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Palladium-catalyzed highly regioselective [3 + 2] cycloaddition reactions of alkylidenecyclopropa[b]naphthalenes with alkenes or alkynes: an efficient synthesis of 1(3)-alkylidene-2,3-dihydro-1H-benzo[f]indenes and 1-alkylidene-1H-benzo[f]indenes.
Org Lett. 2008 Dec 18; 10(24):5537-40.OL

Abstract

The first palladium-catalyzed highly regioselective [3 + 2] cycloaddition reactions of alkylidenecyclopropa[b]naphthalenes 1 with alkenes or alkynes is presented, providing an efficient method for the synthesis of 1(3)-alkylidene-2,3-dihydro-1H-benzo[f]indenes or 1-alkylidene-1H-benzo[f]indenes under mild conditions.

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Publisher Full Text (DOI)

Authors+Show Affiliations

Chen W
Center of Analysis & Measurement, Zhejiang University of Technology, Hangzhou 310014, PR China.
Cao J
No affiliation info available
Huang X
No affiliation info available

MeSH

AlkenesAlkynesCatalysisCyclizationIndenesNaphthalenesPalladium

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

19053725

Citation

Chen, Wanli, et al. "Palladium-catalyzed Highly Regioselective [3 + 2] Cycloaddition Reactions of Alkylidenecyclopropa[b]naphthalenes With Alkenes or Alkynes: an Efficient Synthesis of 1(3)-alkylidene-2,3-dihydro-1H-benzo[f]indenes and 1-alkylidene-1H-benzo[f]indenes." Organic Letters, vol. 10, no. 24, 2008, pp. 5537-40.
Chen W, Cao J, Huang X. Palladium-catalyzed highly regioselective [3 + 2] cycloaddition reactions of alkylidenecyclopropa[b]naphthalenes with alkenes or alkynes: an efficient synthesis of 1(3)-alkylidene-2,3-dihydro-1H-benzo[f]indenes and 1-alkylidene-1H-benzo[f]indenes. Org Lett. 2008;10(24):5537-40.
Chen, W., Cao, J., & Huang, X. (2008). Palladium-catalyzed highly regioselective [3 + 2] cycloaddition reactions of alkylidenecyclopropa[b]naphthalenes with alkenes or alkynes: an efficient synthesis of 1(3)-alkylidene-2,3-dihydro-1H-benzo[f]indenes and 1-alkylidene-1H-benzo[f]indenes. Organic Letters, 10(24), 5537-40. https://doi.org/10.1021/ol8023083
Chen W, Cao J, Huang X. Palladium-catalyzed Highly Regioselective [3 + 2] Cycloaddition Reactions of Alkylidenecyclopropa[b]naphthalenes With Alkenes or Alkynes: an Efficient Synthesis of 1(3)-alkylidene-2,3-dihydro-1H-benzo[f]indenes and 1-alkylidene-1H-benzo[f]indenes. Org Lett. 2008 Dec 18;10(24):5537-40. PubMed PMID: 19053725.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Palladium-catalyzed highly regioselective [3 + 2] cycloaddition reactions of alkylidenecyclopropa[b]naphthalenes with alkenes or alkynes: an efficient synthesis of 1(3)-alkylidene-2,3-dihydro-1H-benzo[f]indenes and 1-alkylidene-1H-benzo[f]indenes. AU - Chen,Wanli, AU - Cao,Jian, AU - Huang,Xian, PY - 2008/12/5/entrez PY - 2008/12/5/pubmed PY - 2009/8/28/medline SP - 5537 EP - 40 JF - Organic letters JO - Org Lett VL - 10 IS - 24 N2 - The first palladium-catalyzed highly regioselective [3 + 2] cycloaddition reactions of alkylidenecyclopropa[b]naphthalenes 1 with alkenes or alkynes is presented, providing an efficient method for the synthesis of 1(3)-alkylidene-2,3-dihydro-1H-benzo[f]indenes or 1-alkylidene-1H-benzo[f]indenes under mild conditions. SN - 1523-7052 UR - https://www.unboundmedicine.com/medline/citation/19053725/Palladium_catalyzed_highly_regioselective_[3_+_2]_cycloaddition_reactions_of_alkylidenecyclopropa[b]naphthalenes_with_alkenes_or_alkynes:_an_efficient_synthesis_of_1_3__alkylidene_23_dihydro_1H_benzo[f]indenes_and_1_alkylidene_1H_benzo[f]indenes_ DB - PRIME DP - Unbound Medicine ER -