1![Department of Chemistry Jennifer Schloss Mentor: Dina Merrer Mechanism of Halocarbene Additions to Cyclooctyne Cyclooctyne (1) was successfully synthesized and purified from cis-cyclooctene (10) via 1bromocyclooctene (1 Department of Chemistry Jennifer Schloss Mentor: Dina Merrer Mechanism of Halocarbene Additions to Cyclooctyne Cyclooctyne (1) was successfully synthesized and purified from cis-cyclooctene (10) via 1bromocyclooctene (1](https://www.pdfsearch.io/img/1a0cb2f917c695455bc954a85172586e.jpg) | Add to Reading ListSource URL: barnard.eduLanguage: English - Date: 2011-10-20 14:33:04
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2![Department of Chemistry Denise Napolitano Mentor: Dr. Dina C. Merrer Mechanisms of Halocarbene Additions to Cyclooctyne The additions of dichlorocarbene (2a) and phenylhalocarbenes (2b, 2c) to cyclooctyne 1 Department of Chemistry Denise Napolitano Mentor: Dr. Dina C. Merrer Mechanisms of Halocarbene Additions to Cyclooctyne The additions of dichlorocarbene (2a) and phenylhalocarbenes (2b, 2c) to cyclooctyne 1](https://www.pdfsearch.io/img/9153648e3ec34275e30e9912bd05f0d8.jpg) | Add to Reading ListSource URL: barnard.edu- Date: 2011-10-20 15:13:58
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3![Department of Chemistry Marlena Sheridan Mentor: Dina Merrer Mechanism of Addition of Dihalocarbenes to Cycloheptyne and 3,3-Difluorocyclooctyne Department of Chemistry Marlena Sheridan Mentor: Dina Merrer Mechanism of Addition of Dihalocarbenes to Cycloheptyne and 3,3-Difluorocyclooctyne](https://www.pdfsearch.io/img/318e92c735cbfb8981d9edbe0ef349ab.jpg) | Add to Reading ListSource URL: barnard.eduLanguage: English - Date: 2011-10-04 12:45:35
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4![Department of Chemistry Kaitlyn Suski Mentor: Dina Merrer Reactivity of Dihalocarbenes with Cycloalkyne Cyclooctyne (1) was successfully synthesized and purified, and was reacted with dibromo- and dichlorocarbene (:CX2, Department of Chemistry Kaitlyn Suski Mentor: Dina Merrer Reactivity of Dihalocarbenes with Cycloalkyne Cyclooctyne (1) was successfully synthesized and purified, and was reacted with dibromo- and dichlorocarbene (:CX2,](https://www.pdfsearch.io/img/a5e5cd11c541a66ba64d0f7bb63153db.jpg) | Add to Reading ListSource URL: barnard.eduLanguage: English - Date: 2011-10-20 14:52:05
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6![http://www.orgsyn.org/orgsyn/orgsyn/prepcontent_forpdfs.asp?pri http://www.orgsyn.org/orgsyn/orgsyn/prepcontent_forpdfs.asp?pri](https://www.pdfsearch.io/img/716eb234a436836a7c0636094fbe65db.jpg) | Add to Reading ListSource URL: www.orgsyn.orgLanguage: English - Date: 2006-06-16 18:43:00
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7![http://www.orgsyn.org/orgsyn/orgsyn/prepcontent_forpdfs.asp?pri http://www.orgsyn.org/orgsyn/orgsyn/prepcontent_forpdfs.asp?pri](https://www.pdfsearch.io/img/7089d7ce2f268b79127a4f87e133d0e2.jpg) | Add to Reading ListSource URL: www.orgsyn.orgLanguage: English - Date: 2006-06-23 12:55:00
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8![carbenes The electrically neutral species H2C
and its derivatives, in which the carbon is covalently bonded to two univalent groups of any kind or a carbenes The electrically neutral species H2C
and its derivatives, in which the carbon is covalently bonded to two univalent groups of any kind or a](https://www.pdfsearch.io/img/70945a4cd37cf1484c583cab13ee9525.jpg) | Add to Reading ListSource URL: old.iupac.org- Date: 1999-08-11 14:35:55
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9![Microsoft Word - MCP030402 Microsoft Word - MCP030402](https://www.pdfsearch.io/img/a1187ce9b1e44ecb00740e2c0f03a76b.jpg) | Add to Reading ListSource URL: www.mdpi.orgLanguage: English - Date: 2006-01-30 15:51:48
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