Bio-supramolecular photochirogenesis with molecular chaperone: enantiodifferentiating photocyclodimerization of 2-anthracenecarboxylate mediated by prefoldin

被引:20
作者
Bando, Kazuki [1 ]
Zako, Tamotsu [2 ]
Sakono, Masafumi [2 ]
Maeda, Mizuo [2 ]
Wada, Takehiko [3 ]
Nishijima, Masaki [4 ]
Fukuhara, Gaku [1 ]
Yang, Cheng [1 ,5 ]
Mori, Tadashi [1 ]
Pace, Tamara C. S. [6 ]
Bohne, Cornelia [6 ]
Inoue, Yoshihisa [1 ]
机构
[1] Osaka Univ, Dept Appl Chem, Suita, Osaka 5650871, Japan
[2] RIKEN, Bioengn Lab, 2-1 Hirosawa, Wako, Saitama 3510198, Japan
[3] Tohoku Univ, Inst Multidisciplinary Res Adv Mat, Aoba Ku, Sendai, Miyagi 9808577, Japan
[4] Osaka Univ, Ctr Adv Sci & Innovat, Suita, Osaka 5650871, Japan
[5] Osaka Univ, Dept Appl Chem, PRESTO, JST, Suita, Osaka 5650871, Japan
[6] Univ Victoria, Dept Chem, Victoria, BC V8W 3V6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
ASYMMETRIC PHOTOCHEMICAL-REACTIONS; CHIRALLY MODIFIED ZEOLITES; GROUP-II CHAPERONIN; 2+2 PHOTOCYCLOADDITION; NONNATIVE SUBSTRATE; CONFINED SPACES; TRIPLET-STATE; PHOTOISOMERIZATION; INDUCTION; PHOTOCYCLIZATION;
D O I
10.1039/b9pp00186g
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Photocyclodimerization of 2-anthracenecarboxylate mediated by molecular chaperone protein was performed for the first time to afford chiral syn-head-to-tail and anti-head-to-head dimers (2 and 3) in 10% and 16% enantiomeric excess, respectively, with enhanced yields of sterically and electrostatically less-favored head-to-head dimers (3 and 4).
引用
收藏
页码:655 / 660
页数:6
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