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Regiodivergent synthesis of functionalized indene derivatives via Pt-catalyzed Rautenstrauch reaction of propargyl carbonates.
Org Lett. 2012 Apr 06; 14(7):1668-71.OL

Abstract

A regiodivergent synthesis of functionalized indene derivatives from a Pt-catalyzed Rautenstrauch reaction of propargyl carbonate is described. A one-pot Rautenstrauch/Tsuji-Trost reaction delivering 2-indanones was realized efficiently using this methodology.

Authors+Show Affiliations

1-014 Center for Science and Technology, Department of Chemistry, Syracuse University, Syracuse, New York 13244, USA.No affiliation info available

Pub Type(s)

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

Language

eng

PubMed ID

22416889

Citation

Zhao, Jinbo, and Daniel A. Clark. "Regiodivergent Synthesis of Functionalized Indene Derivatives Via Pt-catalyzed Rautenstrauch Reaction of Propargyl Carbonates." Organic Letters, vol. 14, no. 7, 2012, pp. 1668-71.
Zhao J, Clark DA. Regiodivergent synthesis of functionalized indene derivatives via Pt-catalyzed Rautenstrauch reaction of propargyl carbonates. Org Lett. 2012;14(7):1668-71.
Zhao, J., & Clark, D. A. (2012). Regiodivergent synthesis of functionalized indene derivatives via Pt-catalyzed Rautenstrauch reaction of propargyl carbonates. Organic Letters, 14(7), 1668-71. https://doi.org/10.1021/ol300158d
Zhao J, Clark DA. Regiodivergent Synthesis of Functionalized Indene Derivatives Via Pt-catalyzed Rautenstrauch Reaction of Propargyl Carbonates. Org Lett. 2012 Apr 6;14(7):1668-71. PubMed PMID: 22416889.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Regiodivergent synthesis of functionalized indene derivatives via Pt-catalyzed Rautenstrauch reaction of propargyl carbonates. AU - Zhao,Jinbo, AU - Clark,Daniel A, Y1 - 2012/03/14/ PY - 2012/3/16/entrez PY - 2012/3/16/pubmed PY - 2012/6/21/medline SP - 1668 EP - 71 JF - Organic letters JO - Org Lett VL - 14 IS - 7 N2 - A regiodivergent synthesis of functionalized indene derivatives from a Pt-catalyzed Rautenstrauch reaction of propargyl carbonate is described. A one-pot Rautenstrauch/Tsuji-Trost reaction delivering 2-indanones was realized efficiently using this methodology. SN - 1523-7052 UR - https://www.unboundmedicine.com/medline/citation/22416889/Regiodivergent_synthesis_of_functionalized_indene_derivatives_via_Pt_catalyzed_Rautenstrauch_reaction_of_propargyl_carbonates_ L2 - https://doi.org/10.1021/ol300158d DB - PRIME DP - Unbound Medicine ER -