ChemInform Abstract: CHIRAL SYNTHESIS OF POLYKETIDE-DERIVED NATURAL PRODUCTS. PART 5. SYNTHESIS OF F A CHIRAL SEGMENT CORRESPONDING TO THE C-1-C-5 UNIT OF ERYTHROMYCIN A FROM D-GLUCOSE

Y. OIKAWA; T. NISHI; O. YONEMITSU

doi:10.1002/chin.198517314

ChemInform Abstract: CHIRAL SYNTHESIS OF POLYKETIDE-DERIVED NATURAL PRODUCTS. PART 5. SYNTHESIS OF F A CHIRAL SEGMENT CORRESPONDING TO THE C-1-C-5 UNIT OF ERYTHROMYCIN A FROM D-GLUCOSE

Chemischer Informationsdienst ◽

10.1002/chin.198517314 ◽

1985 ◽

Vol 16 (17) ◽

Author(s):

Y. OIKAWA ◽

T. NISHI ◽

O. YONEMITSU

Keyword(s):

Natural Products ◽

Chiral Synthesis ◽

Erythromycin A

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ChemInform Abstract: CHIRAL SYNTHESIS OF POLYKETIDE-DERIVED NATURAL PRODUCTS. PART 4. SYNTHESIS OF F A LEFT-HAND SEGMENT WITH SIX CONSECUTIVE CHIRAL CENTERS OF DIHYDROERYTHRONOLIDE A FOR THE TOTAL SYNTHESIS OF ERYTHROMYCIN A FROM D-GLUCOSE

Chemischer Informationsdienst ◽

10.1002/chin.198517313 ◽

1985 ◽

Vol 16 (17) ◽

Author(s):

Y. OIKAWA ◽

T. NISHI ◽

O. YONEMITSU

Keyword(s):

Natural Products ◽

Total Synthesis ◽

Chiral Synthesis ◽

Left Hand ◽

Chiral Centers ◽

Erythromycin A

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Chiral synthesis of polyketide-derived natural products. Part 6. Chemical correlation of chiral synthons, derived from D-glucose for the synthesis of erythromycin A, with chemical cleavage products the natural antibiotic

Journal of the Chemical Society Perkin Transactions 1 ◽

10.1039/p19850000027 ◽

1985 ◽

pp. 27 ◽

Cited By ~ 2

Author(s):

Yuji Oikawa ◽

Takao Nishi ◽

Osamu Yonemitsu

Keyword(s):

Natural Products ◽

Chiral Synthesis ◽

Chemical Cleavage ◽

Chemical Correlation ◽

Erythromycin A

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Chiral synthesis of polyketide-derived natural products. Part 3. Stereocontrolled synthesis of a chiral fragment corresponding to both the C-1—C-4 and C-9—C-12 units of erythromycin A fromD-glucose

Journal of the Chemical Society Perkin Transactions 1 ◽

10.1039/p19850000001 ◽

1985 ◽

pp. 1-5 ◽

Cited By ~ 4

Author(s):

Yuji Oikawa ◽

Takao Nishi ◽

Osamu Yonemitsu

Keyword(s):

Natural Products ◽

Chiral Synthesis ◽

Stereocontrolled Synthesis ◽

Erythromycin A

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Chiral synthesis of polyketide-derived natural products. Part 4. Synthesis of a left-hand segment with six consecutive chiral centres of dihydroerythronolide A for the total synthesis of erythromycin A from D-glucose

Journal of the Chemical Society Perkin Transactions 1 ◽

10.1039/p19850000007 ◽

1985 ◽

pp. 7 ◽

Cited By ~ 14

Author(s):

Yuji Oikawa ◽

Takao Nishi ◽

Osamu Yonemitsu

Keyword(s):

Natural Products ◽

Total Synthesis ◽

Chiral Synthesis ◽

Left Hand ◽

Erythromycin A

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Chiral synthesis of polyketide-derived natural products. Part 5. Synthesis of a chiral segment corresponding to the C-1—C-5 unit of erythromycin A fromD-glucose

Journal of the Chemical Society Perkin Transactions 1 ◽

10.1039/p19850000019 ◽

1985 ◽

pp. 19-26 ◽

Cited By ~ 3

Author(s):

