Parallel synthesis and evaluation of 132 (+)-1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indol-4-one (CBI) analogues of CC-1065 and the duocarmycins defining the contribution of the DNA-binding domain.
- DOI
- 10.1021/jo010454u
- Published
- 2001 Oct 5
- Container
- The Journal of organic chemistry
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1021/jo010454u,
title = {Parallel synthesis and evaluation of 132 (+)-1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indol-4-one (CBI) analogues of CC-1065 and the duocarmycins defining the contribution of the DNA-binding domain.},
author = {Boger DL and Schmitt HW and Fink BE and Hedrick MP},
year = {2001},
journal = {The Journal of organic chemistry},
doi = {10.1021/jo010454u},
url = {https://doi.org/10.1021/jo010454u}
}RIS
TY - JOUR TI - Parallel synthesis and evaluation of 132 (+)-1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indol-4-one (CBI) analogues of CC-1065 and the duocarmycins defining the contribution of the DNA-binding domain. AU - Boger DL AU - Schmitt HW AU - Fink BE AU - Hedrick MP PY - 2001 JO - The Journal of organic chemistry DO - 10.1021/jo010454u UR - https://doi.org/10.1021/jo010454u ER -
APA
DL, B., HW, S., BE, F., & MP, H. (2001). Parallel synthesis and evaluation of 132 (+)-1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indol-4-one (CBI) analogues of CC-1065 and the duocarmycins defining the contribution of the DNA-binding domain.. The Journal of organic chemistry. https://doi.org/10.1021/jo010454u
Source records
- pubmed · retrieved 2026-09-27T00:08:54.435Z