The Preparation and Lithiation of 3,3-Diphenyl-1,1,2-tribromocyclopropane

DOI: 10.1016/0040-4039(95)01852-9

Source and publish data:

Tetrahedron Letters p. 8573 - 8576 (1995)

Update date:2022-08-02

Topics: Preparation Lithiation

Authors:

Li, Gang

Warner, Philip M.

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/0040-4039(95)01852-9

3,3-Diphenyl-1,1,2-tribromocyclopropane 4 was synthesized from benzophenone in three steps in an overall yield of 11.4percent.Treatment of 4 with buthyllithium in THF at low temperatures, generated 1-lithio- and 1,2-dilithiocyclopropenes which were charac

Full text of DOI:10.1016/0040-4039(95)01852-9

Products guided by the article

Product name:(3,3-Diphenyl-1-cyclopropen-1-yl)(trimethyl)silane

Cas No:173595-34-1

R&D Labs maybe for 173595-34-1

MedicalChem(Yancheng)Manuf.Co.,Ltd.

Contact:+86-515-84383366

Address:Touzeng BinHai, YanCheng City, JiangSu Province, China
Hangzhou Kai Peng Biotechnology Co., Ltd.

Contact:86-571-89939007

Address:NO. 499, Wensan West Road, Xihu District, Hangzhou, 310012, China
Wuxi Innopal International Trade CO.,LTD

Contact:+86-510-80711901-8003

Address:Room 402,Building 5,Longze Garden,No.17,South huanjiu Road,Yixing City, Jiangsu,China
Chongqing Yawei Fine Chemical Co.,Ltd

Contact:0086-23-62849407

Address:Ziyou village, Nanquan town, Banan district, Chongqing China
Changsha Nutritopper Bio Technology Co.,Ltd.

Contact:+86-731-87803543

Address:East 1st Street, Baima Road, Ningxiang County

Relevant to this article

Chiral Acylsilanes in Organic Synthesis. Part 2). The Role of the Solvent, the Organometallic Reagent, and the Nature of the Substrate for the Diastereoselectivity of 1,2-Additions to Racemic Alkoxymethyl-Substituted Acylsilanes

Doi:10.1002/hlca.19930760507
(1993)
Synthesis of glycosyl chlorides with acid-labile protecting groups

Doi:10.1016/0040-4039(96)01006-4
(1996)
Rhodium-Catalyzed Carbene Transfer Reactions for Sigmatropic Rearrangement Reactions of Selenium Ylides

Doi:10.1021/acs.orglett.9b01092
(2019)
Oxidative Addition of Group 14 Element Hydrido Compounds to OsH₂(η²-CH₂=CHEt)-(CO)(PⁱPr ₃)₂: Synthesis and Characterization of the First Trihydrido-Silyl, Trihydrido-Germyl, and Trihydrido-Stannyl Derivatives of Osmium(IV)

Doi:10.1021/ic9509591
(1996)
Chlorodeoxy derivatives from D-galactochloralose

Doi:10.1016/0008-6215(95)00317-7
(1996)
Synthesis, insecticidal and anti-acetylcholinesterase activity of a new class of heterocyclic methanesulfonates

Doi:10.1016/0960-894X(95)00562-8
(1996)

Article Doi