The intramolecular meta-photocycloaddition of bichromophores 1a and 1b is examined and the observed stereochemistry of cycloaddition is rationalized in terms of hydrogen bond effect introduced by the 3-hydroxy group in the 5-phenylpent-1-ene skeleton.
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LANZHOU UNIV,INST ORGAN CHEM,NATL LAB APPL ORGAN CHEM,LANZHOU 730000,PEOPLES R CHINALANZHOU UNIV,INST ORGAN CHEM,NATL LAB APPL ORGAN CHEM,LANZHOU 730000,PEOPLES R CHINA
Zhang, C
Guo, XC
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LANZHOU UNIV,INST ORGAN CHEM,NATL LAB APPL ORGAN CHEM,LANZHOU 730000,PEOPLES R CHINALANZHOU UNIV,INST ORGAN CHEM,NATL LAB APPL ORGAN CHEM,LANZHOU 730000,PEOPLES R CHINA
Guo, XC
Shen, XM
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LANZHOU UNIV,INST ORGAN CHEM,NATL LAB APPL ORGAN CHEM,LANZHOU 730000,PEOPLES R CHINALANZHOU UNIV,INST ORGAN CHEM,NATL LAB APPL ORGAN CHEM,LANZHOU 730000,PEOPLES R CHINA
机构:
Chinese Acad Sci, Shanghai Inst Organ Chem, Lab Organofluorine Chem, Shanghai 200032, Peoples R ChinaChinese Acad Sci, Shanghai Inst Organ Chem, Lab Organofluorine Chem, Shanghai 200032, Peoples R China
Guo, XC
Chen, QY
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Chinese Acad Sci, Shanghai Inst Organ Chem, Lab Organofluorine Chem, Shanghai 200032, Peoples R ChinaChinese Acad Sci, Shanghai Inst Organ Chem, Lab Organofluorine Chem, Shanghai 200032, Peoples R China