Yuji Oikawa ◽

Takao Nishi ◽

Osamu Yonemitsu

Keyword(s):

Natural Products ◽

Chiral Synthesis ◽

Erythromycin A

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ChemInform Abstract: CHIRAL SYNTHESIS OF POLYKETIDE-DERIVED NATURAL PRODUCTS. PART 6. CHEMICAL CORRELATION OF CHIRAL SYNTHONS DERIVED FROM D-GLUCOSE FOR THE SYNTHESIS OF ERYTHROMYCIN A, WITH CHEMICAL CLEAVAGE PRODUCTS OF THE NATURAL ANTIBIOTIC

Chemischer Informationsdienst ◽

10.1002/chin.198517315 ◽

1985 ◽

Vol 16 (17) ◽

Author(s):

Y. OIKAWA ◽

T. NISHI ◽

O. YONEMITSU

Keyword(s):

Natural Products ◽

Chiral Synthesis ◽

Chemical Cleavage ◽

Chemical Correlation ◽

Erythromycin A

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ChemInform Abstract: CHIRAL SYNTHESIS OF POLYKETIDE-DERIVED NATURAL PRODUCTS. 2. STEREOCONTROLLED SYNTHESIS OF A SEGMENT HAVING SIX CONSECUTIVE CHIRAL CENTERS FOR THE SYNTHESIS OF ERYTHROMYCIN A FROM D-GLUCOSE

Chemischer Informationsdienst ◽

10.1002/chin.198352349 ◽

1983 ◽

Vol 14 (52) ◽

Author(s):

Y. OIKAWA ◽

T. NISHI ◽

O. YONEMITSU

Keyword(s):

Natural Products ◽

Chiral Synthesis ◽

Stereocontrolled Synthesis ◽

Chiral Centers ◽

Erythromycin A

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ChemInform Abstract: CHIRAL SYNTHESIS OF POLYKETIDE-DERIVED NATURAL PRODUCTS. PART 3. STEREOCONTROLLED SYNTHESIS OF A CHIRAL FRAGMENT CORRESPONDING TO BOTH THE C-1-C-4 AND C-9-C-12 UNITS OF ERYTHROMYCIN A FROM D-GLUCOSE

Chemischer Informationsdienst ◽

10.1002/chin.198517312 ◽

1985 ◽

Vol 16 (17) ◽

Author(s):

Y. OIKAWA ◽

T. NISHI ◽

O. YONEMITSU

Keyword(s):

Natural Products ◽

Chiral Synthesis ◽

Stereocontrolled Synthesis ◽

Erythromycin A

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Chiral synthesis of polyketide-derived natural products. 44. Large Laboratory scale Synthesis of (2S,3S)-2-(4-Methoxybenzyloxy)-3,4-O-(3-pentylidene)-1,3,4-butantriol, a Versatile Chiral Building Block in Natural Product Synthesis.

Chemical and Pharmaceutical Bulletin ◽

10.1248/cpb.42.683 ◽

1994 ◽

Vol 42 (3) ◽

pp. 683-685 ◽

Cited By ~ 4

Author(s):

Kiyoshi HORITA ◽

Youji SAKURAI ◽

Shun-ichiro HACHIYA ◽

Masaaki NAGASAWA ◽

Osamu YONEMITSU

Keyword(s):

Natural Products ◽

Natural Product ◽

Building Block ◽

Laboratory Scale ◽

Natural Product Synthesis ◽

Chiral Synthesis ◽

Chiral Building Block

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ChemInform Abstract: Chiral Synthesis of Polyketide-Derived Natural Products. Part 10. Stereoselective Synthesis of Pikronolide, the Aglycon of the 14-Membered Ring Macrolide Pikromycin, from D-Glucose. Role of MPM and DMPM Protection.

Chemischer Informationsdienst ◽

10.1002/chin.198648346 ◽

1986 ◽

Vol 17 (48) ◽

Author(s):

N. NAKAJIMA ◽

T. HAMADA ◽

T. TANAKA ◽

Y. OIKAWA ◽

O. YONEMITSU

Keyword(s):

Natural Products ◽

Stereoselective Synthesis ◽

Membered Ring ◽

Chiral Synthesis

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