Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Koreaki Imura"'
Publikováno v:
Tetrahedron Letters. 47:6673-6676
Two optional routes to β-phenylnaphthalene structure are developed by introducing α- and β-styryl groups onto different positions in the benzocyclobutene ring followed by ring enlargement.
Publikováno v:
Organic Letters. 4:1675-1678
[reaction: see text] The stereochemistry of the thermal conversion of alkenylbenzocyclobutenol into dihydronaphthalene was studied. Experiments on the substrates IV, in which two oxy functions are cis, often resulted in the formation of abnormal prod
Publikováno v:
Organic Letters. 6(15):2503-2505
[reaction: see text] Concise synthesis of defucogilvocarcin M was achieved via the [2 + 2 + 2] approach to beta-phenylnaphthalene structure.
Autor:
Yoriko Ohashi, Ken Ohmori, Keisuke Suzuki, Shin Futagami, Takamitsu Hosoya, Koreaki Imura, Takashi Matsumoto
Publikováno v:
ChemInform. 31
First total synthesis of ravidomycin has been achieved, thereby establishing the relative and absolute stereostructure as 1.
Publikováno v:
ChemInform. 33
The stereochemistry of the thermal conversion of alkenylbenzocyclobutenol into dihydronaphthalene was studied. Experiments on the substrates IV, in which two oxy functions are cis, often resulted in the formation of abnormal products in view of the o
Autor:
Yoriko Ohashi, Takamitsu Hosoya, Ken Ohmori, Koreaki Imura, Shin Futagami, Keisuke Suzuki, Takashi Matsumoto
Publikováno v:
Tetrahedron Letters. 41(7):1063
First total synthesis of ravidomycin has been achieved, thereby establishing the relative and absolute stereostructure as 1.