| dc.contributor.author | Myers, Andrew | |
| dc.contributor.author | Subramanian, Vijaya | |
| dc.contributor.author | Hammond, Marlys | |
| dc.date.accessioned | 2009-06-22T20:28:13Z | |
| dc.date.issued | 1995 | |
| dc.identifier.citation | Myers, Andrew G., Vijaya Subramanian and Marlys Hammond. 1995. A concise synthesis of the naphthoic acid component of neocarzinostatin chromophore featuring a new photocyclization reaction. Tetrahedron Letters 37(5): 587-590. | en |
| dc.identifier.issn | 0040-4039 | en |
| dc.identifier.uri | http://nrs.harvard.edu/urn-3:HUL.InstRepos:3119446 | |
| dc.description.abstract | A 6-step synthesis of the naphthoic acid component of the natural antitumor agent neocarzinostatin chromophore is described. The synthetic route employs a 4-bromo-3-methylanisole as the starting material, proceeds in 31-37% yield for the 6 steps, and features as the key step a photocyclization reaction that is an interesting variant of known photocyclization reactions of stilbenes and phenylbutadienes. | en |
| dc.description.sponsorship | Chemistry and Chemical Biology | en |
| dc.language.iso | en_US | en |
| dc.publisher | Elsevier | en |
| dc.relation.isversionof | http://dx.doi.org/10.1016/0040-4039(95)02268-6 | en |
| dc.relation.hasversion | http://www.chem.harvard.edu/groups/myers/publications.htm | en |
| dash.license | META_ONLY | |
| dc.subject | chromophore | en |
| dc.subject | naphthoic acid | en |
| dc.subject | neocarzinostatin | en |
| dc.subject | photocyclization | en |
| dc.title | A Concise Synthesis of the Naphthoic Acid Component of Neocarzinostatin Chromophore Featuring a New Photocyclization Reaction | en |
| dc.type | Journal Article | |
| dc.description.version | Version of Record | |
| dc.relation.journal | Tetrahedron Letters | en |
| dash.depositing.author | Myers, Andrew | |
| dash.embargo.until | 10000-01-01 | |
| dc.identifier.doi | 10.1016/0040-4039(95)02268-6 | * |
| dash.contributor.affiliated | Myers, Andrew | |
