JPH0440335B2 - - Google Patents

Info

Publication number
JPH0440335B2
JPH0440335B2 JP60044619A JP4461985A JPH0440335B2 JP H0440335 B2 JPH0440335 B2 JP H0440335B2 JP 60044619 A JP60044619 A JP 60044619A JP 4461985 A JP4461985 A JP 4461985A JP H0440335 B2 JPH0440335 B2 JP H0440335B2
Authority
JP
Japan
Prior art keywords
reaction
ether
group
represented
mmol
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP60044619A
Other languages
English (en)
Japanese (ja)
Other versions
JPS61205222A (ja
Inventor
Masakatsu Shibazaki
Atsuo Takahashi
Mikiko Sodeoka
Masayuki Yokota
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sagami Chemical Research Institute
Original Assignee
Sagami Chemical Research Institute
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sagami Chemical Research Institute filed Critical Sagami Chemical Research Institute
Priority to JP60044619A priority Critical patent/JPS61205222A/ja
Publication of JPS61205222A publication Critical patent/JPS61205222A/ja
Publication of JPH0440335B2 publication Critical patent/JPH0440335B2/ja
Granted legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Pyrane Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
JP60044619A 1985-03-08 1985-03-08 シス−ビシクロ〔3.3.0〕オクチリデン誘導体 Granted JPS61205222A (ja)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60044619A JPS61205222A (ja) 1985-03-08 1985-03-08 シス−ビシクロ〔3.3.0〕オクチリデン誘導体

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60044619A JPS61205222A (ja) 1985-03-08 1985-03-08 シス−ビシクロ〔3.3.0〕オクチリデン誘導体

Publications (2)

Publication Number Publication Date
JPS61205222A JPS61205222A (ja) 1986-09-11
JPH0440335B2 true JPH0440335B2 (cs) 1992-07-02

Family

ID=12696448

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60044619A Granted JPS61205222A (ja) 1985-03-08 1985-03-08 シス−ビシクロ〔3.3.0〕オクチリデン誘導体

Country Status (1)

Country Link
JP (1) JPS61205222A (cs)

Also Published As

Publication number Publication date
JPS61205222A (ja) 1986-09-11

Similar Documents

Publication Publication Date Title
Marshall et al. Synthetic studies on cembranolides. Stereoselective synthesis of a crassin acetate synthon
AU634213B2 (en) Preparation of 5,6,7-trinor-4,8-inter-m-phenylene pgi2 derivatives
Corey et al. Biomimetic synthesis of a preclavulone a model
Schaaf et al. Total synthesis of prostaglandins F1. alpha. and E1
Welch et al. Stereoselective total syntheses of (+-)-longicyclene,(+-)-longicamphor, and (+-)-longiborneol
Ziegler et al. Synthesis of the 1, 3-dioxolane ring system of the trichothecenes sambucinol and sporol via a stereoselective Claisen rearrangement
Caine et al. Synthesis and photochemical rearrangement of (1 (R), 7a (S))-1-(tert-butyldiphenylsiloxy)-7a-methyl-5 (7aH)-indanone
JPH0440335B2 (cs)
US5886233A (en) Cyclohexanone derivatives, process for their production and intermediate products of the process
Nemoto et al. Ring expansion of cyclopropylmethanols to cyclobutanes—an enantioselective total synthesis of (R)-(+)-dodecan-5-olide, and (S)-(+)-and (R)-(–)-5-[(Z)-dec-1-enyl] dihydrofuran-2 (3H)-one
JPH05974A (ja) ハロゲン化不飽和アルキル化合物及びその前駆体
Sirat et al. A fragmentation approach to a maytansine synthon: lithium dimethylcuprate-opening of substituted cyclohexene epoxides. X-Ray structure determination of ethyl t-2, 3-epoxy-c-6-p-methoxybenzoyloxy-1-methylcyclohexane-r-1-carboxylate
US4535179A (en) Synthesis of bicyclic and tricyclic 7-oxa prostaglandin endoperoxide analogs via oxypalladation of norbornadiene
Daniewski et al. Synthesis of the Ring d‐Building Block of (24S)‐24‐Hydroxy Vitamin D3 from Menthol, I
JP3353619B2 (ja) アシルオキシケトンの製造法
JPH0472835B2 (cs)
EP0008951B1 (en) Steroid intermediate, method for production thereof, and method for producing another steroid intermediate therefrom
JPH0558425B2 (cs)
Nizovtsev et al. Unusual selectivity in the oxidative functionalization of gem-dibromocyclopropanes
JPH07242595A (ja) α−フルオロシクロアルケノン類の製造方法
JPS632251B2 (cs)
FR2537578A1 (fr) Procede de preparation de trichloromethyl-carbinols
JPH0118888B2 (cs)
JPH07242577A (ja) 光学活性シクロプロパン誘導体
KOYAMA et al. Synthesis of a bicyclo [3.2. 1] octane analogue of isocarbacyclin