JPS6236033B2 - - Google Patents

Info

Publication number
JPS6236033B2
JPS6236033B2 JP52055125A JP5512577A JPS6236033B2 JP S6236033 B2 JPS6236033 B2 JP S6236033B2 JP 52055125 A JP52055125 A JP 52055125A JP 5512577 A JP5512577 A JP 5512577A JP S6236033 B2 JPS6236033 B2 JP S6236033B2
Authority
JP
Japan
Prior art keywords
group
formula
chloroform
hydrogen atom
methyl
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
Application number
JP52055125A
Other languages
English (en)
Japanese (ja)
Other versions
JPS53141289A (en
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.)
Microbial Chemistry Research Foundation
Original Assignee
Microbial Chemistry Research Foundation
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 Microbial Chemistry Research Foundation filed Critical Microbial Chemistry Research Foundation
Priority to JP5512577A priority Critical patent/JPS53141289A/ja
Priority to GB7927/78A priority patent/GB1587685A/en
Priority to US05/883,301 priority patent/US4196280A/en
Priority to DE19782809598 priority patent/DE2809598A1/de
Priority to CA000298457A priority patent/CA1119588A/en
Publication of JPS53141289A publication Critical patent/JPS53141289A/ja
Priority to US06/075,036 priority patent/US4255564A/en
Publication of JPS6236033B2 publication Critical patent/JPS6236033B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Saccharide Compounds (AREA)
JP5512577A 1977-03-09 1977-05-12 Novel macrolactone compounds Granted JPS53141289A (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
JP5512577A JPS53141289A (en) 1977-05-12 1977-05-12 Novel macrolactone compounds
GB7927/78A GB1587685A (en) 1977-03-09 1978-01-28 Macrolactone derivatives and their production
US05/883,301 US4196280A (en) 1977-03-09 1978-03-03 Novel macrolactone derivatives and process of producing them
DE19782809598 DE2809598A1 (de) 1977-03-09 1978-03-06 Neue makrolactonderivate und verfahren zu ihrer herstellung
CA000298457A CA1119588A (en) 1977-03-09 1978-03-08 Process of producing novel macrolactone derivatives
US06/075,036 US4255564A (en) 1977-03-09 1979-09-12 Novel macrolactone derivatives and process of producing them

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5512577A JPS53141289A (en) 1977-05-12 1977-05-12 Novel macrolactone compounds

Publications (2)

Publication Number Publication Date
JPS53141289A JPS53141289A (en) 1978-12-08
JPS6236033B2 true JPS6236033B2 (enrdf_load_stackoverflow) 1987-08-05

Family

ID=12990029

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5512577A Granted JPS53141289A (en) 1977-03-09 1977-05-12 Novel macrolactone compounds

Country Status (1)

Country Link
JP (1) JPS53141289A (enrdf_load_stackoverflow)

Also Published As

Publication number Publication date
JPS53141289A (en) 1978-12-08

Similar Documents

Publication Publication Date Title
US4196280A (en) Novel macrolactone derivatives and process of producing them
EP2393779B1 (en) Process for the synthesis of cleistanthin
Nicolaou et al. Total Synthesis of Everninomicin 13,384‐1—Part 2: Synthesis of the FGHA2 Fragment
Shing et al. Catalytic asymmetric epoxidation of alkenes with arabinose-derived uloses
US5066645A (en) Epipodophyllotoxin altroside derivatives
EP0107486A1 (en) Aminonaphthacene derivatives and their production
Kinoshita et al. An enantiospecific synthesis of the C-21-C-37 segment of the aglycon of amphotericin B.
KAMETANI et al. Stereoselective synthesis of 26, 27-bisnorbrassinolide
EP0202111B1 (en) Antibacterial mycaminosyl tylonolide derivatives and their production
JPS6236033B2 (enrdf_load_stackoverflow)
JP3063943B2 (ja) 血漿中において抗菌活性の持続する新規16員環マクロリド誘導体及びその合成中間体とそれらの製造法
Tanaka et al. Syntheses of recyclized macrolide antibiotics and related derivatives from mycaminosyltylonolide.
JPH058179B2 (enrdf_load_stackoverflow)
US4255564A (en) Novel macrolactone derivatives and process of producing them
Faizullina et al. Synthesis of Nonano-9-lactone Fused to a δ-Lactone Ring
Zou et al. A novel approach to the taxane ABC ring system through chemical conversion from C19-diterpenoid alkaloid deltaline
HU180298B (en) Process for preparing new glycoside compunds
HAYASHI et al. Studies on the constituents of Asclepiadaceae Plants. XXXIV. Chemistry of sarcostin
Connolly et al. Tetranortriterpenoids. Part XVI. Partial syntheses of andirobin, methyl angolensate, mexicanolide, and 1-deoxymexicanolide
Cross et al. Steroids CCLXXX. biologically-active labile ethers v. substituted tetrahydropyran-2-yl ethers of 17β-hydroxy-2α-methyi,-5α-androstan-3-one
Matsumoto et al. The synthesis of (15R)-coleon C and (15S)-coleon C.
Matsumoto et al. The C (1)–C (10) Bond Cleavage and B Ring Aromatization of Some 6-Hydroxy-5β H-abieta-6, 8, 11, 13-tetraen-18-oic Acid 18, 6-Lactones
US6841665B2 (en) Method for synthesizing 5β, 6β-epoxides of steroids by a highly β-selective epoxidation of ΔΔ5-unsaturated steroids catalyzed by ketones
FUJITA et al. Terpenoids. XXXIII. Chemical conversion of enmein into enmelol
Cuny Synthesis of analogues of (+)-gomphoside, a potent HIF-1 inhibitor and cardenolide