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Volumn 23, Issue 32, 1982, Pages 3301-3304

Transfer of functionalized carbon fragments via substituted 5, 10-methylentetetrahydrofolate models. Approach to dihydroindole and indole alkaloids.

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0003801180 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(00)87598-X Document Type: Article

Times cited : (13)

References (14)

1
- 0018852667
- On the Mechanism of Action of Folate-And Biopterin-Requiring Enzymes
- (1980) Annual Review of Biochemistry , vol.49 , pp. 229
- Benkovic¹

3
- 33745354186
- Carbon Transfer via N5, N1 0-Methylenetetrahydrofolate Models
- (1979) HETEROCYCLES , vol.13 , pp. 221
- Bieräugel¹ Plemp² Hiemstra³ Pandit⁴

4
- 33745355010
- Trnsfer of a Functionalized Carbon-fragment via a (Substituted) N5,N10-Methylenetetrahydrofolic Acid Model. An Approach to D,L-Pyridindolol
- (1980) HETEROCYCLES , vol.14 , pp. 947
- Bieräugel¹ Plemp² Pandit³

5
- 33745423998
- A Two Synthon Approach to D15,17,19-Yohimbane Skeleton via a N5,N10-Methylenetetrahydrofolate Model. A Facile Route to b-Carboline Alkaloids
- (1981) HETEROCYCLES , vol.16 , pp. 239
- Bieräugel¹ Hiemstra² Pandit³

7
- 84918344359
- 3a,b were converted to 4a,b upon mild treatment with acid or base.

8
- 84918344358
- The Z-configuration of 5a,b was attested by the coupling constants of the vinylic protons. (5a J = 7 Hz, 5b J = 7 Hz).

9
- 84918344357
- 6): δ 4.20 [1H, 2, C(2)-H], 3.43 [1H, dxd J = 12 Hz, J = 4Hz, C(21)-H]. Details of the NMR spectra and the NOE experiments shall be presented elsewhere.

10
- 84918344356
- The numbering system used is one based on a biogenetic interrelationship of indole alkaloids as proposed by J. LeMen and Taylor, Experientia 21, 508 (1965)

11
- 0015245566
- Total synthesis of (+-)-vindorosine
- (1971) Journal of the American Chemical Society , vol.93 , pp. 3299
- Büchi¹ Matsumoto² Nishimura³

12
- 33847801572
- (1975) J. Am. Chem. Soc. , vol.97 , pp. 6880
- Ando¹ Büchi² Ohnuma³

13
- 31044453693
- Two Facile Routes to the Intermediates for the Syntheses of Aspidosperma Indole Alkaloids, Vindoline and Vindorosine
- (1977) HETEROCYCLES , vol.6 , pp. 1699
- Takano¹ Shishido² Sato³ Ogasawara⁴

14
- 84918344355
- Mechanistic aspects of the formation of 7 shall be discussed in a forthcoming paper.

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