenic moieties are connected by a trans-olefinic moiety, gave chiral tricyclic cyclohexa-1,3-dienes using Rh-H8-BINAP catalyst. In the case of carbon-a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed8177e728f12d8d6b7f78f6c9ed382c
https://doi.org/10.1021/jo070762d
https://doi.org/10.1021/jo070762d
Publikováno v:
ChemInform. 45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5ddec3be3737e7e20a9c41bed50a74e
https://doi.org/10.1002/chin.201421026
https://doi.org/10.1002/chin.201421026
Autor:
Mamoru, Ishii, Shoichi, Okano, Eiichi, Sagawa, Shin'ichi, Watari, Hirotaka, Mori, Iwao, Iwamoto, Kazumasa, Kanda, Fumihiko, Kamimura, Dai, Sakamoto
Publikováno v:
Advances in polar upper atmosphere research. 15:178-192
The importance of automatic observation systems for ground-based optical instruments is increasing since clustered measurements are being made with only a few operators. We have developed an automatic observation system for use with both a scanning a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=jairo_______::13ed386e11e78a283bf76a57e756a3a6
http://id.nii.ac.jp/1291/00006339/
http://id.nii.ac.jp/1291/00006339/
Publikováno v:
Organic letters. 12(9)
Highly enantioselective ortho-lithiation and dilithiation of 1,n-dioxa[n]paracyclophanes were realized with the use of sec-butyllithium and a catalytic or stoichiometric amount of sparteine. Quenching with various electrophiles, such as iodine, iodom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e78d07c2a3a9c6f37185980791b49c0
https://pubmed.ncbi.nlm.nih.gov/20349947
https://pubmed.ncbi.nlm.nih.gov/20349947
Publikováno v:
ChemInform. 40
The double Sonogashira coupling of diiodoparacyclophanes with alkynes proceeded to give planarly chiral dialkynylparacyclophanes; a chiral Pd catalyst, which was prepared in situ from PdCl2(CH3CN)2 and Taniaphos, realized the first asymmetric Sonogas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd66a7cee1616c7719fc06dcfed99c9f
https://doi.org/10.1002/chin.200935170
https://doi.org/10.1002/chin.200935170
Publikováno v:
ChemInform. 39
The enantioselective intramolecular [2 + 2 + 2] cycloaddition of various enediynes, where two acetylenic moieties are connected by a trans-olefinic moiety, gave chiral tricyclic cyclohexa-1,3-dienes using Rh-H8-BINAP catalyst. In the case of carbon-a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae6ae1813cd5eb04c9ab7f36eae85a78
https://doi.org/10.1002/chin.200802031
https://doi.org/10.1002/chin.200802031