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Cyclobutanes

Known as: Cyclobutane, Cyclobutanes [Chemical/Ingredient] 
Four carbon cycloparaffin cyclobutane (the structural formula (CH2)4) and its derivatives.
National Institutes of Health

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50 relations

Narrower (46)

1,3-diphosphacyclobutane-2,4-diyl1,3-disilacyclobutane1-amino-3-fluoromethylcyclobutane-1-carboxylic acid1-bromosilacyclobutane
In Bloodagonistsantagonists & inhibitorschemical synthesis

Papers overview

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Highly Cited
2003
Highly Cited
2003
Sequence context-dependent replication of DNA templates containing UV-induced lesions by human DNA polymerase iota.
Highly Cited
2000
Highly Cited
2000
Electrospray-mass spectrometry characterization and measurement of far-UV-induced thymine photoproducts.
Highly Cited
1996
Highly Cited
1996
Mutation spectra of M13 vectors containing site-specific Cis-Syn, Trans-Syn-I, (6-4), and Dewar pyrimidone photoproducts of thymidylyl-(3'-->5')-thymidine in Escherichia coli under SOS conditions.
The mutations spectra of cis-syn, trans-syn-I, (6-4), and Dewar pyrimidone photoproducts of the TT site of AATTAA and TATTAT in… 
1996
1996
Comparison of the rate of excision of major UV photoproducts in the strands of the human HPRT gene of normal and xeroderma pigmentosum variant cells.
Highly Cited
1994
Highly Cited
1994
Removal of UV-induced DNA lesions in mouse epidermis soon after irradiation.
Highly Cited
1987
Highly Cited
1987
Mechanism of damage recognition by Escherichia coli DNA photolyase.
Review
1986
Review
1986
The role of the (6-4) photoproduct in ultraviolet light-induced transition mutations in E. coli.
Highly Cited
1982
Highly Cited
1982
Alkaline lability of fluorescent photoproducts produced in ultraviolet light-irradiated DNA.
Highly Cited
1972
Highly Cited
1972
PHOTOCHEMICAL REACTIONS OF AROMATIC KETONES WITH NUCLEIC ACIDS AND THEIR COMPONENTS I—. PURINE AND PYRIMIDINE BASES AND NUCLEOSIDES * .
Abstract— The photochemical reactions of benzophenone and acetophenone with purine and pyrimidine derivatives in aqueous… 
1968
1968
Trans-syn thymine dimers in ultraviolet-irradiated denatured DNA: identification and photoreactivability.
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