References
- Greene , T. W. and Wuts , P. G.M. 1991 . Protecting Groups in Organic Synthesis , 2nd Ed. New York : Wiley‐Interscience .
- Overman , L. and Sharp , M. J. 1988 . Enantioselective total synthesis of the aumiliotoxin A alkaloids via reductive iminium ion‐alkyne cyclizations . Tetrahedron Lett. , 29 : 901 – 905 .
- Srinath , S. , Madhavan , S. and Sambasivam , G. Modified alumina catalyst, its preparation for protection of functional intermediates and nucleophilic substitutions . PCT Int. Appl., 0324591 . March 27, 2003 .
- Kawada , K. , Watanabe , M. , Okamoto , K. , Sugihara , H. , Hirata , T. , Maki , Y. , Imada , I. and Sanno , Y. 1984 . Spirocyclopropane compounds. III. Synthesis of spiro[benzofuran‐2(3H), 1′‐cyclopropan]‐3‐ones for evaluation as gastric antisecretory and antiulcer agents . Chem. Pharm. Bull. , 32 : 3532 – 3520 . [PUBMED] [INFOTRIEVE]
- Yoshikawa , M. , Yamada , Y. M.A. , Das , J. , Sasai , H. and Shibasaki , M. 1999 . Direct catalytic asymmetric aldol reaction . J. Am. Chem. Soc. , 121 : 4168 – 4178 . [CROSSREF]
- Hanka , L. J. , Dietz , A. , Gerpheide , S. A. , Kuentzel , S. L. and Martin , D. G. 1978 . CC‐1065 (NSC‐298223), a new antitumor antibiotic. Production in‐vivo biological activity, microbiological assays, and taxonomy of the producing microorganism . J. Antibiot. , 31 : 1211 – 1217 . [PUBMED] [INFOTRIEVE]
- Ichimura , M. , Ogawa , T. , Takahashi , K. , Kobayashi , E. E. , Kawamoto , I. , Yasuzawa , T. , Takahashi , I. and Nakano , H. 1990 . A new antibiotic from Streptomyces sp. . J. Antibiot. , 43 : 1037 – 1038 . [PUBMED] [INFOTRIEVE]
- Boger , D. L. , Han , N. , Tarby , C. M. , Boyce , C. W. , Cai , H. , Jin , Q. and Kitos , P. A. 1996 . Synthesis, chemical properties, and preliminary evaluation of substituted CBI analogs of CC‐1065 and the duocarmycins incorporating the 7‐cyano‐1,2,9,9a‐tetrahydrocyclopropa[c]benz[e]indol‐4‐one alkylation subunit: hammett quantitation of the magnitude of electronic effects on functional reactivity . J. Org. Chem. , 61 : 4894 – 4912 . [CROSSREF]
- Howard , T. T. , Lingerfelt , B. M. , Purnell , B. L. , Scott , A. E. , Price , C. A. , Townes , H. M. , McNulty , L. , Handl , H. L. , Summerville , K. , Hudson , S. J. , Bowen , J. P. , Kiakos , K. , Hartley , J. A. and Lee , M. 2002 . Novel Furano analogs of duocarmycin C1 and C2: design, synthesis and biological evaluation of seco‐iso‐cyclopropylfurano[e]indoline (seco‐iso‐CFI) and the unexpected seco‐cyclopropyltetrahydrofurano[f]quinoline (seco‐CFQ) analogs . Bioorg. Med. Chem. , 10 : 2941 – 2952 . [PUBMED] [INFOTRIEVE] [CROSSREF]
- Aristoff , P. A. and Johnson , P. D. 1992 . Synthesis of CBI‐PDE‐I dimer, the benzannelated analogue of CC‐1065 . J. Org. Chem. , 75 : 6234 – 6239 .
- 2003 . Aldrich Handbook for Fine Chemicals and Laboratory Equipment Milwaukee, WI : Lane, C. President, Sigma‐Aldrich . Catalog number for N‐benzylaniline is 12,893‐7